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You searched for subject:(Direct arylation). Showing records 1 – 30 of 30 total matches.

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University of Ottawa

1. Petrov, Ivan. The Impact of Chlorine Substituents on the Regioselectivity of Pd(0)-catalyzed Direct Arylation of Heteroaromatics .

Degree: 2011, University of Ottawa

 The regioselectivity in Pd(0)-catalyzed direct arylation of pyrrole, thiophene, and indole can be improved by blocking some of the reactive sites with a chloride group,… (more)

Subjects/Keywords: direct arylation; chlorination; heteroaromatics; palladium catalysis

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

APA (6th Edition):

Petrov, I. (2011). The Impact of Chlorine Substituents on the Regioselectivity of Pd(0)-catalyzed Direct Arylation of Heteroaromatics . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/19788

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):

Petrov, Ivan. “The Impact of Chlorine Substituents on the Regioselectivity of Pd(0)-catalyzed Direct Arylation of Heteroaromatics .” 2011. Thesis, University of Ottawa. Accessed January 27, 2021. http://hdl.handle.net/10393/19788.

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

MLA Handbook (7th Edition):

Petrov, Ivan. “The Impact of Chlorine Substituents on the Regioselectivity of Pd(0)-catalyzed Direct Arylation of Heteroaromatics .” 2011. Web. 27 Jan 2021.

Vancouver:

Petrov I. The Impact of Chlorine Substituents on the Regioselectivity of Pd(0)-catalyzed Direct Arylation of Heteroaromatics . [Internet] [Thesis]. University of Ottawa; 2011. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/10393/19788.

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

Council of Science Editors:

Petrov I. The Impact of Chlorine Substituents on the Regioselectivity of Pd(0)-catalyzed Direct Arylation of Heteroaromatics . [Thesis]. University of Ottawa; 2011. Available from: http://hdl.handle.net/10393/19788

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


Universitat Rovira i Virgili

2. de Mendoza Bonmatí, Paula. Design and synthesis of new polyaromatic scaffolds for nano-scale applications.

Degree: Departament de Química Analítica i Química Orgànica, 2010, Universitat Rovira i Virgili

 Design and Synthesis of New Polyaromatic Scaffolds for Nano-Scale Applications Resumen: En la última década, el diseño y la síntesis de nuevos sistemas poliaromáticos han… (more)

Subjects/Keywords: Molecular Electronics; Direct Arylation; PAHs; 542; 547

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APA (6th Edition):

de Mendoza Bonmatí, P. (2010). Design and synthesis of new polyaromatic scaffolds for nano-scale applications. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/9045

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):

de Mendoza Bonmatí, Paula. “Design and synthesis of new polyaromatic scaffolds for nano-scale applications.” 2010. Thesis, Universitat Rovira i Virgili. Accessed January 27, 2021. http://hdl.handle.net/10803/9045.

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

MLA Handbook (7th Edition):

de Mendoza Bonmatí, Paula. “Design and synthesis of new polyaromatic scaffolds for nano-scale applications.” 2010. Web. 27 Jan 2021.

Vancouver:

de Mendoza Bonmatí P. Design and synthesis of new polyaromatic scaffolds for nano-scale applications. [Internet] [Thesis]. Universitat Rovira i Virgili; 2010. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/10803/9045.

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

Council of Science Editors:

de Mendoza Bonmatí P. Design and synthesis of new polyaromatic scaffolds for nano-scale applications. [Thesis]. Universitat Rovira i Virgili; 2010. Available from: http://hdl.handle.net/10803/9045

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


University College Cork

3. Shanahan, Rachel. Synthesis of nitrogen-containing heterocycles.

Degree: 2019, University College Cork

 The sharp rise in antimicrobial resistance has been matched by a decline in the identification and clinical introduction of new classes of drugs to treat… (more)

Subjects/Keywords: Synthesis; Direct arylation; Total synthesis; Quinolone; Quinoline

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APA (6th Edition):

Shanahan, R. (2019). Synthesis of nitrogen-containing heterocycles. (Thesis). University College Cork. Retrieved from http://hdl.handle.net/10468/10087

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):

Shanahan, Rachel. “Synthesis of nitrogen-containing heterocycles.” 2019. Thesis, University College Cork. Accessed January 27, 2021. http://hdl.handle.net/10468/10087.

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

MLA Handbook (7th Edition):

Shanahan, Rachel. “Synthesis of nitrogen-containing heterocycles.” 2019. Web. 27 Jan 2021.

Vancouver:

Shanahan R. Synthesis of nitrogen-containing heterocycles. [Internet] [Thesis]. University College Cork; 2019. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/10468/10087.

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

Council of Science Editors:

Shanahan R. Synthesis of nitrogen-containing heterocycles. [Thesis]. University College Cork; 2019. Available from: http://hdl.handle.net/10468/10087

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


University of Southern California

4. Rudenko, Andrey E. Direct arylation polymerization (DARP) for the synthesis of conjugated polymers.

Degree: PhD, Chemistry, 2014, University of Southern California

Direct Arylation Polymerization (DArP) has emerged recently as a C-H activation method of synthesis for conjugated polymers. It represents an attractive alternative to traditional methods… (more)

Subjects/Keywords: conjugated polymer; structure; defects; direct arylation

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

APA (6th Edition):

Rudenko, A. E. (2014). Direct arylation polymerization (DARP) for the synthesis of conjugated polymers. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/419336/rec/2011

Chicago Manual of Style (16th Edition):

Rudenko, Andrey E. “Direct arylation polymerization (DARP) for the synthesis of conjugated polymers.” 2014. Doctoral Dissertation, University of Southern California. Accessed January 27, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/419336/rec/2011.

MLA Handbook (7th Edition):

Rudenko, Andrey E. “Direct arylation polymerization (DARP) for the synthesis of conjugated polymers.” 2014. Web. 27 Jan 2021.

Vancouver:

Rudenko AE. Direct arylation polymerization (DARP) for the synthesis of conjugated polymers. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2021 Jan 27]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/419336/rec/2011.

Council of Science Editors:

Rudenko AE. Direct arylation polymerization (DARP) for the synthesis of conjugated polymers. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/419336/rec/2011


Georgia Tech

5. Ponder, James. A Pedot by any other name: Tuning the electroactivity of dioxy-heterocycles for redox and solid state applications.

Degree: PhD, Chemistry and Biochemistry, 2017, Georgia Tech

 Redox active conjugated polymers are used in a variety of applications including electrochromism, charge storage, plasmonic resonance tuning, and electrochemical transistors. This thesis describes the… (more)

Subjects/Keywords: Conjugated polymers; Dioxythiophene; Supercapacitor; Electrochromism; Direct arylation

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APA (6th Edition):

Ponder, J. (2017). A Pedot by any other name: Tuning the electroactivity of dioxy-heterocycles for redox and solid state applications. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60158

Chicago Manual of Style (16th Edition):

Ponder, James. “A Pedot by any other name: Tuning the electroactivity of dioxy-heterocycles for redox and solid state applications.” 2017. Doctoral Dissertation, Georgia Tech. Accessed January 27, 2021. http://hdl.handle.net/1853/60158.

MLA Handbook (7th Edition):

Ponder, James. “A Pedot by any other name: Tuning the electroactivity of dioxy-heterocycles for redox and solid state applications.” 2017. Web. 27 Jan 2021.

Vancouver:

Ponder J. A Pedot by any other name: Tuning the electroactivity of dioxy-heterocycles for redox and solid state applications. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/1853/60158.

Council of Science Editors:

Ponder J. A Pedot by any other name: Tuning the electroactivity of dioxy-heterocycles for redox and solid state applications. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/60158


Georgia Tech

6. Deininger, James J. Synthesis of pi conjugated polymers for use in photovoltaic and electrochromic applications.

Degree: MS, Chemistry and Biochemistry, 2015, Georgia Tech

 Conjugated polymers are currently being used for a wide range of electronic applications. In this thesis, we studied two different synthetic approaches that lead to… (more)

Subjects/Keywords: Polymer; Elctrochromic; Conjugated polymer; Dithienogermole; Photovoltaic; Direct (hetero)arylation; Direct arylation; Polymerizations; 3,4-propylenedioxythiophene

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APA (6th Edition):

Deininger, J. J. (2015). Synthesis of pi conjugated polymers for use in photovoltaic and electrochromic applications. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53873

Chicago Manual of Style (16th Edition):

Deininger, James J. “Synthesis of pi conjugated polymers for use in photovoltaic and electrochromic applications.” 2015. Masters Thesis, Georgia Tech. Accessed January 27, 2021. http://hdl.handle.net/1853/53873.

MLA Handbook (7th Edition):

Deininger, James J. “Synthesis of pi conjugated polymers for use in photovoltaic and electrochromic applications.” 2015. Web. 27 Jan 2021.

Vancouver:

Deininger JJ. Synthesis of pi conjugated polymers for use in photovoltaic and electrochromic applications. [Internet] [Masters thesis]. Georgia Tech; 2015. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/1853/53873.

Council of Science Editors:

Deininger JJ. Synthesis of pi conjugated polymers for use in photovoltaic and electrochromic applications. [Masters Thesis]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/53873


Universiteit Utrecht

7. 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 January 27, 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. 27 Jan 2021.

Vancouver:

Huang Y. Practical catalytic arylation of C–H bonds by iron/phenanthroline systems. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2015. [cited 2021 Jan 27]. 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 Ottawa

8. Sun, Ho-Yan. Studies on the Mechanism of Direct Arylation of Pyridine N oxides: Evidence for the Essential Involvement of Acetate from the Pd(OAc)2 Pre-Catalyst at the C-H Bond Cleaving Step .

Degree: 2011, University of Ottawa

 Detailed mechanistic studies on the palladium-catalyzed direct arylation of pyridine N-oxides are presented. The order of each reaction component is determined to provide a general… (more)

Subjects/Keywords: N-Oxide; Palladium; Catalytic Direct Arylation; Mechanism; Concerted Metallation-Deprotonation

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APA (6th Edition):

Sun, H. (2011). Studies on the Mechanism of Direct Arylation of Pyridine N oxides: Evidence for the Essential Involvement of Acetate from the Pd(OAc)2 Pre-Catalyst at the C-H Bond Cleaving Step . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/19760

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):

Sun, Ho-Yan. “Studies on the Mechanism of Direct Arylation of Pyridine N oxides: Evidence for the Essential Involvement of Acetate from the Pd(OAc)2 Pre-Catalyst at the C-H Bond Cleaving Step .” 2011. Thesis, University of Ottawa. Accessed January 27, 2021. http://hdl.handle.net/10393/19760.

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

MLA Handbook (7th Edition):

Sun, Ho-Yan. “Studies on the Mechanism of Direct Arylation of Pyridine N oxides: Evidence for the Essential Involvement of Acetate from the Pd(OAc)2 Pre-Catalyst at the C-H Bond Cleaving Step .” 2011. Web. 27 Jan 2021.

Vancouver:

Sun H. Studies on the Mechanism of Direct Arylation of Pyridine N oxides: Evidence for the Essential Involvement of Acetate from the Pd(OAc)2 Pre-Catalyst at the C-H Bond Cleaving Step . [Internet] [Thesis]. University of Ottawa; 2011. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/10393/19760.

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

Council of Science Editors:

Sun H. Studies on the Mechanism of Direct Arylation of Pyridine N oxides: Evidence for the Essential Involvement of Acetate from the Pd(OAc)2 Pre-Catalyst at the C-H Bond Cleaving Step . [Thesis]. University of Ottawa; 2011. Available from: http://hdl.handle.net/10393/19760

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


University of Manitoba

9. Geary, Laina Michelle. A diversity-oriented approach to the palladium-catalyzed modular assembly of conjugated compounds and heterocycles: high-value compounds from trichloroethylene.

Degree: Chemistry, 2011, University of Manitoba

 Trichloroethylene, a simple and very inexpensive material, has been identified as a tri- and tetrafunctionalizable building block. A combination of selective palladium-catalyzed cross-coupling reactions with… (more)

Subjects/Keywords: palladium; heterocycles; direct arylation; cross-coupling; boronic acids; trichloroethylene

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APA (6th Edition):

Geary, L. M. (2011). A diversity-oriented approach to the palladium-catalyzed modular assembly of conjugated compounds and heterocycles: high-value compounds from trichloroethylene. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/4381

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):

Geary, Laina Michelle. “A diversity-oriented approach to the palladium-catalyzed modular assembly of conjugated compounds and heterocycles: high-value compounds from trichloroethylene.” 2011. Thesis, University of Manitoba. Accessed January 27, 2021. http://hdl.handle.net/1993/4381.

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

MLA Handbook (7th Edition):

Geary, Laina Michelle. “A diversity-oriented approach to the palladium-catalyzed modular assembly of conjugated compounds and heterocycles: high-value compounds from trichloroethylene.” 2011. Web. 27 Jan 2021.

Vancouver:

Geary LM. A diversity-oriented approach to the palladium-catalyzed modular assembly of conjugated compounds and heterocycles: high-value compounds from trichloroethylene. [Internet] [Thesis]. University of Manitoba; 2011. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/1993/4381.

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

Council of Science Editors:

Geary LM. A diversity-oriented approach to the palladium-catalyzed modular assembly of conjugated compounds and heterocycles: high-value compounds from trichloroethylene. [Thesis]. University of Manitoba; 2011. Available from: http://hdl.handle.net/1993/4381

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


INP Toulouse

10. Oukhrib, Abdelouahd. Valorisation des terpènes par formation des nouvelles liaisons C-C et C-X par voie catalytique et hémisynthèse : Terpenes valuation by forming new bonds C-C and C-X by catalytically and hemisynthesis reactions.

Degree: Docteur es, Chimie Organométallique et de Coordination, 2015, INP Toulouse

Transformer des produits naturels, les fonctionnaliser par hémi-synthèse ou par voie catalytique est un outil intéressant pour élargir le spectre des structures accessibles et de… (more)

Subjects/Keywords: Terpènes; Hydroformylation; Ligands phosphorés; Rhodium; Palladium; Arylation directe intramoléculaire; Terpene; Hydroformylation; Phosphorus ligand; Rhodium; Palladium; Intramolecular arylation direct

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APA (6th Edition):

Oukhrib, A. (2015). Valorisation des terpènes par formation des nouvelles liaisons C-C et C-X par voie catalytique et hémisynthèse : Terpenes valuation by forming new bonds C-C and C-X by catalytically and hemisynthesis reactions. (Doctoral Dissertation). INP Toulouse. Retrieved from http://www.theses.fr/2015INPT0029

Chicago Manual of Style (16th Edition):

Oukhrib, Abdelouahd. “Valorisation des terpènes par formation des nouvelles liaisons C-C et C-X par voie catalytique et hémisynthèse : Terpenes valuation by forming new bonds C-C and C-X by catalytically and hemisynthesis reactions.” 2015. Doctoral Dissertation, INP Toulouse. Accessed January 27, 2021. http://www.theses.fr/2015INPT0029.

MLA Handbook (7th Edition):

Oukhrib, Abdelouahd. “Valorisation des terpènes par formation des nouvelles liaisons C-C et C-X par voie catalytique et hémisynthèse : Terpenes valuation by forming new bonds C-C and C-X by catalytically and hemisynthesis reactions.” 2015. Web. 27 Jan 2021.

Vancouver:

Oukhrib A. Valorisation des terpènes par formation des nouvelles liaisons C-C et C-X par voie catalytique et hémisynthèse : Terpenes valuation by forming new bonds C-C and C-X by catalytically and hemisynthesis reactions. [Internet] [Doctoral dissertation]. INP Toulouse; 2015. [cited 2021 Jan 27]. Available from: http://www.theses.fr/2015INPT0029.

Council of Science Editors:

Oukhrib A. Valorisation des terpènes par formation des nouvelles liaisons C-C et C-X par voie catalytique et hémisynthèse : Terpenes valuation by forming new bonds C-C and C-X by catalytically and hemisynthesis reactions. [Doctoral Dissertation]. INP Toulouse; 2015. Available from: http://www.theses.fr/2015INPT0029

11. Naas, Mohammed. Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential.

Degree: Docteur es, Chimie organique. Pharmacochimie, 2016, Orléans; Université Mohamed V

L’accès à de nouveaux composés hétérocycliques originaux biologiquement actifs nécessite la mise au point de nouvelles méthodes de synthèse rapides et efficaces. Dans ce contexte,… (more)

Subjects/Keywords: Indazoles; Suzuki-Miyaura; (hétéro)arylation directe; Alcénylation directe; One-pot; Réactions pallado-catallysées; Indazoles; Suzuki-Miyaura cross-coupling; Direct (hetero)arylation; Direct alkenylation; One-pot; Palladium-catalyzed reactions; 547.59

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APA (6th Edition):

Naas, M. (2016). Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential. (Doctoral Dissertation). Orléans; Université Mohamed V. Retrieved from http://www.theses.fr/2016ORLE2009

Chicago Manual of Style (16th Edition):

Naas, Mohammed. “Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential.” 2016. Doctoral Dissertation, Orléans; Université Mohamed V. Accessed January 27, 2021. http://www.theses.fr/2016ORLE2009.

MLA Handbook (7th Edition):

Naas, Mohammed. “Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential.” 2016. Web. 27 Jan 2021.

Vancouver:

Naas M. Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential. [Internet] [Doctoral dissertation]. Orléans; Université Mohamed V; 2016. [cited 2021 Jan 27]. Available from: http://www.theses.fr/2016ORLE2009.

Council of Science Editors:

Naas M. Synthèse et fonctionnalisation de nouveaux dérivés d’indazoles à visée thérapeutique : Synthesis of new indazoles derivatives with therapeutic potential. [Doctoral Dissertation]. Orléans; Université Mohamed V; 2016. Available from: http://www.theses.fr/2016ORLE2009


Universidade Estadual de Campinas

12. Biajoli, Andre Francisco Pivato, 1978-. Arilação direta de compostos heteroaromáticos com sais de arenodiazônio: SPME (Solid Phase Microextraction) fibers coated with new sol-gel ormosils.

Degree: 2013, Universidade Estadual de Campinas

 Abstract: Aryldiazonium tetrafluoroborates are stable, easy-to-prepare compounds that have been largely employed in Heck-Matsuda reactions, allowing the development of fast, mild and phosphine-free methods. Regarding… (more)

Subjects/Keywords: Arilação direta; Sais de arenodiazônio; Paládio; Heteroaromáticos; Direct arylation; Diazonium salts; Palladium; Heteroaromatics

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APA (6th Edition):

Biajoli, Andre Francisco Pivato, 1. (2013). Arilação direta de compostos heteroaromáticos com sais de arenodiazônio: SPME (Solid Phase Microextraction) fibers coated with new sol-gel ormosils. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/249872

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):

Biajoli, Andre Francisco Pivato, 1978-. “Arilação direta de compostos heteroaromáticos com sais de arenodiazônio: SPME (Solid Phase Microextraction) fibers coated with new sol-gel ormosils.” 2013. Thesis, Universidade Estadual de Campinas. Accessed January 27, 2021. http://repositorio.unicamp.br/jspui/handle/REPOSIP/249872.

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

MLA Handbook (7th Edition):

Biajoli, Andre Francisco Pivato, 1978-. “Arilação direta de compostos heteroaromáticos com sais de arenodiazônio: SPME (Solid Phase Microextraction) fibers coated with new sol-gel ormosils.” 2013. Web. 27 Jan 2021.

Vancouver:

Biajoli, Andre Francisco Pivato 1. Arilação direta de compostos heteroaromáticos com sais de arenodiazônio: SPME (Solid Phase Microextraction) fibers coated with new sol-gel ormosils. [Internet] [Thesis]. Universidade Estadual de Campinas; 2013. [cited 2021 Jan 27]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/249872.

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

Council of Science Editors:

Biajoli, Andre Francisco Pivato 1. Arilação direta de compostos heteroaromáticos com sais de arenodiazônio: SPME (Solid Phase Microextraction) fibers coated with new sol-gel ormosils. [Thesis]. Universidade Estadual de Campinas; 2013. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/249872

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


University of Ottawa

13. Schipper, Derek. Part 1: Transition Metal Catalyzed Functionalization of Aromatic C-H Bonds / Part 2: New Methods in Enantioselective Synthesis .

Degree: 2011, University of Ottawa

 Part 1: Transition-metal-catalyzed direct transformations of aromatic C-H bonds are emerging as valuable tools in organic synthesis. These reactions are attractive because of they allow… (more)

Subjects/Keywords: direct arylation; enantioselective; hydroarylation; kinetic resolution; C-H functionalization; organocatalysis; palladium; rhodium

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APA (6th Edition):

Schipper, D. (2011). Part 1: Transition Metal Catalyzed Functionalization of Aromatic C-H Bonds / Part 2: New Methods in Enantioselective Synthesis . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/20121

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):

Schipper, Derek. “Part 1: Transition Metal Catalyzed Functionalization of Aromatic C-H Bonds / Part 2: New Methods in Enantioselective Synthesis .” 2011. Thesis, University of Ottawa. Accessed January 27, 2021. http://hdl.handle.net/10393/20121.

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

MLA Handbook (7th Edition):

Schipper, Derek. “Part 1: Transition Metal Catalyzed Functionalization of Aromatic C-H Bonds / Part 2: New Methods in Enantioselective Synthesis .” 2011. Web. 27 Jan 2021.

Vancouver:

Schipper D. Part 1: Transition Metal Catalyzed Functionalization of Aromatic C-H Bonds / Part 2: New Methods in Enantioselective Synthesis . [Internet] [Thesis]. University of Ottawa; 2011. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/10393/20121.

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

Council of Science Editors:

Schipper D. Part 1: Transition Metal Catalyzed Functionalization of Aromatic C-H Bonds / Part 2: New Methods in Enantioselective Synthesis . [Thesis]. University of Ottawa; 2011. Available from: http://hdl.handle.net/10393/20121

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

14. Bassoude, Ibtissam. Synthèse de nouveaux dérivés pyrazolo[1,5-a]pyrimidiniques à visée biologique : Synthesis of new pyrazolo[1,5-a]pyrimidinic derivatives aiming at biological activity.

Degree: Docteur es, Chimie, 2012, Orléans; Université Mohammed V-Agdal (Rabat, Maroc)

Nos travaux de thèse portent sur la mise au point de nouvelles méthodes de synthèse permettant l’accès de façon rapide et efficace à différents dérivés… (more)

Subjects/Keywords: Pyrazolo[1,5-a]pyrimidine; Condensation; Pyran-2-one; Micro-onde; (hétéro)arylation directe; Réactions pallado-catalysées; Arylation intramoléculaire; One-pot; Pyrazolo[1,5-a]pyrimidine; Condensation; Pyran-2-one; Microwave; Direct (hetero)arylation; Palladium-catalyzed reactions; Intramolecular arylation; One-pot

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APA (6th Edition):

Bassoude, I. (2012). Synthèse de nouveaux dérivés pyrazolo[1,5-a]pyrimidiniques à visée biologique : Synthesis of new pyrazolo[1,5-a]pyrimidinic derivatives aiming at biological activity. (Doctoral Dissertation). Orléans; Université Mohammed V-Agdal (Rabat, Maroc). Retrieved from http://www.theses.fr/2012ORLE2025

Chicago Manual of Style (16th Edition):

Bassoude, Ibtissam. “Synthèse de nouveaux dérivés pyrazolo[1,5-a]pyrimidiniques à visée biologique : Synthesis of new pyrazolo[1,5-a]pyrimidinic derivatives aiming at biological activity.” 2012. Doctoral Dissertation, Orléans; Université Mohammed V-Agdal (Rabat, Maroc). Accessed January 27, 2021. http://www.theses.fr/2012ORLE2025.

MLA Handbook (7th Edition):

Bassoude, Ibtissam. “Synthèse de nouveaux dérivés pyrazolo[1,5-a]pyrimidiniques à visée biologique : Synthesis of new pyrazolo[1,5-a]pyrimidinic derivatives aiming at biological activity.” 2012. Web. 27 Jan 2021.

Vancouver:

Bassoude I. Synthèse de nouveaux dérivés pyrazolo[1,5-a]pyrimidiniques à visée biologique : Synthesis of new pyrazolo[1,5-a]pyrimidinic derivatives aiming at biological activity. [Internet] [Doctoral dissertation]. Orléans; Université Mohammed V-Agdal (Rabat, Maroc); 2012. [cited 2021 Jan 27]. Available from: http://www.theses.fr/2012ORLE2025.

Council of Science Editors:

Bassoude I. Synthèse de nouveaux dérivés pyrazolo[1,5-a]pyrimidiniques à visée biologique : Synthesis of new pyrazolo[1,5-a]pyrimidinic derivatives aiming at biological activity. [Doctoral Dissertation]. Orléans; Université Mohammed V-Agdal (Rabat, Maroc); 2012. Available from: http://www.theses.fr/2012ORLE2025

15. Zeineddine, Abdallah. Harnessing the reactivity of gold via ligand design : stabilization of reactive intermediates and development of new Au(I)/Au(III) catalytic pathways : Exploitation de la réactivité de l'or via le design des ligands : stabilisation des intermédiaires réactionnels et développement de nouveaux processus catalytiques Au(I)/Au(III).

Degree: Docteur es, Chimie moléculaire, 2017, Université Toulouse III – Paul Sabatier

Ce travail de thèse porte sur la chimie organométallique des complexes d'or(I) et sur l'étude de leurs réactivités. Plus particulièrement, le travail présenté ici dans… (more)

Subjects/Keywords: Chimie de l'or; Addition oxydante; Arylation directe; Carbène a-oxo d'or(I); Gold chemistry; Oxidative addition; Direct arylation; Catalysis; Alpha-oxo gold(I) carbenes

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APA (6th Edition):

Zeineddine, A. (2017). Harnessing the reactivity of gold via ligand design : stabilization of reactive intermediates and development of new Au(I)/Au(III) catalytic pathways : Exploitation de la réactivité de l'or via le design des ligands : stabilisation des intermédiaires réactionnels et développement de nouveaux processus catalytiques Au(I)/Au(III). (Doctoral Dissertation). Université Toulouse III – Paul Sabatier. Retrieved from http://www.theses.fr/2017TOU30308

Chicago Manual of Style (16th Edition):

Zeineddine, Abdallah. “Harnessing the reactivity of gold via ligand design : stabilization of reactive intermediates and development of new Au(I)/Au(III) catalytic pathways : Exploitation de la réactivité de l'or via le design des ligands : stabilisation des intermédiaires réactionnels et développement de nouveaux processus catalytiques Au(I)/Au(III).” 2017. Doctoral Dissertation, Université Toulouse III – Paul Sabatier. Accessed January 27, 2021. http://www.theses.fr/2017TOU30308.

MLA Handbook (7th Edition):

Zeineddine, Abdallah. “Harnessing the reactivity of gold via ligand design : stabilization of reactive intermediates and development of new Au(I)/Au(III) catalytic pathways : Exploitation de la réactivité de l'or via le design des ligands : stabilisation des intermédiaires réactionnels et développement de nouveaux processus catalytiques Au(I)/Au(III).” 2017. Web. 27 Jan 2021.

Vancouver:

Zeineddine A. Harnessing the reactivity of gold via ligand design : stabilization of reactive intermediates and development of new Au(I)/Au(III) catalytic pathways : Exploitation de la réactivité de l'or via le design des ligands : stabilisation des intermédiaires réactionnels et développement de nouveaux processus catalytiques Au(I)/Au(III). [Internet] [Doctoral dissertation]. Université Toulouse III – Paul Sabatier; 2017. [cited 2021 Jan 27]. Available from: http://www.theses.fr/2017TOU30308.

Council of Science Editors:

Zeineddine A. Harnessing the reactivity of gold via ligand design : stabilization of reactive intermediates and development of new Au(I)/Au(III) catalytic pathways : Exploitation de la réactivité de l'or via le design des ligands : stabilisation des intermédiaires réactionnels et développement de nouveaux processus catalytiques Au(I)/Au(III). [Doctoral Dissertation]. Université Toulouse III – Paul Sabatier; 2017. Available from: http://www.theses.fr/2017TOU30308

16. M. Dell'Acqua. NEW SYNTHETIC STRATEGIES FOR THE PREPARATION OF HETEROCYCLIC AND HETEROPOLYCYCLIC COMPOUNDS.

Degree: 2012, Università degli Studi di Milano

 The aim of the project of this doctoral thesis is the development of new synthetic strategies for the preparation of heterocyclic and heteropolycyclic compounds of… (more)

Subjects/Keywords: alkynes; heterocycles; domino reaction; multicomponent reaction; microwave-promoted synthesis; direct arylation; ammonia; palladium; gold; silver; Settore CHIM/06 - Chimica Organica

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APA (6th Edition):

Dell'Acqua, M. (2012). NEW SYNTHETIC STRATEGIES FOR THE PREPARATION OF HETEROCYCLIC AND HETEROPOLYCYCLIC COMPOUNDS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/170500

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):

Dell'Acqua, M.. “NEW SYNTHETIC STRATEGIES FOR THE PREPARATION OF HETEROCYCLIC AND HETEROPOLYCYCLIC COMPOUNDS.” 2012. Thesis, Università degli Studi di Milano. Accessed January 27, 2021. http://hdl.handle.net/2434/170500.

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

MLA Handbook (7th Edition):

Dell'Acqua, M.. “NEW SYNTHETIC STRATEGIES FOR THE PREPARATION OF HETEROCYCLIC AND HETEROPOLYCYCLIC COMPOUNDS.” 2012. Web. 27 Jan 2021.

Vancouver:

Dell'Acqua M. NEW SYNTHETIC STRATEGIES FOR THE PREPARATION OF HETEROCYCLIC AND HETEROPOLYCYCLIC COMPOUNDS. [Internet] [Thesis]. Università degli Studi di Milano; 2012. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/2434/170500.

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

Council of Science Editors:

Dell'Acqua M. NEW SYNTHETIC STRATEGIES FOR THE PREPARATION OF HETEROCYCLIC AND HETEROPOLYCYCLIC COMPOUNDS. [Thesis]. Università degli Studi di Milano; 2012. Available from: http://hdl.handle.net/2434/170500

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

17. Grolleau, Jérémie. Synthèse de nouveaux semi-conducteurs organiques par arylation directe : Synthesis of new organic semiconducteurs by direct arylation.

Degree: Docteur es, Chimie, 2016, Angers

Les recherches sur le photovoltaïque organique depuis une dizaine d’année ont permis une constante progression de l’efficacité des cellules solaires. Plusieurs groupes de recherche ont… (more)

Subjects/Keywords: Emission induite par agrégation; Organic semiconducteur; Organic photovoltaics; Direct arylation; Substitued thiophene; Aggregation-Induced emission; Benzofuran; 540

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APA (6th Edition):

Grolleau, J. (2016). Synthèse de nouveaux semi-conducteurs organiques par arylation directe : Synthesis of new organic semiconducteurs by direct arylation. (Doctoral Dissertation). Angers. Retrieved from http://www.theses.fr/2016ANGE0029

Chicago Manual of Style (16th Edition):

Grolleau, Jérémie. “Synthèse de nouveaux semi-conducteurs organiques par arylation directe : Synthesis of new organic semiconducteurs by direct arylation.” 2016. Doctoral Dissertation, Angers. Accessed January 27, 2021. http://www.theses.fr/2016ANGE0029.

MLA Handbook (7th Edition):

Grolleau, Jérémie. “Synthèse de nouveaux semi-conducteurs organiques par arylation directe : Synthesis of new organic semiconducteurs by direct arylation.” 2016. Web. 27 Jan 2021.

Vancouver:

Grolleau J. Synthèse de nouveaux semi-conducteurs organiques par arylation directe : Synthesis of new organic semiconducteurs by direct arylation. [Internet] [Doctoral dissertation]. Angers; 2016. [cited 2021 Jan 27]. Available from: http://www.theses.fr/2016ANGE0029.

Council of Science Editors:

Grolleau J. Synthèse de nouveaux semi-conducteurs organiques par arylation directe : Synthesis of new organic semiconducteurs by direct arylation. [Doctoral Dissertation]. Angers; 2016. Available from: http://www.theses.fr/2016ANGE0029


Florida International University

18. Liang, Yong. Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides.

Degree: PhD, Chemistry, 2014, Florida International University

  The antiviral or anticancer activities of C-5 modified pyrimidine nucleoside analogues validate the need for the development of their syntheses. In the first half… (more)

Subjects/Keywords: Nucleoside; Pd-catalyzed Cross-coupling; Palladium; Click Chemistry; Hydrogermylation; C-H activation; Direct Arylation; Organic Chemistry

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APA (6th Edition):

Liang, Y. (2014). Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides. (Doctoral Dissertation). Florida International University. Retrieved from https://digitalcommons.fiu.edu/etd/1591 ; 10.25148/etd.FI14110716 ; FI14110716

Chicago Manual of Style (16th Edition):

Liang, Yong. “Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides.” 2014. Doctoral Dissertation, Florida International University. Accessed January 27, 2021. https://digitalcommons.fiu.edu/etd/1591 ; 10.25148/etd.FI14110716 ; FI14110716.

MLA Handbook (7th Edition):

Liang, Yong. “Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides.” 2014. Web. 27 Jan 2021.

Vancouver:

Liang Y. Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides. [Internet] [Doctoral dissertation]. Florida International University; 2014. [cited 2021 Jan 27]. Available from: https://digitalcommons.fiu.edu/etd/1591 ; 10.25148/etd.FI14110716 ; FI14110716.

Council of Science Editors:

Liang Y. Novel Approaches for the Synthesis of C-5 Modified Pyrimidine Nucleosides. [Doctoral Dissertation]. Florida International University; 2014. Available from: https://digitalcommons.fiu.edu/etd/1591 ; 10.25148/etd.FI14110716 ; FI14110716

19. Tan, Yichen. Palladium-Catalyzed Direct Functionalization of Aromatic C-H Bonds: Development of Methods for Direct Amination and Mechanistic Studies of Direct Arylation of Benzene and Pyridine N-Oxide.

Degree: Chemistry, 2013, University of California – Berkeley

 This dissertation discusses three studies on the Pd-catalyzed direct functionalization of aromatic C-H bonds. 1) Methods for direct amination are developed. 2) Mechanistic studies on… (more)

Subjects/Keywords: Chemistry; C-H Functionalization; Direct Amination; Direct Arylation; Palladium

Direct Arylation of Arenes. Direct functionalization of aromatic C-H bonds offers an attractive… …amination and direct arylation, which are the topics of the research described in this thesis… …of initial intermolecular direct arylation, followed by intramolecular direct amination. 5… …and direct arylation,43 13 sterically controlled amination processes that would make this… …two decades, various methods have been developed for the direct arylation of a variety of… 

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APA (6th Edition):

Tan, Y. (2013). Palladium-Catalyzed Direct Functionalization of Aromatic C-H Bonds: Development of Methods for Direct Amination and Mechanistic Studies of Direct Arylation of Benzene and Pyridine N-Oxide. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/9hz9d488

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):

Tan, Yichen. “Palladium-Catalyzed Direct Functionalization of Aromatic C-H Bonds: Development of Methods for Direct Amination and Mechanistic Studies of Direct Arylation of Benzene and Pyridine N-Oxide.” 2013. Thesis, University of California – Berkeley. Accessed January 27, 2021. http://www.escholarship.org/uc/item/9hz9d488.

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

MLA Handbook (7th Edition):

Tan, Yichen. “Palladium-Catalyzed Direct Functionalization of Aromatic C-H Bonds: Development of Methods for Direct Amination and Mechanistic Studies of Direct Arylation of Benzene and Pyridine N-Oxide.” 2013. Web. 27 Jan 2021.

Vancouver:

Tan Y. Palladium-Catalyzed Direct Functionalization of Aromatic C-H Bonds: Development of Methods for Direct Amination and Mechanistic Studies of Direct Arylation of Benzene and Pyridine N-Oxide. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2021 Jan 27]. Available from: http://www.escholarship.org/uc/item/9hz9d488.

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

Council of Science Editors:

Tan Y. Palladium-Catalyzed Direct Functionalization of Aromatic C-H Bonds: Development of Methods for Direct Amination and Mechanistic Studies of Direct Arylation of Benzene and Pyridine N-Oxide. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/9hz9d488

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


University of Houston

20. Nadres, Enrico 1979-. PALLADIUM-CATALYZED C–H BOND FUNCTIONALIZATION OF HETEROCYCLES AND AMINES.

Degree: PhD, Chemistry, 2012, University of Houston

 Palladium-catalyzed functionalization of C–H bonds is becoming an important synthetic tool that allows the preparation of desired substances in fewer steps and higher yields compared… (more)

Subjects/Keywords: C-H activation; C-H functionalization; Palladium; Catalysis; Arylation; Alkylation; Amination; Heterocycle; Furan; Pyrrole; Aryl chloride; Aryl iodide; Picolinic acid; Picolinamide; Auxiliary-directed; Auxiliary-assisted; Direct functionalization; Direct

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APA (6th Edition):

Nadres, E. 1. (2012). PALLADIUM-CATALYZED C–H BOND FUNCTIONALIZATION OF HETEROCYCLES AND AMINES. (Doctoral Dissertation). University of Houston. Retrieved from http://hdl.handle.net/10657/708

Chicago Manual of Style (16th Edition):

Nadres, Enrico 1979-. “PALLADIUM-CATALYZED C–H BOND FUNCTIONALIZATION OF HETEROCYCLES AND AMINES.” 2012. Doctoral Dissertation, University of Houston. Accessed January 27, 2021. http://hdl.handle.net/10657/708.

MLA Handbook (7th Edition):

Nadres, Enrico 1979-. “PALLADIUM-CATALYZED C–H BOND FUNCTIONALIZATION OF HETEROCYCLES AND AMINES.” 2012. Web. 27 Jan 2021.

Vancouver:

Nadres E1. PALLADIUM-CATALYZED C–H BOND FUNCTIONALIZATION OF HETEROCYCLES AND AMINES. [Internet] [Doctoral dissertation]. University of Houston; 2012. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/10657/708.

Council of Science Editors:

Nadres E1. PALLADIUM-CATALYZED C–H BOND FUNCTIONALIZATION OF HETEROCYCLES AND AMINES. [Doctoral Dissertation]. University of Houston; 2012. Available from: http://hdl.handle.net/10657/708

21. Skhiri, Aymen. Réactivité des chlorures de benzènesulfonyle pour l'accès à des hétéroarènes et alcènes arylés via des réactions pallado-catalysées : Reactivity of benzenesulfonyl chlorides for access to heteroarenes and arylated alkenes via palladium-catalyzed reactions.

Degree: Docteur es, Chimie, 2017, Rennes 1; Université de Sfax (Tunisie)

Au cours de cette thèse, nous nous sommes intéressés à la synthèse d’hétérocycles arylés via l’activation de liaisons sp2 C-H d’hétéroaromatiques et à la synthèse… (more)

Subjects/Keywords: Arylations; Activation de la liaison C-H; Réaction du Heck; Palladium; Catalyse; Chlorures benzènesulfonyle; Alcènes; Arylation direct; Selenophènes; Arylations; C-H bond activation; Heck reaction; Palladium; Catalysis; Benzenesulfonyl chlorides; Alkenes; Direct arylation; Selenophenes

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APA (6th Edition):

Skhiri, A. (2017). Réactivité des chlorures de benzènesulfonyle pour l'accès à des hétéroarènes et alcènes arylés via des réactions pallado-catalysées : Reactivity of benzenesulfonyl chlorides for access to heteroarenes and arylated alkenes via palladium-catalyzed reactions. (Doctoral Dissertation). Rennes 1; Université de Sfax (Tunisie). Retrieved from http://www.theses.fr/2017REN1S080

Chicago Manual of Style (16th Edition):

Skhiri, Aymen. “Réactivité des chlorures de benzènesulfonyle pour l'accès à des hétéroarènes et alcènes arylés via des réactions pallado-catalysées : Reactivity of benzenesulfonyl chlorides for access to heteroarenes and arylated alkenes via palladium-catalyzed reactions.” 2017. Doctoral Dissertation, Rennes 1; Université de Sfax (Tunisie). Accessed January 27, 2021. http://www.theses.fr/2017REN1S080.

MLA Handbook (7th Edition):

Skhiri, Aymen. “Réactivité des chlorures de benzènesulfonyle pour l'accès à des hétéroarènes et alcènes arylés via des réactions pallado-catalysées : Reactivity of benzenesulfonyl chlorides for access to heteroarenes and arylated alkenes via palladium-catalyzed reactions.” 2017. Web. 27 Jan 2021.

Vancouver:

Skhiri A. Réactivité des chlorures de benzènesulfonyle pour l'accès à des hétéroarènes et alcènes arylés via des réactions pallado-catalysées : Reactivity of benzenesulfonyl chlorides for access to heteroarenes and arylated alkenes via palladium-catalyzed reactions. [Internet] [Doctoral dissertation]. Rennes 1; Université de Sfax (Tunisie); 2017. [cited 2021 Jan 27]. Available from: http://www.theses.fr/2017REN1S080.

Council of Science Editors:

Skhiri A. Réactivité des chlorures de benzènesulfonyle pour l'accès à des hétéroarènes et alcènes arylés via des réactions pallado-catalysées : Reactivity of benzenesulfonyl chlorides for access to heteroarenes and arylated alkenes via palladium-catalyzed reactions. [Doctoral Dissertation]. Rennes 1; Université de Sfax (Tunisie); 2017. Available from: http://www.theses.fr/2017REN1S080


Université de Bordeaux I

22. Naturale, Guillaume. Approches radicalaires pour la fonctionnalisation directe de quinones à visée anticancereuse : Direct functionalization of anticancer quinones through radical reactions.

Degree: Docteur es, Chimie organique, 2012, Université de Bordeaux I

Dans le cadre d’un programme de recherche dédié à la découverte de petites molécules à visée anticancéreuse, nous avons envisagé de concevoir des composés originaux… (more)

Subjects/Keywords: Quinones; Chimie Médicinale; Agents Anticancéreux; Réactions Radicalaires; Alkylation Directe; Arylation Directe; Acides Aminés; Sels de Diazonium; Anilines; Quinones; Medicinal Chemistry; Anticancer Agents; Radical Reactions; C-H Direct Alkylation; C-H Direct Arylation; Amino Acids; Diazonium Salts; Anilines

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APA (6th Edition):

Naturale, G. (2012). Approches radicalaires pour la fonctionnalisation directe de quinones à visée anticancereuse : Direct functionalization of anticancer quinones through radical reactions. (Doctoral Dissertation). Université de Bordeaux I. Retrieved from http://www.theses.fr/2012BOR14635

Chicago Manual of Style (16th Edition):

Naturale, Guillaume. “Approches radicalaires pour la fonctionnalisation directe de quinones à visée anticancereuse : Direct functionalization of anticancer quinones through radical reactions.” 2012. Doctoral Dissertation, Université de Bordeaux I. Accessed January 27, 2021. http://www.theses.fr/2012BOR14635.

MLA Handbook (7th Edition):

Naturale, Guillaume. “Approches radicalaires pour la fonctionnalisation directe de quinones à visée anticancereuse : Direct functionalization of anticancer quinones through radical reactions.” 2012. Web. 27 Jan 2021.

Vancouver:

Naturale G. Approches radicalaires pour la fonctionnalisation directe de quinones à visée anticancereuse : Direct functionalization of anticancer quinones through radical reactions. [Internet] [Doctoral dissertation]. Université de Bordeaux I; 2012. [cited 2021 Jan 27]. Available from: http://www.theses.fr/2012BOR14635.

Council of Science Editors:

Naturale G. Approches radicalaires pour la fonctionnalisation directe de quinones à visée anticancereuse : Direct functionalization of anticancer quinones through radical reactions. [Doctoral Dissertation]. Université de Bordeaux I; 2012. Available from: http://www.theses.fr/2012BOR14635

23. Cohen Potier de Courcy, Anita. Synthèse et évaluation antiparasitaire de nouveaux dérivés du thiazole et apparentés : Synthesis and antiparasitic evaluation of new thiazole derivatives and related structures.

Degree: Docteur es, Sciences, 2012, Aix Marseille Université

L'objectif de ce travail consiste en la synthèse et l'évaluation antiparasitaire in vitro de nouveaux dérivés du thiazole et apparentés. Plusieurs stratégies de synthèse visant… (more)

Subjects/Keywords: Thiazole; Plasmodium falciparum; Activité antiproliférative in vitro; Activité antiplasmodiale in vitro; Pharmacomodulation; Kinases plasmodiales; Srn1; Palladium; Couplage de Suzuki-Miyaura; Arylation directe; Thiazole; Plasmodium falciparum; In vitro antiproliferative activity; In vitro antiplasmodial activity; Pharmacomodulation; Plasmodial kinases; Srn1; Palladium; Suzuki-Miyaura cross-coupling; Direct arylation

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APA (6th Edition):

Cohen Potier de Courcy, A. (2012). Synthèse et évaluation antiparasitaire de nouveaux dérivés du thiazole et apparentés : Synthesis and antiparasitic evaluation of new thiazole derivatives and related structures. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2012AIXM5503

Chicago Manual of Style (16th Edition):

Cohen Potier de Courcy, Anita. “Synthèse et évaluation antiparasitaire de nouveaux dérivés du thiazole et apparentés : Synthesis and antiparasitic evaluation of new thiazole derivatives and related structures.” 2012. Doctoral Dissertation, Aix Marseille Université. Accessed January 27, 2021. http://www.theses.fr/2012AIXM5503.

MLA Handbook (7th Edition):

Cohen Potier de Courcy, Anita. “Synthèse et évaluation antiparasitaire de nouveaux dérivés du thiazole et apparentés : Synthesis and antiparasitic evaluation of new thiazole derivatives and related structures.” 2012. Web. 27 Jan 2021.

Vancouver:

Cohen Potier de Courcy A. Synthèse et évaluation antiparasitaire de nouveaux dérivés du thiazole et apparentés : Synthesis and antiparasitic evaluation of new thiazole derivatives and related structures. [Internet] [Doctoral dissertation]. Aix Marseille Université 2012. [cited 2021 Jan 27]. Available from: http://www.theses.fr/2012AIXM5503.

Council of Science Editors:

Cohen Potier de Courcy A. Synthèse et évaluation antiparasitaire de nouveaux dérivés du thiazole et apparentés : Synthesis and antiparasitic evaluation of new thiazole derivatives and related structures. [Doctoral Dissertation]. Aix Marseille Université 2012. Available from: http://www.theses.fr/2012AIXM5503

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

Degree: 2015, University 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). University Utrecht. Retrieved from https://dspace.library.uu.nl/handle/1874/324941 ; URN:NBN:NL:UI:10-1874-324941 ; 1874/324941 ; urn:isbn:9789039364697 ; URN:NBN:NL:UI:10-1874-324941 ; https://dspace.library.uu.nl/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, University Utrecht. Accessed January 27, 2021. https://dspace.library.uu.nl/handle/1874/324941 ; URN:NBN:NL:UI:10-1874-324941 ; 1874/324941 ; urn:isbn:9789039364697 ; URN:NBN:NL:UI:10-1874-324941 ; https://dspace.library.uu.nl/handle/1874/324941.

MLA Handbook (7th Edition):

Huang, Y. “Practical catalytic arylation of C–H bonds by iron/phenanthroline systems.” 2015. Web. 27 Jan 2021.

Vancouver:

Huang Y. Practical catalytic arylation of C–H bonds by iron/phenanthroline systems. [Internet] [Doctoral dissertation]. University Utrecht; 2015. [cited 2021 Jan 27]. Available from: https://dspace.library.uu.nl/handle/1874/324941 ; URN:NBN:NL:UI:10-1874-324941 ; 1874/324941 ; urn:isbn:9789039364697 ; URN:NBN:NL:UI:10-1874-324941 ; https://dspace.library.uu.nl/handle/1874/324941.

Council of Science Editors:

Huang Y. Practical catalytic arylation of C–H bonds by iron/phenanthroline systems. [Doctoral Dissertation]. University Utrecht; 2015. Available from: https://dspace.library.uu.nl/handle/1874/324941 ; URN:NBN:NL:UI:10-1874-324941 ; 1874/324941 ; urn:isbn:9789039364697 ; URN:NBN:NL:UI:10-1874-324941 ; https://dspace.library.uu.nl/handle/1874/324941


Université de Montréal

25. Ladd, Carolyn L. Intramolecular Direct Functionalization of Cyclopropanes via Silver-Mediated, Palladium Catalysis.

Degree: 2014, Université de Montréal

Subjects/Keywords: Palladium; Silver; Direct arylation; Direct functionalization; Cyclopropanes; Catalysis; Benzoazepinones; Spirooxindoles; Argent; Arylation directe; Fonctionnalisation directe; Catalyse; Chemistry - Organic / Chimie organique (UMI : 0490)

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APA (6th Edition):

Ladd, C. L. (2014). Intramolecular Direct Functionalization of Cyclopropanes via Silver-Mediated, Palladium Catalysis. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/10665

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):

Ladd, Carolyn L. “Intramolecular Direct Functionalization of Cyclopropanes via Silver-Mediated, Palladium Catalysis.” 2014. Thesis, Université de Montréal. Accessed January 27, 2021. http://hdl.handle.net/1866/10665.

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

MLA Handbook (7th Edition):

Ladd, Carolyn L. “Intramolecular Direct Functionalization of Cyclopropanes via Silver-Mediated, Palladium Catalysis.” 2014. Web. 27 Jan 2021.

Vancouver:

Ladd CL. Intramolecular Direct Functionalization of Cyclopropanes via Silver-Mediated, Palladium Catalysis. [Internet] [Thesis]. Université de Montréal; 2014. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/1866/10665.

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

Council of Science Editors:

Ladd CL. Intramolecular Direct Functionalization of Cyclopropanes via Silver-Mediated, Palladium Catalysis. [Thesis]. Université de Montréal; 2014. Available from: http://hdl.handle.net/1866/10665

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

26. Grosse, Sandrine. Imidazo[1, 2-b]pyrazoles, imidazo[1, 2-a]imidazoles : synthèse, fonctionnalisation et évaluation biologique : Imidazo[1,2-b]pyrazoles, imidazo[1,2-a]imidazoles : synthesis, functionalisation and biological evaluation.

Degree: Docteur es, Chimie organique, 2013, Université d'Orléans

Les imidazo[1,2-b]pyrazoles tout comme les imidazo[1,2-a]imidazoles sont des entités présentant diverses applications intéressantes notamment dans le domaine pharmacologique. Cependant, malgré ce potentiel, ces structures hétérobicycliques… (more)

Subjects/Keywords: Imidazo[1,2-b]pyrazoles; Imidazo[1,2-a]imidazoles; Imidazo[1,2-a]imidazolin-2-ones; (hétéro)arylation directe; Metallo-catalysées; Régioselectivité; Suzuki-Miyaura; Micro-ondes; Imidazo[1,2-b]pyrazoles; Imidazo[1,2-a]imidazoles; Imidazo[1,2-a]imidazolin-2-ones; Direct (hetero)arylation; Metallo-catalysed reactions; Regioselectivity; Suzuki-Miyaura; Micro-waves

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APA (6th Edition):

Grosse, S. (2013). Imidazo[1, 2-b]pyrazoles, imidazo[1, 2-a]imidazoles : synthèse, fonctionnalisation et évaluation biologique : Imidazo[1,2-b]pyrazoles, imidazo[1,2-a]imidazoles : synthesis, functionalisation and biological evaluation. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2013ORLE2056

Chicago Manual of Style (16th Edition):

Grosse, Sandrine. “Imidazo[1, 2-b]pyrazoles, imidazo[1, 2-a]imidazoles : synthèse, fonctionnalisation et évaluation biologique : Imidazo[1,2-b]pyrazoles, imidazo[1,2-a]imidazoles : synthesis, functionalisation and biological evaluation.” 2013. Doctoral Dissertation, Université d'Orléans. Accessed January 27, 2021. http://www.theses.fr/2013ORLE2056.

MLA Handbook (7th Edition):

Grosse, Sandrine. “Imidazo[1, 2-b]pyrazoles, imidazo[1, 2-a]imidazoles : synthèse, fonctionnalisation et évaluation biologique : Imidazo[1,2-b]pyrazoles, imidazo[1,2-a]imidazoles : synthesis, functionalisation and biological evaluation.” 2013. Web. 27 Jan 2021.

Vancouver:

Grosse S. Imidazo[1, 2-b]pyrazoles, imidazo[1, 2-a]imidazoles : synthèse, fonctionnalisation et évaluation biologique : Imidazo[1,2-b]pyrazoles, imidazo[1,2-a]imidazoles : synthesis, functionalisation and biological evaluation. [Internet] [Doctoral dissertation]. Université d'Orléans; 2013. [cited 2021 Jan 27]. Available from: http://www.theses.fr/2013ORLE2056.

Council of Science Editors:

Grosse S. Imidazo[1, 2-b]pyrazoles, imidazo[1, 2-a]imidazoles : synthèse, fonctionnalisation et évaluation biologique : Imidazo[1,2-b]pyrazoles, imidazo[1,2-a]imidazoles : synthesis, functionalisation and biological evaluation. [Doctoral Dissertation]. Université d'Orléans; 2013. Available from: http://www.theses.fr/2013ORLE2056


Université de Montréal

27. Mousseau, James J. Direct functionalization of heterocyclic and non-heterocyclic arenes.

Degree: 2011, Université de Montréal

Subjects/Keywords: Ylures de N-iminopyridinium; arylation directe; vinylation; catalyse; palladium; cuivre; fer; groupement directeur; N-Iminopyridinium ylides; direct arylation; alkenylation; catalysis; palladium; copper; iron; directing group; Chemistry - Organic / Chimie organique (UMI : 0490)

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

APA (6th Edition):

Mousseau, J. J. (2011). Direct functionalization of heterocyclic and non-heterocyclic arenes. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/4893

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):

Mousseau, James J. “Direct functionalization of heterocyclic and non-heterocyclic arenes.” 2011. Thesis, Université de Montréal. Accessed January 27, 2021. http://hdl.handle.net/1866/4893.

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

MLA Handbook (7th Edition):

Mousseau, James J. “Direct functionalization of heterocyclic and non-heterocyclic arenes.” 2011. Web. 27 Jan 2021.

Vancouver:

Mousseau JJ. Direct functionalization of heterocyclic and non-heterocyclic arenes. [Internet] [Thesis]. Université de Montréal; 2011. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/1866/4893.

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

Council of Science Editors:

Mousseau JJ. Direct functionalization of heterocyclic and non-heterocyclic arenes. [Thesis]. Université de Montréal; 2011. Available from: http://hdl.handle.net/1866/4893

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


Université de Montréal

28. Ladd, Carolyn L. Palladium-Catalyzed intramolecular sp3 C–H functionalization : studies in cyclopropyl and heterocyclic motifs.

Degree: 2018, Université de Montréal

Subjects/Keywords: palladium; arylation; alkenylation; ring-opening; direct functionalization; cyclopropanes; asymmetric catalysis; heterocycles; indolines; tetrahydroisoquinolones; Alcénylation; Fonctionnalisation des liaisons C–H; Catalyse asymétrique; Hétérocycles; Tétrahydroquinolones; Chemistry - Organic / Chimie organique (UMI : 0490)

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

APA (6th Edition):

Ladd, C. L. (2018). Palladium-Catalyzed intramolecular sp3 C–H functionalization : studies in cyclopropyl and heterocyclic motifs. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/20442

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):

Ladd, Carolyn L. “Palladium-Catalyzed intramolecular sp3 C–H functionalization : studies in cyclopropyl and heterocyclic motifs.” 2018. Thesis, Université de Montréal. Accessed January 27, 2021. http://hdl.handle.net/1866/20442.

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

MLA Handbook (7th Edition):

Ladd, Carolyn L. “Palladium-Catalyzed intramolecular sp3 C–H functionalization : studies in cyclopropyl and heterocyclic motifs.” 2018. Web. 27 Jan 2021.

Vancouver:

Ladd CL. Palladium-Catalyzed intramolecular sp3 C–H functionalization : studies in cyclopropyl and heterocyclic motifs. [Internet] [Thesis]. Université de Montréal; 2018. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/1866/20442.

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

Council of Science Editors:

Ladd CL. Palladium-Catalyzed intramolecular sp3 C–H functionalization : studies in cyclopropyl and heterocyclic motifs. [Thesis]. Université de Montréal; 2018. Available from: http://hdl.handle.net/1866/20442

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


Université de Montréal

29. Vallée, Frédéric. Synthèse de motifs biarylés : fonctionnalisation directe catalysée par des métaux de transition d’espèces aromatiques non activées.

Degree: 2010, Université de Montréal

Subjects/Keywords: Insertion C-H; Activation C-H; Catalyseur de fer; Catalyseur de palladium; Synthèse de biphényles; Mécansime radicalaire; Direct arylation; Iron catalysis; C-H bond functionalization; Radical transfer; Biaryls synthesis; Palladium catalysis; Chemistry - Organic / Chimie organique (UMI : 0490)

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APA (6th Edition):

Vallée, F. (2010). Synthèse de motifs biarylés : fonctionnalisation directe catalysée par des métaux de transition d’espèces aromatiques non activées. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/4409

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):

Vallée, Frédéric. “Synthèse de motifs biarylés : fonctionnalisation directe catalysée par des métaux de transition d’espèces aromatiques non activées.” 2010. Thesis, Université de Montréal. Accessed January 27, 2021. http://hdl.handle.net/1866/4409.

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

MLA Handbook (7th Edition):

Vallée, Frédéric. “Synthèse de motifs biarylés : fonctionnalisation directe catalysée par des métaux de transition d’espèces aromatiques non activées.” 2010. Web. 27 Jan 2021.

Vancouver:

Vallée F. Synthèse de motifs biarylés : fonctionnalisation directe catalysée par des métaux de transition d’espèces aromatiques non activées. [Internet] [Thesis]. Université de Montréal; 2010. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/1866/4409.

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

Council of Science Editors:

Vallée F. Synthèse de motifs biarylés : fonctionnalisation directe catalysée par des métaux de transition d’espèces aromatiques non activées. [Thesis]. Université de Montréal; 2010. Available from: http://hdl.handle.net/1866/4409

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

30. Svensson Akusjärvi, Emma. Mechanistic Investigations of the Direct Arylation of Pyridine N-oxides with Bromoarenes and Structure-Reactivity Relationship of Aryl Palladium Complexes in Transmetalations with Organoboron Compounds.

Degree: 2018, Freie Universität Berlin

 Reaktionsgeschwindigkeiten der katalytischen Reaktionen zwischen Pyridin-N-Oxiden und Bromaromaten: Die direkte Arylierung von 4-substituierten Pyridin-N-oxiden mit Bromaromaten ergibt Arylpyridin- N-oxide in Ausbeuten von 70-80%. Jedoch ergeben… (more)

Subjects/Keywords: C–H bond activation; direct arylation; 2,2'-bipyridine; Suzuki-Miyaura reaction; pyridyl palladium complex; pyridine N-oxide; 500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete Wissenschaften

…Synthesis and Reactivity of Aryl Palladium Complexes in the Direct Arylation of Pyridine… …4 1.2.2 Direct arylation of pyridine N-oxides with halobenzenes… …5 1.2.3 Direct arylation of pyridine N-oxides with heteroaryl halides… …7 1.2.4 Previous mechanistic studies on the direct arylation of pyridine N-oxides… …36 2 Synthesis and Reactivity of Aryl Palladium Complexes in the Direct Arylation of… 

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

APA (6th Edition):

Svensson Akusjärvi, E. (2018). Mechanistic Investigations of the Direct Arylation of Pyridine N-oxides with Bromoarenes and Structure-Reactivity Relationship of Aryl Palladium Complexes in Transmetalations with Organoboron Compounds. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-209

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):

Svensson Akusjärvi, Emma. “Mechanistic Investigations of the Direct Arylation of Pyridine N-oxides with Bromoarenes and Structure-Reactivity Relationship of Aryl Palladium Complexes in Transmetalations with Organoboron Compounds.” 2018. Thesis, Freie Universität Berlin. Accessed January 27, 2021. http://dx.doi.org/10.17169/refubium-209.

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

MLA Handbook (7th Edition):

Svensson Akusjärvi, Emma. “Mechanistic Investigations of the Direct Arylation of Pyridine N-oxides with Bromoarenes and Structure-Reactivity Relationship of Aryl Palladium Complexes in Transmetalations with Organoboron Compounds.” 2018. Web. 27 Jan 2021.

Vancouver:

Svensson Akusjärvi E. Mechanistic Investigations of the Direct Arylation of Pyridine N-oxides with Bromoarenes and Structure-Reactivity Relationship of Aryl Palladium Complexes in Transmetalations with Organoboron Compounds. [Internet] [Thesis]. Freie Universität Berlin; 2018. [cited 2021 Jan 27]. Available from: http://dx.doi.org/10.17169/refubium-209.

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

Council of Science Editors:

Svensson Akusjärvi E. Mechanistic Investigations of the Direct Arylation of Pyridine N-oxides with Bromoarenes and Structure-Reactivity Relationship of Aryl Palladium Complexes in Transmetalations with Organoboron Compounds. [Thesis]. Freie Universität Berlin; 2018. Available from: http://dx.doi.org/10.17169/refubium-209

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

.