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You searched for subject:(Heck reaction). Showing records 1 – 30 of 74 total matches.

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Universidade Estadual de Campinas

1. Silva, Allan Ribeiro da, 1989-. Reações de oxa-Heck-Matsuda enantiosseletivas envolvendo sistemas estirênicos : síntese enantiosseletiva de sistemas trans-diidrobenzofuranos substituídos e síntese total da neolignana natural (-)-conocarpano: Enantioselective oxy-Heck-Matsuda arylation in styrenic system : enantioselective synthesis of substituted trans-dihydrobenzofuram system and total synthesis of the neolignan (-)-conocarpan.

Degree: 2017, Universidade Estadual de Campinas

 Abstract: The formation of C-C bonds in an enantioselective manner is of crucial importance in organic synthesis. In this regard, the enantioselective Heck¿Matsuda reaction is… (more)

Subjects/Keywords: Heck-Matsuda, reação de; Sais de diazônio; Heck-Matsuda enantiosseletiva; Heck-Matsuda reaction; Diazonium salts; Enantioselective Heck-Matsuda

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Silva, Allan Ribeiro da, 1. (2017). Reações de oxa-Heck-Matsuda enantiosseletivas envolvendo sistemas estirênicos : síntese enantiosseletiva de sistemas trans-diidrobenzofuranos substituídos e síntese total da neolignana natural (-)-conocarpano: Enantioselective oxy-Heck-Matsuda arylation in styrenic system : enantioselective synthesis of substituted trans-dihydrobenzofuram system and total synthesis of the neolignan (-)-conocarpan. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/330757

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Silva, Allan Ribeiro da, 1989-. “Reações de oxa-Heck-Matsuda enantiosseletivas envolvendo sistemas estirênicos : síntese enantiosseletiva de sistemas trans-diidrobenzofuranos substituídos e síntese total da neolignana natural (-)-conocarpano: Enantioselective oxy-Heck-Matsuda arylation in styrenic system : enantioselective synthesis of substituted trans-dihydrobenzofuram system and total synthesis of the neolignan (-)-conocarpan.” 2017. Thesis, Universidade Estadual de Campinas. Accessed March 06, 2021. http://repositorio.unicamp.br/jspui/handle/REPOSIP/330757.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Silva, Allan Ribeiro da, 1989-. “Reações de oxa-Heck-Matsuda enantiosseletivas envolvendo sistemas estirênicos : síntese enantiosseletiva de sistemas trans-diidrobenzofuranos substituídos e síntese total da neolignana natural (-)-conocarpano: Enantioselective oxy-Heck-Matsuda arylation in styrenic system : enantioselective synthesis of substituted trans-dihydrobenzofuram system and total synthesis of the neolignan (-)-conocarpan.” 2017. Web. 06 Mar 2021.

Vancouver:

Silva, Allan Ribeiro da 1. Reações de oxa-Heck-Matsuda enantiosseletivas envolvendo sistemas estirênicos : síntese enantiosseletiva de sistemas trans-diidrobenzofuranos substituídos e síntese total da neolignana natural (-)-conocarpano: Enantioselective oxy-Heck-Matsuda arylation in styrenic system : enantioselective synthesis of substituted trans-dihydrobenzofuram system and total synthesis of the neolignan (-)-conocarpan. [Internet] [Thesis]. Universidade Estadual de Campinas; 2017. [cited 2021 Mar 06]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/330757.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Silva, Allan Ribeiro da 1. Reações de oxa-Heck-Matsuda enantiosseletivas envolvendo sistemas estirênicos : síntese enantiosseletiva de sistemas trans-diidrobenzofuranos substituídos e síntese total da neolignana natural (-)-conocarpano: Enantioselective oxy-Heck-Matsuda arylation in styrenic system : enantioselective synthesis of substituted trans-dihydrobenzofuram system and total synthesis of the neolignan (-)-conocarpan. [Thesis]. Universidade Estadual de Campinas; 2017. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/330757

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université de Bordeaux I

2. Nassar Hardy, Luma. Tandem reactions using multi-task catalysts : Réaction en tandem par catalyse hétérogène.

Degree: Docteur es, Chimie organique, 2011, Université de Bordeaux I

Le développement d’une chimie propre et donc durable est un des challenges majeurs du 21ème siècle dans les pays industrialisés. Étant au cœur de nombreuses… (more)

Subjects/Keywords: Reaction de Heck-Matsuda; Reaction de Heck; Sel de diazonium; One-pot; HRC strategy; Heck reaction; Heck-Matsuda reaction; Diazonium salt; One- pot; HRC strategy

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APA (6th Edition):

Nassar Hardy, L. (2011). Tandem reactions using multi-task catalysts : Réaction en tandem par catalyse hétérogène. (Doctoral Dissertation). Université de Bordeaux I. Retrieved from http://www.theses.fr/2011BOR14317

Chicago Manual of Style (16th Edition):

Nassar Hardy, Luma. “Tandem reactions using multi-task catalysts : Réaction en tandem par catalyse hétérogène.” 2011. Doctoral Dissertation, Université de Bordeaux I. Accessed March 06, 2021. http://www.theses.fr/2011BOR14317.

MLA Handbook (7th Edition):

Nassar Hardy, Luma. “Tandem reactions using multi-task catalysts : Réaction en tandem par catalyse hétérogène.” 2011. Web. 06 Mar 2021.

Vancouver:

Nassar Hardy L. Tandem reactions using multi-task catalysts : Réaction en tandem par catalyse hétérogène. [Internet] [Doctoral dissertation]. Université de Bordeaux I; 2011. [cited 2021 Mar 06]. Available from: http://www.theses.fr/2011BOR14317.

Council of Science Editors:

Nassar Hardy L. Tandem reactions using multi-task catalysts : Réaction en tandem par catalyse hétérogène. [Doctoral Dissertation]. Université de Bordeaux I; 2011. Available from: http://www.theses.fr/2011BOR14317


University of Delaware

3. McAtee, Jesse Ryan. Development of the first and second-generation Silyl-Heck reactions.

Degree: PhD, University of Delaware, Department of Chemistry and Biochemistry, 2015, University of Delaware

 Allyl and vinylsilanes are important nucleophiles in organic synthesis. They are stable reagents that can participate in a variety of transformations including mainly Hosomi-Sakurai crotylations,… (more)

Subjects/Keywords: Heck reaction.; Silane compounds.; Ligands.; Catalysis.

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APA (6th Edition):

McAtee, J. R. (2015). Development of the first and second-generation Silyl-Heck reactions. (Doctoral Dissertation). University of Delaware. Retrieved from http://udspace.udel.edu/handle/19716/17487

Chicago Manual of Style (16th Edition):

McAtee, Jesse Ryan. “Development of the first and second-generation Silyl-Heck reactions.” 2015. Doctoral Dissertation, University of Delaware. Accessed March 06, 2021. http://udspace.udel.edu/handle/19716/17487.

MLA Handbook (7th Edition):

McAtee, Jesse Ryan. “Development of the first and second-generation Silyl-Heck reactions.” 2015. Web. 06 Mar 2021.

Vancouver:

McAtee JR. Development of the first and second-generation Silyl-Heck reactions. [Internet] [Doctoral dissertation]. University of Delaware; 2015. [cited 2021 Mar 06]. Available from: http://udspace.udel.edu/handle/19716/17487.

Council of Science Editors:

McAtee JR. Development of the first and second-generation Silyl-Heck reactions. [Doctoral Dissertation]. University of Delaware; 2015. Available from: http://udspace.udel.edu/handle/19716/17487


University of Illinois – Chicago

4. Parasram, Marvin. Development of Heck and Desaturation Reactions Involving Novel Hybrid Palladium-Radical Intermediates.

Degree: 2017, University of Illinois – Chicago

 The first part of the thesis focuses on the development of the first endo-selective Pd-catalyzed Heck reaction of iodomethylsilyl ethers of phenols and alkenols leading… (more)

Subjects/Keywords: Heck reaction; Desaturation; C–H Functionalization

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APA (6th Edition):

Parasram, M. (2017). Development of Heck and Desaturation Reactions Involving Novel Hybrid Palladium-Radical Intermediates. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/22205

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Parasram, Marvin. “Development of Heck and Desaturation Reactions Involving Novel Hybrid Palladium-Radical Intermediates.” 2017. Thesis, University of Illinois – Chicago. Accessed March 06, 2021. http://hdl.handle.net/10027/22205.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Parasram, Marvin. “Development of Heck and Desaturation Reactions Involving Novel Hybrid Palladium-Radical Intermediates.” 2017. Web. 06 Mar 2021.

Vancouver:

Parasram M. Development of Heck and Desaturation Reactions Involving Novel Hybrid Palladium-Radical Intermediates. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10027/22205.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Parasram M. Development of Heck and Desaturation Reactions Involving Novel Hybrid Palladium-Radical Intermediates. [Thesis]. University of Illinois – Chicago; 2017. Available from: http://hdl.handle.net/10027/22205

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universidade Estadual de Campinas

5. Prediger, Patrícia, 1984-. Reações de arilação de Heck com sais de arenodiazônio : estudos metodológicos e aplicações nas sínteses de compostos bioativos: Heck arylations with arenediazonium salts : methodological studies and application on bioactive compounds synthesis.

Degree: 2012, Universidade Estadual de Campinas

 Abstract: The present work was focused in the Heck-Matsuda arylation of several olefins with arenediazonium salts and in the application of the arylated products as… (more)

Subjects/Keywords: Reação de Heck; Alilaminas; Sais de arenodiazônio; Paládio; Heck reaction; Allylamines; Arenediazonium salts; Palladium

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APA (6th Edition):

Prediger, Patrícia, 1. (2012). Reações de arilação de Heck com sais de arenodiazônio : estudos metodológicos e aplicações nas sínteses de compostos bioativos: Heck arylations with arenediazonium salts : methodological studies and application on bioactive compounds synthesis. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/249886

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Prediger, Patrícia, 1984-. “Reações de arilação de Heck com sais de arenodiazônio : estudos metodológicos e aplicações nas sínteses de compostos bioativos: Heck arylations with arenediazonium salts : methodological studies and application on bioactive compounds synthesis.” 2012. Thesis, Universidade Estadual de Campinas. Accessed March 06, 2021. http://repositorio.unicamp.br/jspui/handle/REPOSIP/249886.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Prediger, Patrícia, 1984-. “Reações de arilação de Heck com sais de arenodiazônio : estudos metodológicos e aplicações nas sínteses de compostos bioativos: Heck arylations with arenediazonium salts : methodological studies and application on bioactive compounds synthesis.” 2012. Web. 06 Mar 2021.

Vancouver:

Prediger, Patrícia 1. Reações de arilação de Heck com sais de arenodiazônio : estudos metodológicos e aplicações nas sínteses de compostos bioativos: Heck arylations with arenediazonium salts : methodological studies and application on bioactive compounds synthesis. [Internet] [Thesis]. Universidade Estadual de Campinas; 2012. [cited 2021 Mar 06]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/249886.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Prediger, Patrícia 1. Reações de arilação de Heck com sais de arenodiazônio : estudos metodológicos e aplicações nas sínteses de compostos bioativos: Heck arylations with arenediazonium salts : methodological studies and application on bioactive compounds synthesis. [Thesis]. Universidade Estadual de Campinas; 2012. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/249886

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universiteit Utrecht

6. Huang, Y. Practical catalytic arylation of C–H bonds by iron/phenanthroline systems.

Degree: 2015, Universiteit Utrecht

 In Chapter 1, an overview is given of the current status of the field of non-precious metal catalyzed/mediated direct arylation reactions. Reports on direct arylations… (more)

Subjects/Keywords: iron; direct arylation; air tolerant; kinetic study; Heck reaction; radical

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APA (6th Edition):

Huang, Y. (2015). Practical catalytic arylation of C–H bonds by iron/phenanthroline systems. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/324941

Chicago Manual of Style (16th Edition):

Huang, Y. “Practical catalytic arylation of C–H bonds by iron/phenanthroline systems.” 2015. Doctoral Dissertation, Universiteit Utrecht. Accessed March 06, 2021. http://dspace.library.uu.nl:8080/handle/1874/324941.

MLA Handbook (7th Edition):

Huang, Y. “Practical catalytic arylation of C–H bonds by iron/phenanthroline systems.” 2015. Web. 06 Mar 2021.

Vancouver:

Huang Y. Practical catalytic arylation of C–H bonds by iron/phenanthroline systems. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2015. [cited 2021 Mar 06]. Available from: http://dspace.library.uu.nl:8080/handle/1874/324941.

Council of Science Editors:

Huang Y. Practical catalytic arylation of C–H bonds by iron/phenanthroline systems. [Doctoral Dissertation]. Universiteit Utrecht; 2015. Available from: http://dspace.library.uu.nl:8080/handle/1874/324941


University of Johannesburg

7. Tshivhase, Mmboneni Gifty. Functionalised porphyrazines and their use in catalysis.

Degree: 2012, University of Johannesburg

D.Phil.

Porphyrazines like porphyrins and phthalocyanines have unique physical, chemical and spectral properties. This allows them to have many impressive applications. They are less studied… (more)

Subjects/Keywords: Catalysis; Porphyrins; Phthalocyanines; Palladium compounds; Heck reaction; Imidazoles; Ligands

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APA (6th Edition):

Tshivhase, M. G. (2012). Functionalised porphyrazines and their use in catalysis. (Thesis). University of Johannesburg. Retrieved from http://hdl.handle.net/10210/6024

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Tshivhase, Mmboneni Gifty. “Functionalised porphyrazines and their use in catalysis.” 2012. Thesis, University of Johannesburg. Accessed March 06, 2021. http://hdl.handle.net/10210/6024.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Tshivhase, Mmboneni Gifty. “Functionalised porphyrazines and their use in catalysis.” 2012. Web. 06 Mar 2021.

Vancouver:

Tshivhase MG. Functionalised porphyrazines and their use in catalysis. [Internet] [Thesis]. University of Johannesburg; 2012. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10210/6024.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Tshivhase MG. Functionalised porphyrazines and their use in catalysis. [Thesis]. University of Johannesburg; 2012. Available from: http://hdl.handle.net/10210/6024

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Johannesburg

8. Yankey, Margaret. Imidazolyl- and pyrazolyl-salicylaldimine transition metal complexes and their applications in olefin transformation reactions.

Degree: 2011, University of Johannesburg

M.Sc.

This study deals with the synthesis of nitrogen-donor imidazolyl- and pyrazolyl-salicylaldimine compounds, their reactions with selected transition metals and applications as catalysts for Heck(more)

Subjects/Keywords: Salicylates; Transition metal complexes; Alkenes; Catalysts; Heck reaction; Ligands

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APA (6th Edition):

Yankey, M. (2011). Imidazolyl- and pyrazolyl-salicylaldimine transition metal complexes and their applications in olefin transformation reactions. (Thesis). University of Johannesburg. Retrieved from http://hdl.handle.net/10210/3627

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Yankey, Margaret. “Imidazolyl- and pyrazolyl-salicylaldimine transition metal complexes and their applications in olefin transformation reactions.” 2011. Thesis, University of Johannesburg. Accessed March 06, 2021. http://hdl.handle.net/10210/3627.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Yankey, Margaret. “Imidazolyl- and pyrazolyl-salicylaldimine transition metal complexes and their applications in olefin transformation reactions.” 2011. Web. 06 Mar 2021.

Vancouver:

Yankey M. Imidazolyl- and pyrazolyl-salicylaldimine transition metal complexes and their applications in olefin transformation reactions. [Internet] [Thesis]. University of Johannesburg; 2011. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10210/3627.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Yankey M. Imidazolyl- and pyrazolyl-salicylaldimine transition metal complexes and their applications in olefin transformation reactions. [Thesis]. University of Johannesburg; 2011. Available from: http://hdl.handle.net/10210/3627

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Toronto

9. Schulman, Jacqueline Madeleine. Synthesis of 1,2,3-Triazole-fused Heterocycles via Palladium Catalyzed Annulation of 5-Iodotriazoles.

Degree: 2011, University of Toronto

Increasing attention has recently been directed toward 1,2,3-triazole-containing compounds. With their unique properties and excellent stability, 1,4-disubstituted triazoles are readily accessible via the copper catalyzed… (more)

Subjects/Keywords: triazoles; palladium catalysis; Heck reaction; dirct arylation; organic chemistry; 0490

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APA (6th Edition):

Schulman, J. M. (2011). Synthesis of 1,2,3-Triazole-fused Heterocycles via Palladium Catalyzed Annulation of 5-Iodotriazoles. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/31434

Chicago Manual of Style (16th Edition):

Schulman, Jacqueline Madeleine. “Synthesis of 1,2,3-Triazole-fused Heterocycles via Palladium Catalyzed Annulation of 5-Iodotriazoles.” 2011. Masters Thesis, University of Toronto. Accessed March 06, 2021. http://hdl.handle.net/1807/31434.

MLA Handbook (7th Edition):

Schulman, Jacqueline Madeleine. “Synthesis of 1,2,3-Triazole-fused Heterocycles via Palladium Catalyzed Annulation of 5-Iodotriazoles.” 2011. Web. 06 Mar 2021.

Vancouver:

Schulman JM. Synthesis of 1,2,3-Triazole-fused Heterocycles via Palladium Catalyzed Annulation of 5-Iodotriazoles. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1807/31434.

Council of Science Editors:

Schulman JM. Synthesis of 1,2,3-Triazole-fused Heterocycles via Palladium Catalyzed Annulation of 5-Iodotriazoles. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/31434


University of Newcastle

10. Al Otaibi, Ahmed Abdullah. Application of green chemistry approaches to cytotoxic compounds.

Degree: PhD, 2018, University of Newcastle

Research Doctorate - Doctor of Philosophy (PhD)

The specific synthesis of organic compounds requires careful control of reaction parameters conditions, such as temperatures, pressure and… (more)

Subjects/Keywords: ionic liquids; cytotoxic compounds; heck reaction; flow chemistry

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APA (6th Edition):

Al Otaibi, A. A. (2018). Application of green chemistry approaches to cytotoxic compounds. (Doctoral Dissertation). University of Newcastle. Retrieved from http://hdl.handle.net/1959.13/1383620

Chicago Manual of Style (16th Edition):

Al Otaibi, Ahmed Abdullah. “Application of green chemistry approaches to cytotoxic compounds.” 2018. Doctoral Dissertation, University of Newcastle. Accessed March 06, 2021. http://hdl.handle.net/1959.13/1383620.

MLA Handbook (7th Edition):

Al Otaibi, Ahmed Abdullah. “Application of green chemistry approaches to cytotoxic compounds.” 2018. Web. 06 Mar 2021.

Vancouver:

Al Otaibi AA. Application of green chemistry approaches to cytotoxic compounds. [Internet] [Doctoral dissertation]. University of Newcastle; 2018. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1959.13/1383620.

Council of Science Editors:

Al Otaibi AA. Application of green chemistry approaches to cytotoxic compounds. [Doctoral Dissertation]. University of Newcastle; 2018. Available from: http://hdl.handle.net/1959.13/1383620


University of Oxford

11. Baker, David Bawden. Applications of the Heck reaction for the syntheses of substituted pyridines and β,β-disubstituted vinyl Weinreb amides : studies towards the syntheses of inthomycin B and inthomycin C.

Degree: PhD, 2014, University of Oxford

 The Heck reaction has become a fundamental reaction for synthetic organic chemists over the last half century and is utilised heavily in the fine chemical… (more)

Subjects/Keywords: 547; Organic chemistry; Organic synthesis; Synthetic organic chemistry; Heck reaction; Pyridines

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APA (6th Edition):

Baker, D. B. (2014). Applications of the Heck reaction for the syntheses of substituted pyridines and β,β-disubstituted vinyl Weinreb amides : studies towards the syntheses of inthomycin B and inthomycin C. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:09765f4e-83b9-4bb6-9130-7da3520752e6 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627840

Chicago Manual of Style (16th Edition):

Baker, David Bawden. “Applications of the Heck reaction for the syntheses of substituted pyridines and β,β-disubstituted vinyl Weinreb amides : studies towards the syntheses of inthomycin B and inthomycin C.” 2014. Doctoral Dissertation, University of Oxford. Accessed March 06, 2021. http://ora.ox.ac.uk/objects/uuid:09765f4e-83b9-4bb6-9130-7da3520752e6 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627840.

MLA Handbook (7th Edition):

Baker, David Bawden. “Applications of the Heck reaction for the syntheses of substituted pyridines and β,β-disubstituted vinyl Weinreb amides : studies towards the syntheses of inthomycin B and inthomycin C.” 2014. Web. 06 Mar 2021.

Vancouver:

Baker DB. Applications of the Heck reaction for the syntheses of substituted pyridines and β,β-disubstituted vinyl Weinreb amides : studies towards the syntheses of inthomycin B and inthomycin C. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2021 Mar 06]. Available from: http://ora.ox.ac.uk/objects/uuid:09765f4e-83b9-4bb6-9130-7da3520752e6 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627840.

Council of Science Editors:

Baker DB. Applications of the Heck reaction for the syntheses of substituted pyridines and β,β-disubstituted vinyl Weinreb amides : studies towards the syntheses of inthomycin B and inthomycin C. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:09765f4e-83b9-4bb6-9130-7da3520752e6 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627840


Iowa State University

12. Kadam, Abhishek Ashok. Catalytic methods for alkene functionalization reactions.

Degree: 2019, Iowa State University

 This thesis presents the efforts towards developing transition metal-catalyzed protocols for rapid functionalization of alkenes. These protocols include - 1) enantioselective, palladium-catalyzed conjugate additions of… (more)

Subjects/Keywords: carboacylation; conjugate addition; heck reaction; nickel; palladium; triphenylborane; Organic Chemistry

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APA (6th Edition):

Kadam, A. A. (2019). Catalytic methods for alkene functionalization reactions. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/17712

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kadam, Abhishek Ashok. “Catalytic methods for alkene functionalization reactions.” 2019. Thesis, Iowa State University. Accessed March 06, 2021. https://lib.dr.iastate.edu/etd/17712.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kadam, Abhishek Ashok. “Catalytic methods for alkene functionalization reactions.” 2019. Web. 06 Mar 2021.

Vancouver:

Kadam AA. Catalytic methods for alkene functionalization reactions. [Internet] [Thesis]. Iowa State University; 2019. [cited 2021 Mar 06]. Available from: https://lib.dr.iastate.edu/etd/17712.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kadam AA. Catalytic methods for alkene functionalization reactions. [Thesis]. Iowa State University; 2019. Available from: https://lib.dr.iastate.edu/etd/17712

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Illinois – Urbana-Champaign

13. Delcamp, Jared H. Oxidative Heck Reactions with Terminal Olefins.

Degree: PhD, 0335, 2011, University of Illinois – Urbana-Champaign

 Sequential transformations in a single reaction have the potential to dramatically increase efficiency with respect to resources, time, and number of steps to access key… (more)

Subjects/Keywords: Heck reaction; oxidative; Palladium; arylation; vinylation; transition metal catalysis

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Delcamp, J. H. (2011). Oxidative Heck Reactions with Terminal Olefins. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/18626

Chicago Manual of Style (16th Edition):

Delcamp, Jared H. “Oxidative Heck Reactions with Terminal Olefins.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed March 06, 2021. http://hdl.handle.net/2142/18626.

MLA Handbook (7th Edition):

Delcamp, Jared H. “Oxidative Heck Reactions with Terminal Olefins.” 2011. Web. 06 Mar 2021.

Vancouver:

Delcamp JH. Oxidative Heck Reactions with Terminal Olefins. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/2142/18626.

Council of Science Editors:

Delcamp JH. Oxidative Heck Reactions with Terminal Olefins. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/18626


University of Iowa

14. Joshi, Madhur Satish. Elaboration of azine and azole anhydrobases via intra- and intermolecular cyclizations for heterocycle construction.

Degree: PhD, Chemistry, 2017, University of Iowa

  Aza-heterocycles such as pyridines, imidazoles, piperidines, etc. are ubiquitous structural motifs found in various natural products and pharmacologically active compounds. Thus, they are of… (more)

Subjects/Keywords: Anhydrobases; Aza-heterocycles; Heck reaction; Pyridines; Triazoles; Chemistry

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APA (6th Edition):

Joshi, M. S. (2017). Elaboration of azine and azole anhydrobases via intra- and intermolecular cyclizations for heterocycle construction. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/5788

Chicago Manual of Style (16th Edition):

Joshi, Madhur Satish. “Elaboration of azine and azole anhydrobases via intra- and intermolecular cyclizations for heterocycle construction.” 2017. Doctoral Dissertation, University of Iowa. Accessed March 06, 2021. https://ir.uiowa.edu/etd/5788.

MLA Handbook (7th Edition):

Joshi, Madhur Satish. “Elaboration of azine and azole anhydrobases via intra- and intermolecular cyclizations for heterocycle construction.” 2017. Web. 06 Mar 2021.

Vancouver:

Joshi MS. Elaboration of azine and azole anhydrobases via intra- and intermolecular cyclizations for heterocycle construction. [Internet] [Doctoral dissertation]. University of Iowa; 2017. [cited 2021 Mar 06]. Available from: https://ir.uiowa.edu/etd/5788.

Council of Science Editors:

Joshi MS. Elaboration of azine and azole anhydrobases via intra- and intermolecular cyclizations for heterocycle construction. [Doctoral Dissertation]. University of Iowa; 2017. Available from: https://ir.uiowa.edu/etd/5788


University of Southern California

15. Jarusiewicz, Jamie A. Synthesis of protein-protein interaction inhibitors and development of new catalytic methods.

Degree: PhD, Chemistry, 2012, University of Southern California

 This dissertation comprises three projects, two related to the synthesis and evaluation of small molecule inhibitors of protein-protein interactions, and one related to development of… (more)

Subjects/Keywords: organic synthesis; Heck reaction; Strecker reaction; N-heterocyclic carbenes; BCL-2 inhibitors; MEF2

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Jarusiewicz, J. A. (2012). Synthesis of protein-protein interaction inhibitors and development of new catalytic methods. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/80293/rec/6294

Chicago Manual of Style (16th Edition):

Jarusiewicz, Jamie A. “Synthesis of protein-protein interaction inhibitors and development of new catalytic methods.” 2012. Doctoral Dissertation, University of Southern California. Accessed March 06, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/80293/rec/6294.

MLA Handbook (7th Edition):

Jarusiewicz, Jamie A. “Synthesis of protein-protein interaction inhibitors and development of new catalytic methods.” 2012. Web. 06 Mar 2021.

Vancouver:

Jarusiewicz JA. Synthesis of protein-protein interaction inhibitors and development of new catalytic methods. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2021 Mar 06]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/80293/rec/6294.

Council of Science Editors:

Jarusiewicz JA. Synthesis of protein-protein interaction inhibitors and development of new catalytic methods. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/80293/rec/6294


Universidade Estadual de Campinas

16. Penha, Eduardo Tanoue da, 1980-. Estudo computacional do mecanismo da reação de Heck-Matsuda e aplicação sintética: Computational study of the Heck-Matsuda reaction mechanism and synthetic application.

Degree: 2015, Universidade Estadual de Campinas

 Abstract: This thesis has two subjects: the first one entitled "Mechanistic study of the Heck-Matsuda reaction", comprised a computational study of the Heck reaction using… (more)

Subjects/Keywords: Heck-Matsuda, reação de; Cálculos teóricos; 3,4-diidroisocumarina; Ftalídeo; Heck-Matsuda reaction; Theoretical calculations; 3,4-dihydroisocoumarin; Phthalide

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APA (6th Edition):

Penha, Eduardo Tanoue da, 1. (2015). Estudo computacional do mecanismo da reação de Heck-Matsuda e aplicação sintética: Computational study of the Heck-Matsuda reaction mechanism and synthetic application. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/249874

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Penha, Eduardo Tanoue da, 1980-. “Estudo computacional do mecanismo da reação de Heck-Matsuda e aplicação sintética: Computational study of the Heck-Matsuda reaction mechanism and synthetic application.” 2015. Thesis, Universidade Estadual de Campinas. Accessed March 06, 2021. http://repositorio.unicamp.br/jspui/handle/REPOSIP/249874.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Penha, Eduardo Tanoue da, 1980-. “Estudo computacional do mecanismo da reação de Heck-Matsuda e aplicação sintética: Computational study of the Heck-Matsuda reaction mechanism and synthetic application.” 2015. Web. 06 Mar 2021.

Vancouver:

Penha, Eduardo Tanoue da 1. Estudo computacional do mecanismo da reação de Heck-Matsuda e aplicação sintética: Computational study of the Heck-Matsuda reaction mechanism and synthetic application. [Internet] [Thesis]. Universidade Estadual de Campinas; 2015. [cited 2021 Mar 06]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/249874.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Penha, Eduardo Tanoue da 1. Estudo computacional do mecanismo da reação de Heck-Matsuda e aplicação sintética: Computational study of the Heck-Matsuda reaction mechanism and synthetic application. [Thesis]. Universidade Estadual de Campinas; 2015. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/249874

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universidade Estadual de Campinas

17. Carmona, Rafaela Costa, 1988-. Novas aplicações da reação de Heck enantiosseletiva : dessimetrizações e reações intramoleculares: New applications of the enantioselective Heck reaction : desymmetrizations and intramolecular reactions.

Degree: 2018, Universidade Estadual de Campinas

 Abstract: The Heck reaction is considered a very efficient method for the formation of carbon-carbon bonds and one of the most used transformations in organic… (more)

Subjects/Keywords: Catálise enantiosseletiva; Reação de Heck; Sais de arenodiazônio; Paládio; Enantioselective catalysis; Heck reaction; Arenediazonium salts; Palladium

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Carmona, Rafaela Costa, 1. (2018). Novas aplicações da reação de Heck enantiosseletiva : dessimetrizações e reações intramoleculares: New applications of the enantioselective Heck reaction : desymmetrizations and intramolecular reactions. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/331977

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Carmona, Rafaela Costa, 1988-. “Novas aplicações da reação de Heck enantiosseletiva : dessimetrizações e reações intramoleculares: New applications of the enantioselective Heck reaction : desymmetrizations and intramolecular reactions.” 2018. Thesis, Universidade Estadual de Campinas. Accessed March 06, 2021. http://repositorio.unicamp.br/jspui/handle/REPOSIP/331977.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Carmona, Rafaela Costa, 1988-. “Novas aplicações da reação de Heck enantiosseletiva : dessimetrizações e reações intramoleculares: New applications of the enantioselective Heck reaction : desymmetrizations and intramolecular reactions.” 2018. Web. 06 Mar 2021.

Vancouver:

Carmona, Rafaela Costa 1. Novas aplicações da reação de Heck enantiosseletiva : dessimetrizações e reações intramoleculares: New applications of the enantioselective Heck reaction : desymmetrizations and intramolecular reactions. [Internet] [Thesis]. Universidade Estadual de Campinas; 2018. [cited 2021 Mar 06]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/331977.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Carmona, Rafaela Costa 1. Novas aplicações da reação de Heck enantiosseletiva : dessimetrizações e reações intramoleculares: New applications of the enantioselective Heck reaction : desymmetrizations and intramolecular reactions. [Thesis]. Universidade Estadual de Campinas; 2018. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/331977

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universidade Estadual de Campinas

18. Martinez, Pablo David Grigol, 1979-. Enecarbamatos endocíclicos como substratos na organocatálise : abordagens para a síntese de bases esfingóides e análogo da bulgecinina: Endocyclic enecarbamates as substrates in organocatalysis : approaches to sphingoid bases synthesis and bulgecinine analogue.

Degree: 2013, Universidade Estadual de Campinas

 Abstract: In the first part of this work, the use of endocyclic enecarbamates as substrates in organocatalysis was evaluated. The effect of phosphoric acids as… (more)

Subjects/Keywords: Enecarbamatos; Bases esfingoides; Heck-Matsuda, reação de; Hidrogenólise; Organocatálise; Enecarbamates; Sphingoid bases; Heck-Matsuda reaction; Hydrogenolysis; Organocatalysis

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APA (6th Edition):

Martinez, Pablo David Grigol, 1. (2013). Enecarbamatos endocíclicos como substratos na organocatálise : abordagens para a síntese de bases esfingóides e análogo da bulgecinina: Endocyclic enecarbamates as substrates in organocatalysis : approaches to sphingoid bases synthesis and bulgecinine analogue. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/249473

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Martinez, Pablo David Grigol, 1979-. “Enecarbamatos endocíclicos como substratos na organocatálise : abordagens para a síntese de bases esfingóides e análogo da bulgecinina: Endocyclic enecarbamates as substrates in organocatalysis : approaches to sphingoid bases synthesis and bulgecinine analogue.” 2013. Thesis, Universidade Estadual de Campinas. Accessed March 06, 2021. http://repositorio.unicamp.br/jspui/handle/REPOSIP/249473.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Martinez, Pablo David Grigol, 1979-. “Enecarbamatos endocíclicos como substratos na organocatálise : abordagens para a síntese de bases esfingóides e análogo da bulgecinina: Endocyclic enecarbamates as substrates in organocatalysis : approaches to sphingoid bases synthesis and bulgecinine analogue.” 2013. Web. 06 Mar 2021.

Vancouver:

Martinez, Pablo David Grigol 1. Enecarbamatos endocíclicos como substratos na organocatálise : abordagens para a síntese de bases esfingóides e análogo da bulgecinina: Endocyclic enecarbamates as substrates in organocatalysis : approaches to sphingoid bases synthesis and bulgecinine analogue. [Internet] [Thesis]. Universidade Estadual de Campinas; 2013. [cited 2021 Mar 06]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/249473.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Martinez, Pablo David Grigol 1. Enecarbamatos endocíclicos como substratos na organocatálise : abordagens para a síntese de bases esfingóides e análogo da bulgecinina: Endocyclic enecarbamates as substrates in organocatalysis : approaches to sphingoid bases synthesis and bulgecinine analogue. [Thesis]. Universidade Estadual de Campinas; 2013. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/249473

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

19. Dumonteil, Geoffrey. Synthèse et pharmacomodulations de composés naturels issus de plantes : Synthèse et pharmacomodulations de composés naturels issus de plantes.

Degree: Docteur es, Chimie, 2015, Université d'Orléans

Les motifs polyènes constituent une fonction importante parmi les composés organiques et sont présents dans de nombreux composés naturels sous la forme de diènes 1,3-conjugués.… (more)

Subjects/Keywords: Chimie verte; Produit naturel; Réaction de Heck; Catalyse à l’iode; Green chemistry; Natural product; Heck reaction; Iodine catalyst; 547

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Dumonteil, G. (2015). Synthèse et pharmacomodulations de composés naturels issus de plantes : Synthèse et pharmacomodulations de composés naturels issus de plantes. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2015ORLE2061

Chicago Manual of Style (16th Edition):

Dumonteil, Geoffrey. “Synthèse et pharmacomodulations de composés naturels issus de plantes : Synthèse et pharmacomodulations de composés naturels issus de plantes.” 2015. Doctoral Dissertation, Université d'Orléans. Accessed March 06, 2021. http://www.theses.fr/2015ORLE2061.

MLA Handbook (7th Edition):

Dumonteil, Geoffrey. “Synthèse et pharmacomodulations de composés naturels issus de plantes : Synthèse et pharmacomodulations de composés naturels issus de plantes.” 2015. Web. 06 Mar 2021.

Vancouver:

Dumonteil G. Synthèse et pharmacomodulations de composés naturels issus de plantes : Synthèse et pharmacomodulations de composés naturels issus de plantes. [Internet] [Doctoral dissertation]. Université d'Orléans; 2015. [cited 2021 Mar 06]. Available from: http://www.theses.fr/2015ORLE2061.

Council of Science Editors:

Dumonteil G. Synthèse et pharmacomodulations de composés naturels issus de plantes : Synthèse et pharmacomodulations de composés naturels issus de plantes. [Doctoral Dissertation]. Université d'Orléans; 2015. Available from: http://www.theses.fr/2015ORLE2061

20. Grüber, Raymond. Etude théorique de réactions de Heck intramoléculaires : Theoretical study of intramolecular Heck reactions.

Degree: Docteur es, Chimie, 2014, Lyon, École normale supérieure

L'ouverture de cycle aromatique catalysée par le palladium a été récemment observée par une équipe de l'ENSTA. Ce type de réactivité du palladium n’a jamais… (more)

Subjects/Keywords: Réaction de Heck; Ouverture furane; Benzofurane; Fonctionnelle; Catalyse; DFT; Mécanisme; Heck reaction; Furan opening; Benzofuran; Functional; Catalysis; DFT; Mechanism

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Grüber, R. (2014). Etude théorique de réactions de Heck intramoléculaires : Theoretical study of intramolecular Heck reactions. (Doctoral Dissertation). Lyon, École normale supérieure. Retrieved from http://www.theses.fr/2014ENSL0906

Chicago Manual of Style (16th Edition):

Grüber, Raymond. “Etude théorique de réactions de Heck intramoléculaires : Theoretical study of intramolecular Heck reactions.” 2014. Doctoral Dissertation, Lyon, École normale supérieure. Accessed March 06, 2021. http://www.theses.fr/2014ENSL0906.

MLA Handbook (7th Edition):

Grüber, Raymond. “Etude théorique de réactions de Heck intramoléculaires : Theoretical study of intramolecular Heck reactions.” 2014. Web. 06 Mar 2021.

Vancouver:

Grüber R. Etude théorique de réactions de Heck intramoléculaires : Theoretical study of intramolecular Heck reactions. [Internet] [Doctoral dissertation]. Lyon, École normale supérieure; 2014. [cited 2021 Mar 06]. Available from: http://www.theses.fr/2014ENSL0906.

Council of Science Editors:

Grüber R. Etude théorique de réactions de Heck intramoléculaires : Theoretical study of intramolecular Heck reactions. [Doctoral Dissertation]. Lyon, École normale supérieure; 2014. Available from: http://www.theses.fr/2014ENSL0906


Université Paris-Sud – Paris XI

21. Piou, Tiffany. Développement de nouvelles réactions domino impliquant une étape de fonctionnalisation C-H pour la synthèse d'hétérocycles : Development of new domino reactions involving C-H functionalization for the synthesis of heterocycles.

Degree: Docteur es, Chimie organique, 2012, Université Paris-Sud – Paris XI

Le projet scientifique a consisté au développement de nouveaux processus domino ayant pour étape clé la fonctionnalisation d’une liaison C-H. L’introduction de cette étape de… (more)

Subjects/Keywords: Réactions domino; Palladium; Oxindole; Activation C-H, Heck; Réaction Heck; Aminopalladation; Migration; Hétérocycle; Catalyse; Domino reactions; Palladium; Oxindole; C-H activation; Heck reaction; Aminopalladation; Migration; Heterocycles; Catalysis

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Piou, T. (2012). Développement de nouvelles réactions domino impliquant une étape de fonctionnalisation C-H pour la synthèse d'hétérocycles : Development of new domino reactions involving C-H functionalization for the synthesis of heterocycles. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2012PA112424

Chicago Manual of Style (16th Edition):

Piou, Tiffany. “Développement de nouvelles réactions domino impliquant une étape de fonctionnalisation C-H pour la synthèse d'hétérocycles : Development of new domino reactions involving C-H functionalization for the synthesis of heterocycles.” 2012. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed March 06, 2021. http://www.theses.fr/2012PA112424.

MLA Handbook (7th Edition):

Piou, Tiffany. “Développement de nouvelles réactions domino impliquant une étape de fonctionnalisation C-H pour la synthèse d'hétérocycles : Development of new domino reactions involving C-H functionalization for the synthesis of heterocycles.” 2012. Web. 06 Mar 2021.

Vancouver:

Piou T. Développement de nouvelles réactions domino impliquant une étape de fonctionnalisation C-H pour la synthèse d'hétérocycles : Development of new domino reactions involving C-H functionalization for the synthesis of heterocycles. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2012. [cited 2021 Mar 06]. Available from: http://www.theses.fr/2012PA112424.

Council of Science Editors:

Piou T. Développement de nouvelles réactions domino impliquant une étape de fonctionnalisation C-H pour la synthèse d'hétérocycles : Development of new domino reactions involving C-H functionalization for the synthesis of heterocycles. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2012. Available from: http://www.theses.fr/2012PA112424


Universidade Estadual de Campinas

22. Frota, Carlise, 1987-. Arilação de Heck-Matsuda em olefinas trissubstituídas : estudo metodológico e aplicação na síntese do meso-hexestrol: Heck-Matsuda arylation in trisubstituted olefins : methodological study and application in meso-hexestrol synthesis.

Degree: 2018, Universidade Estadual de Campinas

 Abstract: The present work had as general objective the methodological study of the Heck-Matsuda reaction in trisubstituted olefins and its synthetic application. In the first… (more)

Subjects/Keywords: Heck-Matsuda, reação de; Paládio; Reação regiosseletiva; Reação diastereosseletiva; Sais de diazônio; Heck-Matsuda reaction; Palladium; Regioselective reaction; Diastereoselective reaction; Diazonium salts

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Frota, Carlise, 1. (2018). Arilação de Heck-Matsuda em olefinas trissubstituídas : estudo metodológico e aplicação na síntese do meso-hexestrol: Heck-Matsuda arylation in trisubstituted olefins : methodological study and application in meso-hexestrol synthesis. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/331861

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Frota, Carlise, 1987-. “Arilação de Heck-Matsuda em olefinas trissubstituídas : estudo metodológico e aplicação na síntese do meso-hexestrol: Heck-Matsuda arylation in trisubstituted olefins : methodological study and application in meso-hexestrol synthesis.” 2018. Thesis, Universidade Estadual de Campinas. Accessed March 06, 2021. http://repositorio.unicamp.br/jspui/handle/REPOSIP/331861.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Frota, Carlise, 1987-. “Arilação de Heck-Matsuda em olefinas trissubstituídas : estudo metodológico e aplicação na síntese do meso-hexestrol: Heck-Matsuda arylation in trisubstituted olefins : methodological study and application in meso-hexestrol synthesis.” 2018. Web. 06 Mar 2021.

Vancouver:

Frota, Carlise 1. Arilação de Heck-Matsuda em olefinas trissubstituídas : estudo metodológico e aplicação na síntese do meso-hexestrol: Heck-Matsuda arylation in trisubstituted olefins : methodological study and application in meso-hexestrol synthesis. [Internet] [Thesis]. Universidade Estadual de Campinas; 2018. [cited 2021 Mar 06]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/331861.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Frota, Carlise 1. Arilação de Heck-Matsuda em olefinas trissubstituídas : estudo metodológico e aplicação na síntese do meso-hexestrol: Heck-Matsuda arylation in trisubstituted olefins : methodological study and application in meso-hexestrol synthesis. [Thesis]. Universidade Estadual de Campinas; 2018. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/331861

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université Paris-Sud – Paris XI

23. Alsalim, Rana. Contribution à la synthèse totale de la céphalotaxine : Contribution to the total synthesis of cephalotaxine.

Degree: Docteur es, Chimie organique, 2013, Université Paris-Sud – Paris XI

Depuis plus de 40 ans des chimistes se sont intéressés à l’extraction, à l’activité biologique et à la synthèse de l’homoharringtonine, un ester naturel de… (more)

Subjects/Keywords: Alcaloïdes; Céphalotaxine; Activité antileucémique; Synthèse totale; Réaction de Heck; Plan d’expérience; Réaction tandem Heck/oxa-Michael; Processus éco-compatible; Eau; Palladium; Hydro-arylation; Alkaloids; Cephalotaxine; Antileukemic activity; Total synthesis; Heck reaction; Experimental design; Tandem Heck/oxa-Michael reaction; Sustainable process; Water; Palladium; Hydro-arylation

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Alsalim, R. (2013). Contribution à la synthèse totale de la céphalotaxine : Contribution to the total synthesis of cephalotaxine. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2013PA114811

Chicago Manual of Style (16th Edition):

Alsalim, Rana. “Contribution à la synthèse totale de la céphalotaxine : Contribution to the total synthesis of cephalotaxine.” 2013. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed March 06, 2021. http://www.theses.fr/2013PA114811.

MLA Handbook (7th Edition):

Alsalim, Rana. “Contribution à la synthèse totale de la céphalotaxine : Contribution to the total synthesis of cephalotaxine.” 2013. Web. 06 Mar 2021.

Vancouver:

Alsalim R. Contribution à la synthèse totale de la céphalotaxine : Contribution to the total synthesis of cephalotaxine. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2013. [cited 2021 Mar 06]. Available from: http://www.theses.fr/2013PA114811.

Council of Science Editors:

Alsalim R. Contribution à la synthèse totale de la céphalotaxine : Contribution to the total synthesis of cephalotaxine. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2013. Available from: http://www.theses.fr/2013PA114811


Universidade Estadual de Campinas

24. Angnes, Ricardo Almir, 1991-. Reações enantiosseletivas de Heck em alcenos endocíclicos : uso de interações não covalentes atrativas na indução de diastereosseletividade: Enantioselective Heck reactions of endocyclic alkenes : use of attractive non-covalent interactions for the induction of diastereoselectivity.

Degree: 2019, Universidade Estadual de Campinas

 Abstract: The palladium catalyzed arylation of alkenes is an efficient strategy for the construction of carbon-carbon bonds. The enantioselectivity in these reactions can usually be… (more)

Subjects/Keywords: Heck-Matsuda, reação de; Catálise enantiosseletiva; Catalise por paládio; Interações não-covalentes; Reação diastereosseletiva; Heck-Matsuda reaction; Enantioselective catalysis; Palladium catalysts; Non-covalent interactions; Diastereoselective reaction

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APA (6th Edition):

Angnes, Ricardo Almir, 1. (2019). Reações enantiosseletivas de Heck em alcenos endocíclicos : uso de interações não covalentes atrativas na indução de diastereosseletividade: Enantioselective Heck reactions of endocyclic alkenes : use of attractive non-covalent interactions for the induction of diastereoselectivity. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/334705

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Angnes, Ricardo Almir, 1991-. “Reações enantiosseletivas de Heck em alcenos endocíclicos : uso de interações não covalentes atrativas na indução de diastereosseletividade: Enantioselective Heck reactions of endocyclic alkenes : use of attractive non-covalent interactions for the induction of diastereoselectivity.” 2019. Thesis, Universidade Estadual de Campinas. Accessed March 06, 2021. http://repositorio.unicamp.br/jspui/handle/REPOSIP/334705.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Angnes, Ricardo Almir, 1991-. “Reações enantiosseletivas de Heck em alcenos endocíclicos : uso de interações não covalentes atrativas na indução de diastereosseletividade: Enantioselective Heck reactions of endocyclic alkenes : use of attractive non-covalent interactions for the induction of diastereoselectivity.” 2019. Web. 06 Mar 2021.

Vancouver:

Angnes, Ricardo Almir 1. Reações enantiosseletivas de Heck em alcenos endocíclicos : uso de interações não covalentes atrativas na indução de diastereosseletividade: Enantioselective Heck reactions of endocyclic alkenes : use of attractive non-covalent interactions for the induction of diastereoselectivity. [Internet] [Thesis]. Universidade Estadual de Campinas; 2019. [cited 2021 Mar 06]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/334705.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Angnes, Ricardo Almir 1. Reações enantiosseletivas de Heck em alcenos endocíclicos : uso de interações não covalentes atrativas na indução de diastereosseletividade: Enantioselective Heck reactions of endocyclic alkenes : use of attractive non-covalent interactions for the induction of diastereoselectivity. [Thesis]. Universidade Estadual de Campinas; 2019. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/334705

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

25. Lacarriere, Tatiana. Etude synthétique d’un analogue azoté de la galanthamine. : Synthetic study of a galanthamine nitrogen analogue.

Degree: Docteur es, Chimie, 2015, Université Paris-Saclay (ComUE)

La synthèse de la 5-azagalanthamine, un analogue azoté de galanthamine, utilisée dans le traitement palliatif de la maladie d’Alzheimer, a été envisagée dans le cadre… (more)

Subjects/Keywords: 5-Azagalanthamine; Pictet-Spengler; Iode hypervalent; Couplage pallado-Catalysé; Heck intramoléculaire; 5-Azagalanthamine; Pictet-Spengler reaction; Hypervalent iodine; Palladium-Catalysed intramolecular coupling; Intramolecular Heck reaction

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APA (6th Edition):

Lacarriere, T. (2015). Etude synthétique d’un analogue azoté de la galanthamine. : Synthetic study of a galanthamine nitrogen analogue. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2015SACLS136

Chicago Manual of Style (16th Edition):

Lacarriere, Tatiana. “Etude synthétique d’un analogue azoté de la galanthamine. : Synthetic study of a galanthamine nitrogen analogue.” 2015. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed March 06, 2021. http://www.theses.fr/2015SACLS136.

MLA Handbook (7th Edition):

Lacarriere, Tatiana. “Etude synthétique d’un analogue azoté de la galanthamine. : Synthetic study of a galanthamine nitrogen analogue.” 2015. Web. 06 Mar 2021.

Vancouver:

Lacarriere T. Etude synthétique d’un analogue azoté de la galanthamine. : Synthetic study of a galanthamine nitrogen analogue. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2015. [cited 2021 Mar 06]. Available from: http://www.theses.fr/2015SACLS136.

Council of Science Editors:

Lacarriere T. Etude synthétique d’un analogue azoté de la galanthamine. : Synthetic study of a galanthamine nitrogen analogue. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2015. Available from: http://www.theses.fr/2015SACLS136


University of Alberta

26. Lee, Jack C. H. Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates.

Degree: PhD, Department of Chemistry, 2013, University of Alberta

 As Organic Chemistry evolves into the 21st Century, the goal of this discipline has altered dramatically from merely accessing target molecules to efficiently synthesizing these… (more)

Subjects/Keywords: Gold-catalyzed cycloisomerization; Suzuki-Miyaura cross-coupling; Chiral alkyl boronates; Heck reaction; Enantioselective conjugate addition

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APA (6th Edition):

Lee, J. C. H. (2013). Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/qn59q550n

Chicago Manual of Style (16th Edition):

Lee, Jack C H. “Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates.” 2013. Doctoral Dissertation, University of Alberta. Accessed March 06, 2021. https://era.library.ualberta.ca/files/qn59q550n.

MLA Handbook (7th Edition):

Lee, Jack C H. “Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates.” 2013. Web. 06 Mar 2021.

Vancouver:

Lee JCH. Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2021 Mar 06]. Available from: https://era.library.ualberta.ca/files/qn59q550n.

Council of Science Editors:

Lee JCH. Preparation and Synthetic Applications of Chiral Alkyl Boronates and Unsaturated Alkenyl Boronates. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/qn59q550n


Queens University

27. Cosman, Jennifer. Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions .

Degree: Chemistry, 2015, Queens University

 Chapter one of this thesis describes the iridium-catalyzed ortho-selective C–H borylation reaction of tertiary benzamides. An iridium(I) complex paired with an electron-deficient phosphine ligand allows… (more)

Subjects/Keywords: multicomponent reactions ; C-H activation ; allylic substitution ; Mizoroki-Heck reaction ; iridium-catalyzed C-H borylation

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APA (6th Edition):

Cosman, J. (2015). Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13534

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Cosman, Jennifer. “Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions .” 2015. Thesis, Queens University. Accessed March 06, 2021. http://hdl.handle.net/1974/13534.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Cosman, Jennifer. “Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions .” 2015. Web. 06 Mar 2021.

Vancouver:

Cosman J. Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions . [Internet] [Thesis]. Queens University; 2015. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1974/13534.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Cosman J. Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/13534

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Univerzitet u Beogradu

28. Tasić, Gordana D., 1973-. Ciklizacione reakcije alilnih alkohola katalizovane paladijumovim kompleksima.

Degree: Hemijski fakultet, 2016, Univerzitet u Beogradu

Hemija - Organska hemija / Chemistry - Organic Chemistry

Cilj ove doktorske disertacije bio je razvoj sintetičke metodologije za dobijanje funkcionalizovanih bicikličnih ketona čijom daljom… (more)

Subjects/Keywords: corialstonine; corialstonidine; bicyclo compounds; Heck reaction; regioselectivity; N-vinyl indole; isomerisation; debromoarborescidine B

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APA (6th Edition):

Tasić, Gordana D., 1. (2016). Ciklizacione reakcije alilnih alkohola katalizovane paladijumovim kompleksima. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:12428/bdef:Content/get

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Tasić, Gordana D., 1973-. “Ciklizacione reakcije alilnih alkohola katalizovane paladijumovim kompleksima.” 2016. Thesis, Univerzitet u Beogradu. Accessed March 06, 2021. https://fedorabg.bg.ac.rs/fedora/get/o:12428/bdef:Content/get.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Tasić, Gordana D., 1973-. “Ciklizacione reakcije alilnih alkohola katalizovane paladijumovim kompleksima.” 2016. Web. 06 Mar 2021.

Vancouver:

Tasić, Gordana D. 1. Ciklizacione reakcije alilnih alkohola katalizovane paladijumovim kompleksima. [Internet] [Thesis]. Univerzitet u Beogradu; 2016. [cited 2021 Mar 06]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:12428/bdef:Content/get.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Tasić, Gordana D. 1. Ciklizacione reakcije alilnih alkohola katalizovane paladijumovim kompleksima. [Thesis]. Univerzitet u Beogradu; 2016. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:12428/bdef:Content/get

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Kansas

29. Johnson, Thomas Seals. Synthesis and Applications of Amide-Based Pd(II) NNN-pincer Complexes.

Degree: MS, Chemistry, 2016, University of Kansas

 The first project is described in Chapter 2, and details the synthesis of a series of mono- and multimetallic Pd(II) NNN-pincer complexes which—to the best… (more)

Subjects/Keywords: Chemistry; Inorganic chemistry; Organic chemistry; Catalysis; Heck Reaction; Heterobimetallic; Macrocycle; Palladium; Pincer

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APA (6th Edition):

Johnson, T. S. (2016). Synthesis and Applications of Amide-Based Pd(II) NNN-pincer Complexes. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/21852

Chicago Manual of Style (16th Edition):

Johnson, Thomas Seals. “Synthesis and Applications of Amide-Based Pd(II) NNN-pincer Complexes.” 2016. Masters Thesis, University of Kansas. Accessed March 06, 2021. http://hdl.handle.net/1808/21852.

MLA Handbook (7th Edition):

Johnson, Thomas Seals. “Synthesis and Applications of Amide-Based Pd(II) NNN-pincer Complexes.” 2016. Web. 06 Mar 2021.

Vancouver:

Johnson TS. Synthesis and Applications of Amide-Based Pd(II) NNN-pincer Complexes. [Internet] [Masters thesis]. University of Kansas; 2016. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1808/21852.

Council of Science Editors:

Johnson TS. Synthesis and Applications of Amide-Based Pd(II) NNN-pincer Complexes. [Masters Thesis]. University of Kansas; 2016. Available from: http://hdl.handle.net/1808/21852


Univerzitet u Beogradu

30. Bigović, Miljan R. 1984-. Alilovanje visoko-funkcionalizovanim organometalnim reagensima: 4-(brommetil)-1,3-dioksol-2-on kao sintetički ekvivalent enolata hidroksiketona.

Degree: Hemijski fakultet, 2016, Univerzitet u Beogradu

Prirodno-matematičke nauke - Organska hemija / Life sciences - Organic chemistry

Razvijen je novi metod alilovanja karbonilnih jedinjenja pomoću 4-(brommetil)-1,3- dioksol-2-ona, kao visoko funkcionalizovanog alilujućeg… (more)

Subjects/Keywords: allylation / indium / zinc / Barbier reaction / Heck reaction / enol carbonates / α; β-dihydroxyketones / cyclic carbonates / deprotection / isomerization

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APA (6th Edition):

Bigović, M. R. 1. (2016). Alilovanje visoko-funkcionalizovanim organometalnim reagensima: 4-(brommetil)-1,3-dioksol-2-on kao sintetički ekvivalent enolata hidroksiketona. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:11601/bdef:Content/get

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Bigović, Miljan R 1984-. “Alilovanje visoko-funkcionalizovanim organometalnim reagensima: 4-(brommetil)-1,3-dioksol-2-on kao sintetički ekvivalent enolata hidroksiketona.” 2016. Thesis, Univerzitet u Beogradu. Accessed March 06, 2021. https://fedorabg.bg.ac.rs/fedora/get/o:11601/bdef:Content/get.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Bigović, Miljan R 1984-. “Alilovanje visoko-funkcionalizovanim organometalnim reagensima: 4-(brommetil)-1,3-dioksol-2-on kao sintetički ekvivalent enolata hidroksiketona.” 2016. Web. 06 Mar 2021.

Vancouver:

Bigović MR1. Alilovanje visoko-funkcionalizovanim organometalnim reagensima: 4-(brommetil)-1,3-dioksol-2-on kao sintetički ekvivalent enolata hidroksiketona. [Internet] [Thesis]. Univerzitet u Beogradu; 2016. [cited 2021 Mar 06]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:11601/bdef:Content/get.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Bigović MR1. Alilovanje visoko-funkcionalizovanim organometalnim reagensima: 4-(brommetil)-1,3-dioksol-2-on kao sintetički ekvivalent enolata hidroksiketona. [Thesis]. Univerzitet u Beogradu; 2016. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:11601/bdef:Content/get

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

[1] [2] [3]

.