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You searched for subject:(Suzuki reaction). Showing records 1 – 30 of 58 total matches.

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University of Saskatchewan

1. Li, Hanxiang 1989-. The versatility of palladium systems: from palladacycles to cyclic peptides and beyond.

Degree: 2015, University of Saskatchewan

 This work started with the aim to synthesize monomeric ring-opened analogues of the palladacycles [(iminoisoidoline)PdCl(PCy3)] incorporating iminoisoindoline and phosphine ligands, and evaluate their catalytic activities… (more)

Subjects/Keywords: palladacycle; cyclic peptide; suzuki reaction

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APA (6th Edition):

Li, H. 1. (2015). The versatility of palladium systems: from palladacycles to cyclic peptides and beyond. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12420

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):

Li, Hanxiang 1989-. “The versatility of palladium systems: from palladacycles to cyclic peptides and beyond.” 2015. Thesis, University of Saskatchewan. Accessed March 07, 2021. http://hdl.handle.net/10388/12420.

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

MLA Handbook (7th Edition):

Li, Hanxiang 1989-. “The versatility of palladium systems: from palladacycles to cyclic peptides and beyond.” 2015. Web. 07 Mar 2021.

Vancouver:

Li H1. The versatility of palladium systems: from palladacycles to cyclic peptides and beyond. [Internet] [Thesis]. University of Saskatchewan; 2015. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/10388/12420.

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

Council of Science Editors:

Li H1. The versatility of palladium systems: from palladacycles to cyclic peptides and beyond. [Thesis]. University of Saskatchewan; 2015. Available from: http://hdl.handle.net/10388/12420

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


Johannes Gutenberg Universität Mainz

2. Breuch, Denis. Kontinuierliche Kreuzkupplungsreaktionen in mikrostrukturierten Systemen.

Degree: 2013, Johannes Gutenberg Universität Mainz

Im Rahmen dieser Arbeit wurden unterschiedliche Palladium-katalysierte Kreuzkupplungsreaktionen untersucht. Ein besonderes Augenmerk wurde dabei auf die Suzuki-Miyaura-Reaktion gelegt. Unter anderem aufgrund der langen Reaktionszeiten und… (more)

Subjects/Keywords: Mikroreaktor; Suzuki-Reaktion; ionische Flüssigkeit; micro reactor; Suzuki reaction; ionic liquid; Chemistry and allied sciences

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APA (6th Edition):

Breuch, D. (2013). Kontinuierliche Kreuzkupplungsreaktionen in mikrostrukturierten Systemen. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2013/3443/

Chicago Manual of Style (16th Edition):

Breuch, Denis. “Kontinuierliche Kreuzkupplungsreaktionen in mikrostrukturierten Systemen.” 2013. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed March 07, 2021. http://ubm.opus.hbz-nrw.de/volltexte/2013/3443/.

MLA Handbook (7th Edition):

Breuch, Denis. “Kontinuierliche Kreuzkupplungsreaktionen in mikrostrukturierten Systemen.” 2013. Web. 07 Mar 2021.

Vancouver:

Breuch D. Kontinuierliche Kreuzkupplungsreaktionen in mikrostrukturierten Systemen. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2013. [cited 2021 Mar 07]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3443/.

Council of Science Editors:

Breuch D. Kontinuierliche Kreuzkupplungsreaktionen in mikrostrukturierten Systemen. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2013. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3443/

3. Takimoto, Herick Garcia. Estudo de polifluorenos como camada emissora de dispositivos eletroluminescentes eficientes.

Degree: Mestrado, Engenharia Metalúrgica e de Materiais, 2013, University of São Paulo

Este trabalho tem como principais objetivos: desenvolver procedimentos sintéticos e novos materiais poliméricos que apresentem boa condutividade elétrica, estudar o comportamento eletro-óptico dos polímeros obtidos,… (more)

Subjects/Keywords: ITO; ITO; P-OLEDs; P-OLEDs; Polifluoreno; Polyfluorene; Reação Suzuki; Suzuki reaction

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APA (6th Edition):

Takimoto, H. G. (2013). Estudo de polifluorenos como camada emissora de dispositivos eletroluminescentes eficientes. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/3/3133/tde-23052014-014442/ ;

Chicago Manual of Style (16th Edition):

Takimoto, Herick Garcia. “Estudo de polifluorenos como camada emissora de dispositivos eletroluminescentes eficientes.” 2013. Masters Thesis, University of São Paulo. Accessed March 07, 2021. http://www.teses.usp.br/teses/disponiveis/3/3133/tde-23052014-014442/ ;.

MLA Handbook (7th Edition):

Takimoto, Herick Garcia. “Estudo de polifluorenos como camada emissora de dispositivos eletroluminescentes eficientes.” 2013. Web. 07 Mar 2021.

Vancouver:

Takimoto HG. Estudo de polifluorenos como camada emissora de dispositivos eletroluminescentes eficientes. [Internet] [Masters thesis]. University of São Paulo; 2013. [cited 2021 Mar 07]. Available from: http://www.teses.usp.br/teses/disponiveis/3/3133/tde-23052014-014442/ ;.

Council of Science Editors:

Takimoto HG. Estudo de polifluorenos como camada emissora de dispositivos eletroluminescentes eficientes. [Masters Thesis]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/3/3133/tde-23052014-014442/ ;


University of KwaZulu-Natal

4. Molefe, Patience Snenhlanhla Sthembile. Base-Free Suzuki acylation reactions of sodium (aryl trihydroxyborate) salts: a novel synthesis of substituted aryl ketones.

Degree: 2018, University of KwaZulu-Natal

 Asymmetric biaryl ketones are important building block in organic chemistry since they occur in large number of biological active compounds, natural product, cosmetics as well… (more)

Subjects/Keywords: Base-free Suzuki.; Sodium salts.; Aryl trihydroxyborate.; Ketones.; Suzuki-Miyaura cross-coupling acylation reaction.

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APA (6th Edition):

Molefe, P. S. S. (2018). Base-Free Suzuki acylation reactions of sodium (aryl trihydroxyborate) salts: a novel synthesis of substituted aryl ketones. (Thesis). University of KwaZulu-Natal. Retrieved from https://researchspace.ukzn.ac.za/handle/10413/18146

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):

Molefe, Patience Snenhlanhla Sthembile. “Base-Free Suzuki acylation reactions of sodium (aryl trihydroxyborate) salts: a novel synthesis of substituted aryl ketones.” 2018. Thesis, University of KwaZulu-Natal. Accessed March 07, 2021. https://researchspace.ukzn.ac.za/handle/10413/18146.

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

MLA Handbook (7th Edition):

Molefe, Patience Snenhlanhla Sthembile. “Base-Free Suzuki acylation reactions of sodium (aryl trihydroxyborate) salts: a novel synthesis of substituted aryl ketones.” 2018. Web. 07 Mar 2021.

Vancouver:

Molefe PSS. Base-Free Suzuki acylation reactions of sodium (aryl trihydroxyborate) salts: a novel synthesis of substituted aryl ketones. [Internet] [Thesis]. University of KwaZulu-Natal; 2018. [cited 2021 Mar 07]. Available from: https://researchspace.ukzn.ac.za/handle/10413/18146.

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

Council of Science Editors:

Molefe PSS. Base-Free Suzuki acylation reactions of sodium (aryl trihydroxyborate) salts: a novel synthesis of substituted aryl ketones. [Thesis]. University of KwaZulu-Natal; 2018. Available from: https://researchspace.ukzn.ac.za/handle/10413/18146

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


Virginia Commonwealth University

5. Martin, Alex D. A Convergent Approach to the Continuous Synthesis of Telmisartan via a Suzuki Reaction between Two Functionalized Benzimidazoles.

Degree: PhD, Chemistry, 2015, Virginia Commonwealth University

  A direct and highly efficient synthesis has been developed for telmisartan, the active ingredient in the widely prescribed antihypertensive drug Micardis®. This approach brings… (more)

Subjects/Keywords: telmisartan; suzuki reaction; flow chemistry; API synthesis; antihypertensive; Organic Chemistry

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APA (6th Edition):

Martin, A. D. (2015). A Convergent Approach to the Continuous Synthesis of Telmisartan via a Suzuki Reaction between Two Functionalized Benzimidazoles. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/2TDP-NQ30 ; https://scholarscompass.vcu.edu/etd/3750

Chicago Manual of Style (16th Edition):

Martin, Alex D. “A Convergent Approach to the Continuous Synthesis of Telmisartan via a Suzuki Reaction between Two Functionalized Benzimidazoles.” 2015. Doctoral Dissertation, Virginia Commonwealth University. Accessed March 07, 2021. https://doi.org/10.25772/2TDP-NQ30 ; https://scholarscompass.vcu.edu/etd/3750.

MLA Handbook (7th Edition):

Martin, Alex D. “A Convergent Approach to the Continuous Synthesis of Telmisartan via a Suzuki Reaction between Two Functionalized Benzimidazoles.” 2015. Web. 07 Mar 2021.

Vancouver:

Martin AD. A Convergent Approach to the Continuous Synthesis of Telmisartan via a Suzuki Reaction between Two Functionalized Benzimidazoles. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2015. [cited 2021 Mar 07]. Available from: https://doi.org/10.25772/2TDP-NQ30 ; https://scholarscompass.vcu.edu/etd/3750.

Council of Science Editors:

Martin AD. A Convergent Approach to the Continuous Synthesis of Telmisartan via a Suzuki Reaction between Two Functionalized Benzimidazoles. [Doctoral Dissertation]. Virginia Commonwealth University; 2015. Available from: https://doi.org/10.25772/2TDP-NQ30 ; https://scholarscompass.vcu.edu/etd/3750


Boston College

6. Eliseeva, Maria N. New Route to a [5,5] Carbon Nanotube End-Cap via Direct Borylation of Corannulene.

Degree: MS, Chemistry, 2011, Boston College

 The Scott lab is interested in the functionalization of corannulene as a building block for large polycyclic aromatic hydrocarbons and carbon nanotube end-cap precursors. Toward… (more)

Subjects/Keywords: carbon nanotube; corannulene; direct borylation; iridium catalyst; Suzuki reaction

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APA (6th Edition):

Eliseeva, M. N. (2011). New Route to a [5,5] Carbon Nanotube End-Cap via Direct Borylation of Corannulene. (Masters Thesis). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101796

Chicago Manual of Style (16th Edition):

Eliseeva, Maria N. “New Route to a [5,5] Carbon Nanotube End-Cap via Direct Borylation of Corannulene.” 2011. Masters Thesis, Boston College. Accessed March 07, 2021. http://dlib.bc.edu/islandora/object/bc-ir:101796.

MLA Handbook (7th Edition):

Eliseeva, Maria N. “New Route to a [5,5] Carbon Nanotube End-Cap via Direct Borylation of Corannulene.” 2011. Web. 07 Mar 2021.

Vancouver:

Eliseeva MN. New Route to a [5,5] Carbon Nanotube End-Cap via Direct Borylation of Corannulene. [Internet] [Masters thesis]. Boston College; 2011. [cited 2021 Mar 07]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101796.

Council of Science Editors:

Eliseeva MN. New Route to a [5,5] Carbon Nanotube End-Cap via Direct Borylation of Corannulene. [Masters Thesis]. Boston College; 2011. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101796


University of South Carolina

7. Key, Ryan J. Development of Nickel Catalyzed Cross-Coupling Methodologies.

Degree: PhD, Chemistry and Biochemistry, 2019, University of South Carolina

  In this work, we have addressed some of the issues surrounding catalytic crosscoupling reactions by using a nickel terpyridine catalyst, [Ni(tpy)(py)(CH3CN)2](PF6)2 in the Buchwald-Hartwig… (more)

Subjects/Keywords: Chemistry; nickel; cross-coupling; Atomic Layer Deposition; Suzuki reaction

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APA (6th Edition):

Key, R. J. (2019). Development of Nickel Catalyzed Cross-Coupling Methodologies. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/5324

Chicago Manual of Style (16th Edition):

Key, Ryan J. “Development of Nickel Catalyzed Cross-Coupling Methodologies.” 2019. Doctoral Dissertation, University of South Carolina. Accessed March 07, 2021. https://scholarcommons.sc.edu/etd/5324.

MLA Handbook (7th Edition):

Key, Ryan J. “Development of Nickel Catalyzed Cross-Coupling Methodologies.” 2019. Web. 07 Mar 2021.

Vancouver:

Key RJ. Development of Nickel Catalyzed Cross-Coupling Methodologies. [Internet] [Doctoral dissertation]. University of South Carolina; 2019. [cited 2021 Mar 07]. Available from: https://scholarcommons.sc.edu/etd/5324.

Council of Science Editors:

Key RJ. Development of Nickel Catalyzed Cross-Coupling Methodologies. [Doctoral Dissertation]. University of South Carolina; 2019. Available from: https://scholarcommons.sc.edu/etd/5324

8. Geogheghan, Katherine Jayne. Boronic acid speciation in Suzuki-Miyaura cross-coupling.

Degree: PhD, 2018, University of Edinburgh

 Since its discovery in 1979, the Suzuki-Miyaura (SM) reaction has become one of the most widely utilised tools for carbon-carbon bond formation. The palladium catalysed… (more)

Subjects/Keywords: 660; cross-coupling; Suzuki-Miyaura reaction; palladium catalysed coupling; boronic esters

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APA (6th Edition):

Geogheghan, K. J. (2018). Boronic acid speciation in Suzuki-Miyaura cross-coupling. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/33092

Chicago Manual of Style (16th Edition):

Geogheghan, Katherine Jayne. “Boronic acid speciation in Suzuki-Miyaura cross-coupling.” 2018. Doctoral Dissertation, University of Edinburgh. Accessed March 07, 2021. http://hdl.handle.net/1842/33092.

MLA Handbook (7th Edition):

Geogheghan, Katherine Jayne. “Boronic acid speciation in Suzuki-Miyaura cross-coupling.” 2018. Web. 07 Mar 2021.

Vancouver:

Geogheghan KJ. Boronic acid speciation in Suzuki-Miyaura cross-coupling. [Internet] [Doctoral dissertation]. University of Edinburgh; 2018. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1842/33092.

Council of Science Editors:

Geogheghan KJ. Boronic acid speciation in Suzuki-Miyaura cross-coupling. [Doctoral Dissertation]. University of Edinburgh; 2018. Available from: http://hdl.handle.net/1842/33092


Universidade Federal de Viçosa

9. Guilherme Carvalho Geraldo. Síntese e avaliação da atividade fitotóxica de análogos ao alternariol.

Degree: 2008, Universidade Federal de Viçosa

O alternariol é uma lactona aromática produzida por espécies fúngicas fitopatogênicas dos gêneros Nimbya e Alternaria. Estas espécies são conhecidas por causarem necroses foliares ocasionando… (more)

Subjects/Keywords: Alternariol; Herbicidas; Fungos fitopatogênicos; Acoplamento de Suzuki; QUIMICA ORGANICA; Alternariol; Herbicides; Plant pathogenic fungi; Suzuki coupling reaction

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APA (6th Edition):

Geraldo, G. C. (2008). Síntese e avaliação da atividade fitotóxica de análogos ao alternariol. (Thesis). Universidade Federal de Viçosa. Retrieved from http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=1891

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):

Geraldo, Guilherme Carvalho. “Síntese e avaliação da atividade fitotóxica de análogos ao alternariol.” 2008. Thesis, Universidade Federal de Viçosa. Accessed March 07, 2021. http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=1891.

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

MLA Handbook (7th Edition):

Geraldo, Guilherme Carvalho. “Síntese e avaliação da atividade fitotóxica de análogos ao alternariol.” 2008. Web. 07 Mar 2021.

Vancouver:

Geraldo GC. Síntese e avaliação da atividade fitotóxica de análogos ao alternariol. [Internet] [Thesis]. Universidade Federal de Viçosa; 2008. [cited 2021 Mar 07]. Available from: http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=1891.

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

Council of Science Editors:

Geraldo GC. Síntese e avaliação da atividade fitotóxica de análogos ao alternariol. [Thesis]. Universidade Federal de Viçosa; 2008. Available from: http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=1891

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


Vilnius University

10. Dodonova, Jelena. Pirolo[2,3-d]pirimidino oligoarilenų sintezė ir fotofizikinės savybės.

Degree: PhD, Chemistry, 2012, Vilnius University

Šio darbo tikslas buvo susintetinti pirolo[2,3-d]pirimidino oligoarilenus ir ištirti jų fotofizikines savybes. Rezultate, ištirta 2,4-dichlorpirolo[2,3-d]pirimidino Suzuki reakcija su arilborono rūgštimis bei susintetinti nauji 4-aril- ir… (more)

Subjects/Keywords: Pirolo[2; 3-d]pirimidinas; Fluorescencija; Suzuki reakcija; N-arilinimas; Pyrrolo[2; 3-d]pyrimidine; Fluorescence; Suzuki reaction; N-arylation

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APA (6th Edition):

Dodonova, J. (2012). Pirolo[2,3-d]pirimidino oligoarilenų sintezė ir fotofizikinės savybės. (Doctoral Dissertation). Vilnius University. Retrieved from http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2012~D_20120917_092617-49864 ;

Chicago Manual of Style (16th Edition):

Dodonova, Jelena. “Pirolo[2,3-d]pirimidino oligoarilenų sintezė ir fotofizikinės savybės.” 2012. Doctoral Dissertation, Vilnius University. Accessed March 07, 2021. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2012~D_20120917_092617-49864 ;.

MLA Handbook (7th Edition):

Dodonova, Jelena. “Pirolo[2,3-d]pirimidino oligoarilenų sintezė ir fotofizikinės savybės.” 2012. Web. 07 Mar 2021.

Vancouver:

Dodonova J. Pirolo[2,3-d]pirimidino oligoarilenų sintezė ir fotofizikinės savybės. [Internet] [Doctoral dissertation]. Vilnius University; 2012. [cited 2021 Mar 07]. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2012~D_20120917_092617-49864 ;.

Council of Science Editors:

Dodonova J. Pirolo[2,3-d]pirimidino oligoarilenų sintezė ir fotofizikinės savybės. [Doctoral Dissertation]. Vilnius University; 2012. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2012~D_20120917_092617-49864 ;


Vilnius University

11. Dodonova, Jelena. Synthesis and photophysical properties of pyrrolo[2,3-d]pyrimidine-core based oligoarylenes.

Degree: Dissertation, Chemistry, 2012, Vilnius University

The main goal of the present work was to synthesize pyrrolo[2,3-d]pyrimidine core based oligoarylenes and to evaluate their photophysical properties. As a result, the Suzuki(more)

Subjects/Keywords: Pyrrolo[2; 3-d]pyrimidine; Fluorescence; Suzuki reaction; N-arylation; Pirolo[2; 3-d]pirimidinas; Fluorescencija; Suzuki reakcija; N-arilinimas

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APA (6th Edition):

Dodonova, J. (2012). Synthesis and photophysical properties of pyrrolo[2,3-d]pyrimidine-core based oligoarylenes. (Doctoral Dissertation). Vilnius University. Retrieved from http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2012~D_20120917_092627-68184 ;

Chicago Manual of Style (16th Edition):

Dodonova, Jelena. “Synthesis and photophysical properties of pyrrolo[2,3-d]pyrimidine-core based oligoarylenes.” 2012. Doctoral Dissertation, Vilnius University. Accessed March 07, 2021. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2012~D_20120917_092627-68184 ;.

MLA Handbook (7th Edition):

Dodonova, Jelena. “Synthesis and photophysical properties of pyrrolo[2,3-d]pyrimidine-core based oligoarylenes.” 2012. Web. 07 Mar 2021.

Vancouver:

Dodonova J. Synthesis and photophysical properties of pyrrolo[2,3-d]pyrimidine-core based oligoarylenes. [Internet] [Doctoral dissertation]. Vilnius University; 2012. [cited 2021 Mar 07]. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2012~D_20120917_092627-68184 ;.

Council of Science Editors:

Dodonova J. Synthesis and photophysical properties of pyrrolo[2,3-d]pyrimidine-core based oligoarylenes. [Doctoral Dissertation]. Vilnius University; 2012. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2012~D_20120917_092627-68184 ;

12. François, Benjamin. Utilisation d’organoboranes fonctionnalisés pour la construction de structures polycycliques : Functionalized organoboron compounds for the synthesis of polycyclic scaffolds.

Degree: Docteur es, Chimie moléculaire et macromoléculaire, 2018, Rennes 1

Les composés organoborés constituent des outils remarquables en synthèse organique de par leur chimie très diversifiée. Les travaux présentés dans ce mémoire abordent de nouveaux… (more)

Subjects/Keywords: Synthèse; Cascade; Organoboranes; Couplage de Suzuki; Réaction ène; Pyrrole; Synthesis; Cascade; Organoboranes; Suzuki coupling; Ene reaction; Pyrrole

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APA (6th Edition):

François, B. (2018). Utilisation d’organoboranes fonctionnalisés pour la construction de structures polycycliques : Functionalized organoboron compounds for the synthesis of polycyclic scaffolds. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2018REN1S114

Chicago Manual of Style (16th Edition):

François, Benjamin. “Utilisation d’organoboranes fonctionnalisés pour la construction de structures polycycliques : Functionalized organoboron compounds for the synthesis of polycyclic scaffolds.” 2018. Doctoral Dissertation, Rennes 1. Accessed March 07, 2021. http://www.theses.fr/2018REN1S114.

MLA Handbook (7th Edition):

François, Benjamin. “Utilisation d’organoboranes fonctionnalisés pour la construction de structures polycycliques : Functionalized organoboron compounds for the synthesis of polycyclic scaffolds.” 2018. Web. 07 Mar 2021.

Vancouver:

François B. Utilisation d’organoboranes fonctionnalisés pour la construction de structures polycycliques : Functionalized organoboron compounds for the synthesis of polycyclic scaffolds. [Internet] [Doctoral dissertation]. Rennes 1; 2018. [cited 2021 Mar 07]. Available from: http://www.theses.fr/2018REN1S114.

Council of Science Editors:

François B. Utilisation d’organoboranes fonctionnalisés pour la construction de structures polycycliques : Functionalized organoboron compounds for the synthesis of polycyclic scaffolds. [Doctoral Dissertation]. Rennes 1; 2018. Available from: http://www.theses.fr/2018REN1S114

13. Fodor, Anna. Heterogeneous metal-catalysed C-C coupling reactions : research and development : Réactions de couplage C-C réalisée par catalyse hétérogène : recherche et développement.

Degree: Docteur es, Chimie organique, minérale, industrielle, 2016, Poitiers; Budapesti Műszaki és Gazdaságtudományi Egyetem (Budapest)

Des nouveaux catalyseurs bimétalliques à base de palladium et de cuivre ont été développés. Deux voies de préparation ont été testées : l'imprégnation successive (TSI)… (more)

Subjects/Keywords: Catalyse bimétallique; Alliage cuivre-Palladium; Réaction de Suzuki; Réaction de Petasis; Effet du support; Bimetallic catalysis; Copper-Palladium alloy; Suzuki reaction; Petasis reaction; Effect of the support; 541.395

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

APA (6th Edition):

Fodor, A. (2016). Heterogeneous metal-catalysed C-C coupling reactions : research and development : Réactions de couplage C-C réalisée par catalyse hétérogène : recherche et développement. (Doctoral Dissertation). Poitiers; Budapesti Műszaki és Gazdaságtudományi Egyetem (Budapest). Retrieved from http://www.theses.fr/2016POIT2256

Chicago Manual of Style (16th Edition):

Fodor, Anna. “Heterogeneous metal-catalysed C-C coupling reactions : research and development : Réactions de couplage C-C réalisée par catalyse hétérogène : recherche et développement.” 2016. Doctoral Dissertation, Poitiers; Budapesti Műszaki és Gazdaságtudományi Egyetem (Budapest). Accessed March 07, 2021. http://www.theses.fr/2016POIT2256.

MLA Handbook (7th Edition):

Fodor, Anna. “Heterogeneous metal-catalysed C-C coupling reactions : research and development : Réactions de couplage C-C réalisée par catalyse hétérogène : recherche et développement.” 2016. Web. 07 Mar 2021.

Vancouver:

Fodor A. Heterogeneous metal-catalysed C-C coupling reactions : research and development : Réactions de couplage C-C réalisée par catalyse hétérogène : recherche et développement. [Internet] [Doctoral dissertation]. Poitiers; Budapesti Műszaki és Gazdaságtudományi Egyetem (Budapest); 2016. [cited 2021 Mar 07]. Available from: http://www.theses.fr/2016POIT2256.

Council of Science Editors:

Fodor A. Heterogeneous metal-catalysed C-C coupling reactions : research and development : Réactions de couplage C-C réalisée par catalyse hétérogène : recherche et développement. [Doctoral Dissertation]. Poitiers; Budapesti Műszaki és Gazdaságtudományi Egyetem (Budapest); 2016. Available from: http://www.theses.fr/2016POIT2256


NSYSU

14. Huang, Hao-ping. Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling.

Degree: Master, Chemistry, 2013, NSYSU

 The direct ortho arylation of 4-methyl-N-phenylpyridin-2-amines via palladium(II)-catalyzed C-H activation is described. Treatment of 4-methyl-N-phenylpyridin-2-amine with potassium aryltrifluoroborate using ten mol % of Pd(OAc)2 as… (more)

Subjects/Keywords: palladium; C-H bond activation; potassium aryltrifluoroborate; Suzuki-Miyaura cross-coupling reaction

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APA (6th Edition):

Huang, H. (2013). Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051

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):

Huang, Hao-ping. “Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling.” 2013. Thesis, NSYSU. Accessed March 07, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051.

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

MLA Handbook (7th Edition):

Huang, Hao-ping. “Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling.” 2013. Web. 07 Mar 2021.

Vancouver:

Huang H. Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling. [Internet] [Thesis]. NSYSU; 2013. [cited 2021 Mar 07]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051.

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

Council of Science Editors:

Huang H. Palladium(II)-Catalyzed Direct Ortho Arylation of 4-Methyl-N-phenylpyridin-2-amines via Suzuki-Miyaura Type C-H Bond Activation/C-C Bond Coupling. [Thesis]. NSYSU; 2013. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0406113-201051

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


NSYSU

15. Wu, Chung-chiu. Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation.

Degree: Master, Chemistry, 2012, NSYSU

 A one-pot synthesis of ortho-arylated 9-(pyridin-2-yl)-9H-carbazoles via C-H bond activation, in which palladium(II)-catalyzed cross-coupling of 9-(pyridin-2-yl)-9H-carbazoles with potassium aryltrifluoroborates is presented. Silver nitrate and tert-butanol… (more)

Subjects/Keywords: potassium aryltrifluoroborate; palladium catalysis; C-H bond activation; carbazole; Suzuki-Miyaura coupling reaction

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APA (6th Edition):

Wu, C. (2012). Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0709112-170941

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):

Wu, Chung-chiu. “Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation.” 2012. Thesis, NSYSU. Accessed March 07, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0709112-170941.

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

MLA Handbook (7th Edition):

Wu, Chung-chiu. “Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation.” 2012. Web. 07 Mar 2021.

Vancouver:

Wu C. Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation. [Internet] [Thesis]. NSYSU; 2012. [cited 2021 Mar 07]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0709112-170941.

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

Council of Science Editors:

Wu C. Palladium (II)-Catalyzed Ortho Arylation of 9-(Pyridin-2-yl)-9H-carbazoles via C-H Bond Activation And Mechanistic Investigation. [Thesis]. NSYSU; 2012. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0709112-170941

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


University of Alberta

16. 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 07, 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. 07 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 07]. 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


Virginia Commonwealth University

17. Yang, Yuan. Graphene as a Solid-state Ligand for Palladium Catalyzed Cross-coupling Reactions.

Degree: PhD, Engineering, 2018, Virginia Commonwealth University

  Palladium-catalyzed carbon-carbon cross-coupling reactions have emerged a broadly useful, selective and widely applicable method to synthesize pharmaceutical active ingredients. As currently practiced in the… (more)

Subjects/Keywords: Graphene Nanocatalysis heterogeneous Suzuki Palladium; Catalysis and Reaction Engineering; Nanoscience and Nanotechnology

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APA (6th Edition):

Yang, Y. (2018). Graphene as a Solid-state Ligand for Palladium Catalyzed Cross-coupling Reactions. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/562K-7355 ; https://scholarscompass.vcu.edu/etd/5488

Chicago Manual of Style (16th Edition):

Yang, Yuan. “Graphene as a Solid-state Ligand for Palladium Catalyzed Cross-coupling Reactions.” 2018. Doctoral Dissertation, Virginia Commonwealth University. Accessed March 07, 2021. https://doi.org/10.25772/562K-7355 ; https://scholarscompass.vcu.edu/etd/5488.

MLA Handbook (7th Edition):

Yang, Yuan. “Graphene as a Solid-state Ligand for Palladium Catalyzed Cross-coupling Reactions.” 2018. Web. 07 Mar 2021.

Vancouver:

Yang Y. Graphene as a Solid-state Ligand for Palladium Catalyzed Cross-coupling Reactions. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2018. [cited 2021 Mar 07]. Available from: https://doi.org/10.25772/562K-7355 ; https://scholarscompass.vcu.edu/etd/5488.

Council of Science Editors:

Yang Y. Graphene as a Solid-state Ligand for Palladium Catalyzed Cross-coupling Reactions. [Doctoral Dissertation]. Virginia Commonwealth University; 2018. Available from: https://doi.org/10.25772/562K-7355 ; https://scholarscompass.vcu.edu/etd/5488


Univerzitet u Beogradu

18. Aleksić, Jovana. 1980-. 4-oksotiazolidin-2-alkiliden vinil-bromidi i α, α-dibrom-2-metoksiacetofenon : prekursori u sintetički korisnim transformacijama iniciranim retkim halofilnim napadom nukleofila.

Degree: Hemijski fakultet, 2014, Univerzitet u Beogradu

Hemija - Organska hemija / Chemistry - Organic chemistry Datum odbrane: 8.03.2013.

Halofilne reakcije predstavljaju vrstu nukleofilnih supstitucionih reakcija do kojih dolazi kada nukleofil reaguje… (more)

Subjects/Keywords: halophilic reactions; vinyl halides; ; -dibromoacetophenones; Suzuki- Miyaura reaction; push-pull effect; NBO analysis

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APA (6th Edition):

Aleksić, J. 1. (2014). 4-oksotiazolidin-2-alkiliden vinil-bromidi i α, α-dibrom-2-metoksiacetofenon : prekursori u sintetički korisnim transformacijama iniciranim retkim halofilnim napadom nukleofila. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:8119/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):

Aleksić, Jovana 1980-. “4-oksotiazolidin-2-alkiliden vinil-bromidi i α, α-dibrom-2-metoksiacetofenon : prekursori u sintetički korisnim transformacijama iniciranim retkim halofilnim napadom nukleofila.” 2014. Thesis, Univerzitet u Beogradu. Accessed March 07, 2021. https://fedorabg.bg.ac.rs/fedora/get/o:8119/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):

Aleksić, Jovana 1980-. “4-oksotiazolidin-2-alkiliden vinil-bromidi i α, α-dibrom-2-metoksiacetofenon : prekursori u sintetički korisnim transformacijama iniciranim retkim halofilnim napadom nukleofila.” 2014. Web. 07 Mar 2021.

Vancouver:

Aleksić J1. 4-oksotiazolidin-2-alkiliden vinil-bromidi i α, α-dibrom-2-metoksiacetofenon : prekursori u sintetički korisnim transformacijama iniciranim retkim halofilnim napadom nukleofila. [Internet] [Thesis]. Univerzitet u Beogradu; 2014. [cited 2021 Mar 07]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:8119/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:

Aleksić J1. 4-oksotiazolidin-2-alkiliden vinil-bromidi i α, α-dibrom-2-metoksiacetofenon : prekursori u sintetički korisnim transformacijama iniciranim retkim halofilnim napadom nukleofila. [Thesis]. Univerzitet u Beogradu; 2014. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:8119/bdef:Content/get

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


Iowa State University

19. Luan, Xuechen. Layered double hydroxide-derived nanomaterials for Suzuki−Miyaura cross-coupling reaction.

Degree: 2019, Iowa State University

 Layered double hydroxide (LDH) is an inorganic solid with a brucite-like structure that is similar to hydrotalcite, which contains two main metal plates and an… (more)

Subjects/Keywords: Layered double hydroxide; Room temperature; Single atom Palladium; Suzuki coupling reaction; Chemistry

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APA (6th Edition):

Luan, X. (2019). Layered double hydroxide-derived nanomaterials for Suzuki−Miyaura cross-coupling reaction. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/17735

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):

Luan, Xuechen. “Layered double hydroxide-derived nanomaterials for Suzuki−Miyaura cross-coupling reaction.” 2019. Thesis, Iowa State University. Accessed March 07, 2021. https://lib.dr.iastate.edu/etd/17735.

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

MLA Handbook (7th Edition):

Luan, Xuechen. “Layered double hydroxide-derived nanomaterials for Suzuki−Miyaura cross-coupling reaction.” 2019. Web. 07 Mar 2021.

Vancouver:

Luan X. Layered double hydroxide-derived nanomaterials for Suzuki−Miyaura cross-coupling reaction. [Internet] [Thesis]. Iowa State University; 2019. [cited 2021 Mar 07]. Available from: https://lib.dr.iastate.edu/etd/17735.

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

Council of Science Editors:

Luan X. Layered double hydroxide-derived nanomaterials for Suzuki−Miyaura cross-coupling reaction. [Thesis]. Iowa State University; 2019. Available from: https://lib.dr.iastate.edu/etd/17735

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


Virginia Commonwealth University

20. Brinkley, Kendra W. The Synthesis of Solid Supported Palladium Nanoparticles: Effective Catalysts for Batch and Continuous Cross Coupling Reactions.

Degree: PhD, Engineering, 2015, Virginia Commonwealth University

  Catalysis is one of the pillars of the chemical industry. While the use of catalyst is typically recognized in the automobile industry, their impact… (more)

Subjects/Keywords: Palladium nanoparticles; Suzuki Reaction; graphene; Catalysis; Continuous Reactions; Carbon nanotubes; Catalysis and Reaction Engineering; Process Control and Systems

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APA (6th Edition):

Brinkley, K. W. (2015). The Synthesis of Solid Supported Palladium Nanoparticles: Effective Catalysts for Batch and Continuous Cross Coupling Reactions. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/ND17-CM26 ; https://scholarscompass.vcu.edu/etd/3959

Chicago Manual of Style (16th Edition):

Brinkley, Kendra W. “The Synthesis of Solid Supported Palladium Nanoparticles: Effective Catalysts for Batch and Continuous Cross Coupling Reactions.” 2015. Doctoral Dissertation, Virginia Commonwealth University. Accessed March 07, 2021. https://doi.org/10.25772/ND17-CM26 ; https://scholarscompass.vcu.edu/etd/3959.

MLA Handbook (7th Edition):

Brinkley, Kendra W. “The Synthesis of Solid Supported Palladium Nanoparticles: Effective Catalysts for Batch and Continuous Cross Coupling Reactions.” 2015. Web. 07 Mar 2021.

Vancouver:

Brinkley KW. The Synthesis of Solid Supported Palladium Nanoparticles: Effective Catalysts for Batch and Continuous Cross Coupling Reactions. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2015. [cited 2021 Mar 07]. Available from: https://doi.org/10.25772/ND17-CM26 ; https://scholarscompass.vcu.edu/etd/3959.

Council of Science Editors:

Brinkley KW. The Synthesis of Solid Supported Palladium Nanoparticles: Effective Catalysts for Batch and Continuous Cross Coupling Reactions. [Doctoral Dissertation]. Virginia Commonwealth University; 2015. Available from: https://doi.org/10.25772/ND17-CM26 ; https://scholarscompass.vcu.edu/etd/3959

21. Peramo, Arnaud. Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction.

Degree: Docteur es, Pharmacotechnie et biopharmacie, 2019, Université Paris-Saclay (ComUE)

Les nanotechnologies ont ouvert de nouvelles perspectives pour l’administration ciblée des médicaments. Les approches actuelles en nanomédecine sont basées sur l’encapsulation d’un principe actif dans… (more)

Subjects/Keywords: Palladium nanoparticules; Réaction de Suzuki-Myaura; Chimie in vivo; Thyroglobuline; Protémoque; Palladium nanoparticles; Suzuki-Myaura cross-Coupling reaction; In vivo chemistry; Thyroglobulin; Proteomic

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APA (6th Edition):

Peramo, A. (2019). Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS600

Chicago Manual of Style (16th Edition):

Peramo, Arnaud. “Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed March 07, 2021. http://www.theses.fr/2019SACLS600.

MLA Handbook (7th Edition):

Peramo, Arnaud. “Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction.” 2019. Web. 07 Mar 2021.

Vancouver:

Peramo A. Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2021 Mar 07]. Available from: http://www.theses.fr/2019SACLS600.

Council of Science Editors:

Peramo A. Modification sélective de protéines en milieu biologique par réaction de Suzuki-Miyaura nanocatalysée : Selective modification of a protein in biological media by nanocatalyzed Suzuki-Miyaura reaction. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS600


University of Victoria

22. Yunker, Lars Peter Erasmus. Real-time mass spectrometric analysis of catalytic reaction mechanisms.

Degree: Department of Chemistry, 2017, University of Victoria

 Mass spectrometry was used to study two disparate transformations: in an applied project, the supposed degradation of perfluorooctanesulfonate (PFOS); and in a fundamental study, the… (more)

Subjects/Keywords: Mass spectrometry; Suzuki-Miyaura; online reaction monitoring; electrospray ionization; ESI-MS; perfluorooctane sulfonate; PFOS; transmetallation mechanism; trifluoroborate hydrolysis; suzuki polycondensation; python; MSPT; pressurized sample infusion

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APA (6th Edition):

Yunker, L. P. E. (2017). Real-time mass spectrometric analysis of catalytic reaction mechanisms. (Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/8029

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):

Yunker, Lars Peter Erasmus. “Real-time mass spectrometric analysis of catalytic reaction mechanisms.” 2017. Thesis, University of Victoria. Accessed March 07, 2021. http://hdl.handle.net/1828/8029.

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

MLA Handbook (7th Edition):

Yunker, Lars Peter Erasmus. “Real-time mass spectrometric analysis of catalytic reaction mechanisms.” 2017. Web. 07 Mar 2021.

Vancouver:

Yunker LPE. Real-time mass spectrometric analysis of catalytic reaction mechanisms. [Internet] [Thesis]. University of Victoria; 2017. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1828/8029.

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

Council of Science Editors:

Yunker LPE. Real-time mass spectrometric analysis of catalytic reaction mechanisms. [Thesis]. University of Victoria; 2017. Available from: http://hdl.handle.net/1828/8029

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


Pontifical Catholic University of Rio de Janeiro

23. [No author]. [en] BAMBOO LIGNOCELLULOSIC SUPPORT IMPREGNATED WITH PALLADIUM AND ITS APPLICATION FOR SUZUKI REACTION.

Degree: 2021, Pontifical Catholic University of Rio de Janeiro

[pt] A reação de acoplamento C-C de Suzuki, desde a sua descoberta, sempre atraiu o interesse de diversos pesquisadores e encontrou aplicação em diversos campos… (more)

Subjects/Keywords: [pt] BAMBU; [pt] REACAO DE SUZUKI; [pt] NANOPARTICULAS DE PALADIO; [pt] CATALISE HETEROGENEA; [en] BAMBOO; [en] SUZUKI REACTION; [en] PALLADIUM NANOPARTICLES; [en] HETEROGENEOUS CATALYSIS

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APA (6th Edition):

author], [. (2021). [en] BAMBOO LIGNOCELLULOSIC SUPPORT IMPREGNATED WITH PALLADIUM AND ITS APPLICATION FOR SUZUKI REACTION. (Thesis). Pontifical Catholic University of Rio de Janeiro. Retrieved from http://www.maxwell.vrac.puc-rio.br/Busca_etds.php?strSecao=resultado&nrSeq=51181

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):

author], [No. “[en] BAMBOO LIGNOCELLULOSIC SUPPORT IMPREGNATED WITH PALLADIUM AND ITS APPLICATION FOR SUZUKI REACTION.” 2021. Thesis, Pontifical Catholic University of Rio de Janeiro. Accessed March 07, 2021. http://www.maxwell.vrac.puc-rio.br/Busca_etds.php?strSecao=resultado&nrSeq=51181.

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

MLA Handbook (7th Edition):

author], [No. “[en] BAMBOO LIGNOCELLULOSIC SUPPORT IMPREGNATED WITH PALLADIUM AND ITS APPLICATION FOR SUZUKI REACTION.” 2021. Web. 07 Mar 2021.

Vancouver:

author] [. [en] BAMBOO LIGNOCELLULOSIC SUPPORT IMPREGNATED WITH PALLADIUM AND ITS APPLICATION FOR SUZUKI REACTION. [Internet] [Thesis]. Pontifical Catholic University of Rio de Janeiro; 2021. [cited 2021 Mar 07]. Available from: http://www.maxwell.vrac.puc-rio.br/Busca_etds.php?strSecao=resultado&nrSeq=51181.

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

Council of Science Editors:

author] [. [en] BAMBOO LIGNOCELLULOSIC SUPPORT IMPREGNATED WITH PALLADIUM AND ITS APPLICATION FOR SUZUKI REACTION. [Thesis]. Pontifical Catholic University of Rio de Janeiro; 2021. Available from: http://www.maxwell.vrac.puc-rio.br/Busca_etds.php?strSecao=resultado&nrSeq=51181

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

24. D'Attoma, Joseph. Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction.

Degree: Docteur es, Chimie, 2013, Université Claude Bernard – Lyon I

Les lymphomes à grandes cellules anaplasiques ou ALCL (Anaplastic Large-Cell Lymphoma) sont des cancers appartenant à la famille des lymphomes de type non-Hodgkin. La majorité… (more)

Subjects/Keywords: 2-acylaminothiazoles; Restriction calorique; ALCL; NPM-ALK; Réaction de Suzuki- Miyaura; Réaction de Buchwald-Hartwig; Réaction de Sonogashira; 2-acylaminothiazols; Caloric restriction; ALCL; NPM-ALK; Suzuki-Miyaura crosscoupling reaction; Buchwald-Hartwig cross-coupling reaction; Sonogashira cross-coupling reaction; 547

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APA (6th Edition):

D'Attoma, J. (2013). Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2013LYO10243

Chicago Manual of Style (16th Edition):

D'Attoma, Joseph. “Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction.” 2013. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed March 07, 2021. http://www.theses.fr/2013LYO10243.

MLA Handbook (7th Edition):

D'Attoma, Joseph. “Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction.” 2013. Web. 07 Mar 2021.

Vancouver:

D'Attoma J. Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2013. [cited 2021 Mar 07]. Available from: http://www.theses.fr/2013LYO10243.

Council of Science Editors:

D'Attoma J. Conception, synthèses et évaluations biologiques d’inhibiteurs à double cible : ALK et la restriction calorique : Design, synthesis and biological evaluations of inhibitors double target : ALK and caloric restriction. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2013. Available from: http://www.theses.fr/2013LYO10243


NSYSU

25. Li, Yi-wei. Aggregation-Induced Emission Enhancement of organic and polymeric fluorophores containing 2,4,6-Triphenylpyridine moiety.

Degree: Master, Materials and Optoelectronic Science, 2012, NSYSU

 In this study, organic and polymeric fluorophores based on 2,4,6-triphenylpyridiene (TPP) structure were found to have the novel aggregation-induced emission enhancement (AIEE) property. For the… (more)

Subjects/Keywords: 6-triphenylpyridiene; 4; quantum yield (ФF); suzuki coupling; 2; Chichibabin reaction; aggregation-induced emission enhancement (AIEE); crystallization-induced emission enhancement (CIEE)

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APA (6th Edition):

Li, Y. (2012). Aggregation-Induced Emission Enhancement of organic and polymeric fluorophores containing 2,4,6-Triphenylpyridine moiety. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0713112-173820

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):

Li, Yi-wei. “Aggregation-Induced Emission Enhancement of organic and polymeric fluorophores containing 2,4,6-Triphenylpyridine moiety.” 2012. Thesis, NSYSU. Accessed March 07, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0713112-173820.

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

MLA Handbook (7th Edition):

Li, Yi-wei. “Aggregation-Induced Emission Enhancement of organic and polymeric fluorophores containing 2,4,6-Triphenylpyridine moiety.” 2012. Web. 07 Mar 2021.

Vancouver:

Li Y. Aggregation-Induced Emission Enhancement of organic and polymeric fluorophores containing 2,4,6-Triphenylpyridine moiety. [Internet] [Thesis]. NSYSU; 2012. [cited 2021 Mar 07]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0713112-173820.

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

Council of Science Editors:

Li Y. Aggregation-Induced Emission Enhancement of organic and polymeric fluorophores containing 2,4,6-Triphenylpyridine moiety. [Thesis]. NSYSU; 2012. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0713112-173820

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

26. 贾, 吉祥. Development of highly effective reaction system using supported Pd catalysts for the Suzuki-Miyaura coupling of bromobenzene and chlorobenzene with phenylboronic acid.

Degree: Japan Advanced Institute of Science and Technology / 北陸先端科学技術大学院大学

Supervisor:海老谷 幸喜

マテリアルサイエンス研究科

修士

Subjects/Keywords: Suzuki-Miyaura coupling reaction; Palladium; Hydrotalcite; Mgnesium hydroxide; Surfactant

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APA (6th Edition):

贾, . (n.d.). Development of highly effective reaction system using supported Pd catalysts for the Suzuki-Miyaura coupling of bromobenzene and chlorobenzene with phenylboronic acid. (Thesis). Japan Advanced Institute of Science and Technology / 北陸先端科学技術大学院大学. Retrieved from http://hdl.handle.net/10119/11940

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

贾, 吉祥. “Development of highly effective reaction system using supported Pd catalysts for the Suzuki-Miyaura coupling of bromobenzene and chlorobenzene with phenylboronic acid.” Thesis, Japan Advanced Institute of Science and Technology / 北陸先端科学技術大学院大学. Accessed March 07, 2021. http://hdl.handle.net/10119/11940.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

贾, 吉祥. “Development of highly effective reaction system using supported Pd catalysts for the Suzuki-Miyaura coupling of bromobenzene and chlorobenzene with phenylboronic acid.” Web. 07 Mar 2021.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

贾 . Development of highly effective reaction system using supported Pd catalysts for the Suzuki-Miyaura coupling of bromobenzene and chlorobenzene with phenylboronic acid. [Internet] [Thesis]. Japan Advanced Institute of Science and Technology / 北陸先端科学技術大学院大学; [cited 2021 Mar 07]. Available from: http://hdl.handle.net/10119/11940.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

贾 . Development of highly effective reaction system using supported Pd catalysts for the Suzuki-Miyaura coupling of bromobenzene and chlorobenzene with phenylboronic acid. [Thesis]. Japan Advanced Institute of Science and Technology / 北陸先端科学技術大学院大学; Available from: http://hdl.handle.net/10119/11940

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


University of the Western Cape

27. Ramoroka, Morongwa Emmanuel. Photophysics of Thiophenosalicylaldimine-functionalized G1-Polyprolyleniminato-Copper Telluride/Antimonide core-shell Nanomaterials .

Degree: 2018, University of the Western Cape

 This work involves the synthesis of copper telluride-polypropylenimine tetra(5-(2-thienyl) salicylaldimine) ([email protected]) and copper antimonide-polypropylenimine tetra(5-(2-thienyl) salicylaldimine) ([email protected]) core-shell nanoparticles (NPs), using two-pots and one-pot synthesis… (more)

Subjects/Keywords: Bimetallic nanoparticles; Metal-chalcogenides nanoparticles; Dendrimers; Core-shell nanoparticles; Photophysics; Photovoltaics; Electrochemical characterization; Schiff base condensation; Chemical reduction; Suzuki coupling reaction

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APA (6th Edition):

Ramoroka, M. E. (2018). Photophysics of Thiophenosalicylaldimine-functionalized G1-Polyprolyleniminato-Copper Telluride/Antimonide core-shell Nanomaterials . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/6262

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):

Ramoroka, Morongwa Emmanuel. “Photophysics of Thiophenosalicylaldimine-functionalized G1-Polyprolyleniminato-Copper Telluride/Antimonide core-shell Nanomaterials .” 2018. Thesis, University of the Western Cape. Accessed March 07, 2021. http://hdl.handle.net/11394/6262.

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

MLA Handbook (7th Edition):

Ramoroka, Morongwa Emmanuel. “Photophysics of Thiophenosalicylaldimine-functionalized G1-Polyprolyleniminato-Copper Telluride/Antimonide core-shell Nanomaterials .” 2018. Web. 07 Mar 2021.

Vancouver:

Ramoroka ME. Photophysics of Thiophenosalicylaldimine-functionalized G1-Polyprolyleniminato-Copper Telluride/Antimonide core-shell Nanomaterials . [Internet] [Thesis]. University of the Western Cape; 2018. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/11394/6262.

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

Council of Science Editors:

Ramoroka ME. Photophysics of Thiophenosalicylaldimine-functionalized G1-Polyprolyleniminato-Copper Telluride/Antimonide core-shell Nanomaterials . [Thesis]. University of the Western Cape; 2018. Available from: http://hdl.handle.net/11394/6262

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

28. Abou Hamdan, Hussein. Synthèse de nouveaux agents anticancéreux : Synthesis of new anticancer agents.

Degree: Docteur es, Chimie, 2018, Université de Strasbourg

Les cancers représentent un problème majeur de santé public d'où la nécessité de rechercher de nouvelles classes de médicaments. Parmi les pistes pour développer de… (more)

Subjects/Keywords: Modulateurs d'épissage; NVS-SM2; Pyridazine; Flavagline; Chimie hétérocyclique; Splicing modulators; NVS-SM2; Pyridazine; Suzuki-Miyaura reaction; Flavaglines; KRAS; Heterocyclic chemistry

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

APA (6th Edition):

Abou Hamdan, H. (2018). Synthèse de nouveaux agents anticancéreux : Synthesis of new anticancer agents. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2018STRAF012

Chicago Manual of Style (16th Edition):

Abou Hamdan, Hussein. “Synthèse de nouveaux agents anticancéreux : Synthesis of new anticancer agents.” 2018. Doctoral Dissertation, Université de Strasbourg. Accessed March 07, 2021. http://www.theses.fr/2018STRAF012.

MLA Handbook (7th Edition):

Abou Hamdan, Hussein. “Synthèse de nouveaux agents anticancéreux : Synthesis of new anticancer agents.” 2018. Web. 07 Mar 2021.

Vancouver:

Abou Hamdan H. Synthèse de nouveaux agents anticancéreux : Synthesis of new anticancer agents. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2018. [cited 2021 Mar 07]. Available from: http://www.theses.fr/2018STRAF012.

Council of Science Editors:

Abou Hamdan H. Synthèse de nouveaux agents anticancéreux : Synthesis of new anticancer agents. [Doctoral Dissertation]. Université de Strasbourg; 2018. Available from: http://www.theses.fr/2018STRAF012


Universitat de Girona

29. Ng Choi, I-teng Montserrat. Solid-phase synthesis of 5-arylhistidine-containing peptides: from linear antimicrobial peptides to cyclic peptides derived from arylomycins and aciculitins.

Degree: Departament de Química, 2015, Universitat de Girona

 La incorporació de sistemes biarílics asimiètrics en seqüències peptídiques es considera un enfocament útil per a millorar l'activitat biològica de pèptids. Tenint en compte la… (more)

Subjects/Keywords: Histidine; Histidina; Biaryl peptides; Pèptids biarílics; Péptidos biarílicos; Microwave irradiation; Irradiació de microones; Irradiación de microondas; Macroarylation; Macroarilació; Macroarilación; Arylomycins; Arilomicines; Arilomicinas; Suzuki-Miyaura reaction; Reacción Suzuki-Miyaura; Reacció Suzuki-Miyaura; 547

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APA (6th Edition):

Ng Choi, I. M. (2015). Solid-phase synthesis of 5-arylhistidine-containing peptides: from linear antimicrobial peptides to cyclic peptides derived from arylomycins and aciculitins. (Thesis). Universitat de Girona. Retrieved from http://hdl.handle.net/10803/380739

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):

Ng Choi, I-teng Montserrat. “Solid-phase synthesis of 5-arylhistidine-containing peptides: from linear antimicrobial peptides to cyclic peptides derived from arylomycins and aciculitins.” 2015. Thesis, Universitat de Girona. Accessed March 07, 2021. http://hdl.handle.net/10803/380739.

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

MLA Handbook (7th Edition):

Ng Choi, I-teng Montserrat. “Solid-phase synthesis of 5-arylhistidine-containing peptides: from linear antimicrobial peptides to cyclic peptides derived from arylomycins and aciculitins.” 2015. Web. 07 Mar 2021.

Vancouver:

Ng Choi IM. Solid-phase synthesis of 5-arylhistidine-containing peptides: from linear antimicrobial peptides to cyclic peptides derived from arylomycins and aciculitins. [Internet] [Thesis]. Universitat de Girona; 2015. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/10803/380739.

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

Council of Science Editors:

Ng Choi IM. Solid-phase synthesis of 5-arylhistidine-containing peptides: from linear antimicrobial peptides to cyclic peptides derived from arylomycins and aciculitins. [Thesis]. Universitat de Girona; 2015. Available from: http://hdl.handle.net/10803/380739

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


Universitat de Girona

30. Afonso Afonso, Ana. Pèptids biarílics a partir de 4-iodofenilalanina o 3-iodotirosina per borilació i reacció de Suzuki-Miyaura en fase sòlida. Avaluació de l'activitat antimicrobiana.

Degree: Departament de Química, 2011, Universitat de Girona

 The present PhD study was focused on the preparation of biaryl peptides on solid-phase. First, phenylalanine or tyrosine residues were borylated through a Miyaura reaction.… (more)

Subjects/Keywords: Pèptids biarílics; Biaryl peptides; Péptidos biarílicos; Pèptids antimicrobials; Antimicrobial peptides; Péptidos antimicrobianos; Irradiació de microones; Microwave irradiation; Irradiación de microondas; Fase sòlida; Solid-phase; Fase sólida; Borilació; Borilation; Borilación; Reacció de Suzuki-Miyaura; Suzuki-Miyaura reaction; Reacción de Suzuki-Miyaura; 547

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APA (6th Edition):

Afonso Afonso, A. (2011). Pèptids biarílics a partir de 4-iodofenilalanina o 3-iodotirosina per borilació i reacció de Suzuki-Miyaura en fase sòlida. Avaluació de l'activitat antimicrobiana. (Thesis). Universitat de Girona. Retrieved from http://hdl.handle.net/10803/38882

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):

Afonso Afonso, Ana. “Pèptids biarílics a partir de 4-iodofenilalanina o 3-iodotirosina per borilació i reacció de Suzuki-Miyaura en fase sòlida. Avaluació de l'activitat antimicrobiana.” 2011. Thesis, Universitat de Girona. Accessed March 07, 2021. http://hdl.handle.net/10803/38882.

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

MLA Handbook (7th Edition):

Afonso Afonso, Ana. “Pèptids biarílics a partir de 4-iodofenilalanina o 3-iodotirosina per borilació i reacció de Suzuki-Miyaura en fase sòlida. Avaluació de l'activitat antimicrobiana.” 2011. Web. 07 Mar 2021.

Vancouver:

Afonso Afonso A. Pèptids biarílics a partir de 4-iodofenilalanina o 3-iodotirosina per borilació i reacció de Suzuki-Miyaura en fase sòlida. Avaluació de l'activitat antimicrobiana. [Internet] [Thesis]. Universitat de Girona; 2011. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/10803/38882.

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

Council of Science Editors:

Afonso Afonso A. Pèptids biarílics a partir de 4-iodofenilalanina o 3-iodotirosina per borilació i reacció de Suzuki-Miyaura en fase sòlida. Avaluació de l'activitat antimicrobiana. [Thesis]. Universitat de Girona; 2011. Available from: http://hdl.handle.net/10803/38882

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

[1] [2]

.