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You searched for subject:(Palladium Catalyzed cross Coupling reactions). Showing records 1 – 30 of 18288 total matches.

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University of Illinois – Urbana-Champaign

1. Bailey, Aaron D. Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes.

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

Palladium-catalyzed cross-coupling of ??-substituted allylic silanolates with aryl bromides was investigated. It was discovered that ??-selectivity is heavily influenced by the substituents at silicon. It… (more)

Subjects/Keywords: Palladium-catalyzed cross-coupling reactions; allylic silanes; vinylsilanes

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

APA (6th Edition):

Bailey, A. D. (2011). Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24450

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):

Bailey, Aaron D. “Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes.” 2011. Thesis, University of Illinois – Urbana-Champaign. Accessed January 23, 2021. http://hdl.handle.net/2142/24450.

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

MLA Handbook (7th Edition):

Bailey, Aaron D. “Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes.” 2011. Web. 23 Jan 2021.

Vancouver:

Bailey AD. Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2011. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/2142/24450.

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

Council of Science Editors:

Bailey AD. Palladium catalyzed cross-coupling reactions of allyl- and vinylsilanes. [Thesis]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24450

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

2. 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 23, 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. 23 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 23]. 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


University of Washington

3. Lesniak, Valerie Ann. Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids.

Degree: 2016, University of Washington

 A new method to synthesize substituted homoallylic amines is reported. Homoallylic amines are important structural moieties in natural products and pharmaceutical agents. The reaction couples… (more)

Subjects/Keywords: alkenylboronic acid; aziridine; boronic acid; cross-coupling; homoallylic amine; Palladium-catalyzed; Chemistry; Organic chemistry; chemistry

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APA (6th Edition):

Lesniak, V. A. (2016). Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids. (Thesis). University of Washington. Retrieved from http://hdl.handle.net/1773/37060

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):

Lesniak, Valerie Ann. “Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids.” 2016. Thesis, University of Washington. Accessed January 23, 2021. http://hdl.handle.net/1773/37060.

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

MLA Handbook (7th Edition):

Lesniak, Valerie Ann. “Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids.” 2016. Web. 23 Jan 2021.

Vancouver:

Lesniak VA. Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids. [Internet] [Thesis]. University of Washington; 2016. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1773/37060.

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

Council of Science Editors:

Lesniak VA. Palladium-Catalyzed Cross-Couplings of 2-Alkylaziridines and Alkenylboronic Acids. [Thesis]. University of Washington; 2016. Available from: http://hdl.handle.net/1773/37060

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


University of Pennsylvania

4. McGrew, Genette I. Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes.

Degree: 2011, University of Pennsylvania

 Polyarylmethanes are an extremely valuable molecular scaffold used in fields ranging from materials chemistry to medicinal chemistry. They are found in dyes and semiconductor dopants… (more)

Subjects/Keywords: tricarbonylchromium; palladium-catalyzed; cross-coupling; asymmetric; organolithium; polyarylmethanes; Inorganic Chemistry; Organic Chemistry

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APA (6th Edition):

McGrew, G. I. (2011). Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/964

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):

McGrew, Genette I. “Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes.” 2011. Thesis, University of Pennsylvania. Accessed January 23, 2021. https://repository.upenn.edu/edissertations/964.

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

MLA Handbook (7th Edition):

McGrew, Genette I. “Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes.” 2011. Web. 23 Jan 2021.

Vancouver:

McGrew GI. Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes. [Internet] [Thesis]. University of Pennsylvania; 2011. [cited 2021 Jan 23]. Available from: https://repository.upenn.edu/edissertations/964.

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

Council of Science Editors:

McGrew GI. Activation and Catalytic Bond Forming Reactions at Carbon-Hydrogen Bonds of η6-Tricarbonylchromium-Coordinated Benzylic Arenes. [Thesis]. University of Pennsylvania; 2011. Available from: https://repository.upenn.edu/edissertations/964

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


Universidade Estadual de Campinas

5. Silva, Maria das Graças de Oliveira e, 1987-. Complexos de Pd(0) e de Pd(II) com ligante fosfina derivado de ciclotrifosfazeno : síntese, caracterização e avaliação catalítica em reações de acoplamento C-C: Pd(0) and Pd(II) complexes with phosphine ligand derived from cyclotriphosphazene : synthesis, characterization and application in carbon-carbon cross-coupling reactions.

Degree: 2018, Universidade Estadual de Campinas

 Abstract: In order to synthesize a series of hexachlorocyclotriphosphazene and derivate ligands, further coordination to palladium as chelating ligands and application in catalytic carbon-carbon cross-coupling(more)

Subjects/Keywords: Paládio; Ciclofosfazenos; Reações de acoplamento cruzado; Palladium; Cyclophosphazenes; Cross-coupling reactions

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APA (6th Edition):

Silva, Maria das Graças de Oliveira e, 1. (2018). Complexos de Pd(0) e de Pd(II) com ligante fosfina derivado de ciclotrifosfazeno : síntese, caracterização e avaliação catalítica em reações de acoplamento C-C: Pd(0) and Pd(II) complexes with phosphine ligand derived from cyclotriphosphazene : synthesis, characterization and application in carbon-carbon cross-coupling reactions. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/332642

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

Chicago Manual of Style (16th Edition):

Silva, Maria das Graças de Oliveira e, 1987-. “Complexos de Pd(0) e de Pd(II) com ligante fosfina derivado de ciclotrifosfazeno : síntese, caracterização e avaliação catalítica em reações de acoplamento C-C: Pd(0) and Pd(II) complexes with phosphine ligand derived from cyclotriphosphazene : synthesis, characterization and application in carbon-carbon cross-coupling reactions.” 2018. Thesis, Universidade Estadual de Campinas. Accessed January 23, 2021. http://repositorio.unicamp.br/jspui/handle/REPOSIP/332642.

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

MLA Handbook (7th Edition):

Silva, Maria das Graças de Oliveira e, 1987-. “Complexos de Pd(0) e de Pd(II) com ligante fosfina derivado de ciclotrifosfazeno : síntese, caracterização e avaliação catalítica em reações de acoplamento C-C: Pd(0) and Pd(II) complexes with phosphine ligand derived from cyclotriphosphazene : synthesis, characterization and application in carbon-carbon cross-coupling reactions.” 2018. Web. 23 Jan 2021.

Vancouver:

Silva, Maria das Graças de Oliveira e 1. Complexos de Pd(0) e de Pd(II) com ligante fosfina derivado de ciclotrifosfazeno : síntese, caracterização e avaliação catalítica em reações de acoplamento C-C: Pd(0) and Pd(II) complexes with phosphine ligand derived from cyclotriphosphazene : synthesis, characterization and application in carbon-carbon cross-coupling reactions. [Internet] [Thesis]. Universidade Estadual de Campinas; 2018. [cited 2021 Jan 23]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/332642.

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

Council of Science Editors:

Silva, Maria das Graças de Oliveira e 1. Complexos de Pd(0) e de Pd(II) com ligante fosfina derivado de ciclotrifosfazeno : síntese, caracterização e avaliação catalítica em reações de acoplamento C-C: Pd(0) and Pd(II) complexes with phosphine ligand derived from cyclotriphosphazene : synthesis, characterization and application in carbon-carbon cross-coupling reactions. [Thesis]. Universidade Estadual de Campinas; 2018. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/332642

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

6. Gigant, Nicolas. Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds.

Degree: Docteur es, Chimie organique, 2012, Université d'Orléans

La nécessité grandissante de disposer d’une large librairie de diverses petites molécules pour le screening biologique constitue une puissante force motrice pour les chimistes organiciens… (more)

Subjects/Keywords: Enamide; Diversité moléculaire; Synthèse orientée vers la diversité; Phosphates vinyliques; Additions d’aza-Michaël; Nitrènes; Réactions de couplage pallado-catalysées; Réactions en cascades; Enamides; Molecular diversity; Diversity-oriented synthesis; Vinylphosphates; Aza-Michael additions; Nitrenes; Palladium-catalyzed cross-coupling reactions; Cascade reactions

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APA (6th Edition):

Gigant, N. (2012). Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2012ORLE2039

Chicago Manual of Style (16th Edition):

Gigant, Nicolas. “Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds.” 2012. Doctoral Dissertation, Université d'Orléans. Accessed January 23, 2021. http://www.theses.fr/2012ORLE2039.

MLA Handbook (7th Edition):

Gigant, Nicolas. “Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds.” 2012. Web. 23 Jan 2021.

Vancouver:

Gigant N. Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds. [Internet] [Doctoral dissertation]. Université d'Orléans; 2012. [cited 2021 Jan 23]. Available from: http://www.theses.fr/2012ORLE2039.

Council of Science Editors:

Gigant N. Synthèse et réactivité d'énamides, de la diversité moléculaire à la synthèse de molécules bioactives et/ou naturelles : Synthesis and reactivity of enamides, toward the molecular diversity and the synthesis of bioactive and/or natural compounds. [Doctoral Dissertation]. Université d'Orléans; 2012. Available from: http://www.theses.fr/2012ORLE2039


McMaster University

7. Todorovic, Nikola. DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES.

Degree: PhD, 2012, McMaster University

The development of parallel syntheses that allow for rapid access to compound libraries is widely sought after in drug development and in the study… (more)

Subjects/Keywords: Compound libraries; Isoquinolines; Pyrazolopyrimidines; Toxoflavin; Palladium-catalyzed cross-coupling; Microwave-assisted heating; Organic Chemistry; Organic Chemistry

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APA (6th Edition):

Todorovic, N. (2012). DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/12471

Chicago Manual of Style (16th Edition):

Todorovic, Nikola. “DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES.” 2012. Doctoral Dissertation, McMaster University. Accessed January 23, 2021. http://hdl.handle.net/11375/12471.

MLA Handbook (7th Edition):

Todorovic, Nikola. “DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES.” 2012. Web. 23 Jan 2021.

Vancouver:

Todorovic N. DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES. [Internet] [Doctoral dissertation]. McMaster University; 2012. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/11375/12471.

Council of Science Editors:

Todorovic N. DEVELOPMENT AND APPLICATION OF SYNTHETIC PROTOCOLS FOR THE GENERATION OF HETEROCYCLIC COMPOUND LIBRARIES. [Doctoral Dissertation]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12471


Florida International University

8. Pitteloud, Jean-Philippe. New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues.

Degree: Chemistry, 2010, Florida International University

  The diverse biological properties exhibited by uridine analogues modified at carbon-5 of the uracil base have attracted special interest to the development of efficient… (more)

Subjects/Keywords: ORGANOGERMANES; PALLADIUM-CATALYZED; CROSS-COUPLING; TRANSMETALLATION; URIDINE; NUCLEOSIDES

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APA (6th Edition):

Pitteloud, J. (2010). New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues. (Thesis). Florida International University. Retrieved from https://digitalcommons.fiu.edu/etd/170 ; 10.25148/etd.FI10041621 ; FI10041621

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):

Pitteloud, Jean-Philippe. “New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues.” 2010. Thesis, Florida International University. Accessed January 23, 2021. https://digitalcommons.fiu.edu/etd/170 ; 10.25148/etd.FI10041621 ; FI10041621.

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

MLA Handbook (7th Edition):

Pitteloud, Jean-Philippe. “New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues.” 2010. Web. 23 Jan 2021.

Vancouver:

Pitteloud J. New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues. [Internet] [Thesis]. Florida International University; 2010. [cited 2021 Jan 23]. Available from: https://digitalcommons.fiu.edu/etd/170 ; 10.25148/etd.FI10041621 ; FI10041621.

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

Council of Science Editors:

Pitteloud J. New Organogermanium Substrates for Palladium-Catalyzed Cross-Coupling Reactions. Application of Organogermanes towards the Synthesis of Carbon-5 Modified Uridine Analogues. [Thesis]. Florida International University; 2010. Available from: https://digitalcommons.fiu.edu/etd/170 ; 10.25148/etd.FI10041621 ; FI10041621

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


Florida International University

9. 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 23, 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. 23 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 23]. 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


East Carolina University

10. Harris, Caleb F. Synthesis and Reactions of Novel Heteroarylzirconocene Reagents.

Degree: MS, Chemistry, 2012, East Carolina University

 The cross-coupling of metallated heteroaromatic species with aryl and heteroaryl halides is a powerful and highly desirable transformation in both the synthesis of pharmaceutical compounds… (more)

Subjects/Keywords: Chemistry; Cross-coupling; Heteroaromatic; Organometallic; Palladium-catalyzed; Zirconocene; Zirconium; Chemical tests and reagents; Organic compounds – Synthesis; Halides

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APA (6th Edition):

Harris, C. F. (2012). Synthesis and Reactions of Novel Heteroarylzirconocene Reagents. (Masters Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/4004

Chicago Manual of Style (16th Edition):

Harris, Caleb F. “Synthesis and Reactions of Novel Heteroarylzirconocene Reagents.” 2012. Masters Thesis, East Carolina University. Accessed January 23, 2021. http://hdl.handle.net/10342/4004.

MLA Handbook (7th Edition):

Harris, Caleb F. “Synthesis and Reactions of Novel Heteroarylzirconocene Reagents.” 2012. Web. 23 Jan 2021.

Vancouver:

Harris CF. Synthesis and Reactions of Novel Heteroarylzirconocene Reagents. [Internet] [Masters thesis]. East Carolina University; 2012. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/10342/4004.

Council of Science Editors:

Harris CF. Synthesis and Reactions of Novel Heteroarylzirconocene Reagents. [Masters Thesis]. East Carolina University; 2012. Available from: http://hdl.handle.net/10342/4004

11. Fersing, Cyril. Synthèse et étude des relations structure-activité de nouvelles 3-nitroimidazo (1,2-a) pyridines anti-kinétoplastidés : Synthesis and structure-activity relationships study of new anti-kinetoplastid 3-nitroimidazo[1,2-a]pyridines.

Degree: Docteur es, Sciences Chimiques, 2018, Aix Marseille Université

Les maladies tropicales négligées causées par les protozoaires kinétoplastidés du genre Leishmania et Trypanosoma représentent une menace pour près d’un demi-milliard de personnes en zone… (more)

Subjects/Keywords: Pharmacomodulation anti-Kinétoplastidés; Nitrohétérocycles; Nitroréductases; Couplages pallado-Catalysés; Relations structure-Activité; Leishmania sp; Trypanosoma sp.; Imidazo[1; 2-A]pyridine; Anti-Kinetoplastids pharmacomodulation; Nitroheterocycles; Nitroreductases; Imidazo[1; 2-A]pyridine; Palladium-Catalyzed cross-Coupling reactions; Structure-Activity relationships; Leishmania spp; Trypanosoma spp.; Imidazo[1; 2-A]pyridine

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APA (6th Edition):

Fersing, C. (2018). Synthèse et étude des relations structure-activité de nouvelles 3-nitroimidazo (1,2-a) pyridines anti-kinétoplastidés : Synthesis and structure-activity relationships study of new anti-kinetoplastid 3-nitroimidazo[1,2-a]pyridines. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2018AIXM0275

Chicago Manual of Style (16th Edition):

Fersing, Cyril. “Synthèse et étude des relations structure-activité de nouvelles 3-nitroimidazo (1,2-a) pyridines anti-kinétoplastidés : Synthesis and structure-activity relationships study of new anti-kinetoplastid 3-nitroimidazo[1,2-a]pyridines.” 2018. Doctoral Dissertation, Aix Marseille Université. Accessed January 23, 2021. http://www.theses.fr/2018AIXM0275.

MLA Handbook (7th Edition):

Fersing, Cyril. “Synthèse et étude des relations structure-activité de nouvelles 3-nitroimidazo (1,2-a) pyridines anti-kinétoplastidés : Synthesis and structure-activity relationships study of new anti-kinetoplastid 3-nitroimidazo[1,2-a]pyridines.” 2018. Web. 23 Jan 2021.

Vancouver:

Fersing C. Synthèse et étude des relations structure-activité de nouvelles 3-nitroimidazo (1,2-a) pyridines anti-kinétoplastidés : Synthesis and structure-activity relationships study of new anti-kinetoplastid 3-nitroimidazo[1,2-a]pyridines. [Internet] [Doctoral dissertation]. Aix Marseille Université 2018. [cited 2021 Jan 23]. Available from: http://www.theses.fr/2018AIXM0275.

Council of Science Editors:

Fersing C. Synthèse et étude des relations structure-activité de nouvelles 3-nitroimidazo (1,2-a) pyridines anti-kinétoplastidés : Synthesis and structure-activity relationships study of new anti-kinetoplastid 3-nitroimidazo[1,2-a]pyridines. [Doctoral Dissertation]. Aix Marseille Université 2018. Available from: http://www.theses.fr/2018AIXM0275


University of Edinburgh

12. Clavadetscher, Jessica Veronica. Transition metal catalysis : a new paradigm in bioorthogonal drug activation.

Degree: PhD, 2017, University of Edinburgh

 Powerful tools have emerged in the past few years to allow the sensing, imaging and modulation of biological processes in living systems. Bioorthogonal organometallic reactions(more)

Subjects/Keywords: 547; bioorthogonal reactions; nanoparticle catalysts; zebrafish; bioorthogonal organometallic reactions; palladium-mediated cross-coupling; decaging; copper nanoparticles

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APA (6th Edition):

Clavadetscher, J. V. (2017). Transition metal catalysis : a new paradigm in bioorthogonal drug activation. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/29580

Chicago Manual of Style (16th Edition):

Clavadetscher, Jessica Veronica. “Transition metal catalysis : a new paradigm in bioorthogonal drug activation.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed January 23, 2021. http://hdl.handle.net/1842/29580.

MLA Handbook (7th Edition):

Clavadetscher, Jessica Veronica. “Transition metal catalysis : a new paradigm in bioorthogonal drug activation.” 2017. Web. 23 Jan 2021.

Vancouver:

Clavadetscher JV. Transition metal catalysis : a new paradigm in bioorthogonal drug activation. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1842/29580.

Council of Science Editors:

Clavadetscher JV. Transition metal catalysis : a new paradigm in bioorthogonal drug activation. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/29580


Université Paris-Sud – Paris XI

13. Roche, Maxime. Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4.

Degree: Docteur es, Chimie thérapeutique, 2014, Université Paris-Sud – Paris XI

Les travaux rapportés dans ce mémoire concernent le développement de nouveaux couplages pallado-catalysés de N-tosylhydrazones ainsi que leurs applications à la synthèse d’analogues de l’isocombrétastatine… (more)

Subjects/Keywords: Combrétastatine; Antivasculaire; N-tosylhydrazone; Couplage pallado-catalysé; Réaction tandem; Couplage oxydatif; Combretastatin; Antivascular; N-tosylhydrazone; Palladium catalyzed cross-coupling; Tandem reaction; Oxidative coupling

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APA (6th Edition):

Roche, M. (2014). Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA114843

Chicago Manual of Style (16th Edition):

Roche, Maxime. “Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4.” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed January 23, 2021. http://www.theses.fr/2014PA114843.

MLA Handbook (7th Edition):

Roche, Maxime. “Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4.” 2014. Web. 23 Jan 2021.

Vancouver:

Roche M. Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2021 Jan 23]. Available from: http://www.theses.fr/2014PA114843.

Council of Science Editors:

Roche M. Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA114843


University of Toronto

14. Chai, David. Synthesis of Heterocycles and Carbocycles Through Tandem and Domino Palladium-catalyzed Reactions.

Degree: 2011, University of Toronto

We have described two important classes of palladium-catalyzed reactions for the synthesis of heterocycles and carbocycles: tandem Pd-catalyzed reactions of gem-dibromoolefins and domino Pd-catalyzed reactions(more)

Subjects/Keywords: tandem and domino reactions; palladium catalyzed reactions; 0490

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APA (6th Edition):

Chai, D. (2011). Synthesis of Heterocycles and Carbocycles Through Tandem and Domino Palladium-catalyzed Reactions. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/29678

Chicago Manual of Style (16th Edition):

Chai, David. “Synthesis of Heterocycles and Carbocycles Through Tandem and Domino Palladium-catalyzed Reactions.” 2011. Doctoral Dissertation, University of Toronto. Accessed January 23, 2021. http://hdl.handle.net/1807/29678.

MLA Handbook (7th Edition):

Chai, David. “Synthesis of Heterocycles and Carbocycles Through Tandem and Domino Palladium-catalyzed Reactions.” 2011. Web. 23 Jan 2021.

Vancouver:

Chai D. Synthesis of Heterocycles and Carbocycles Through Tandem and Domino Palladium-catalyzed Reactions. [Internet] [Doctoral dissertation]. University of Toronto; 2011. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1807/29678.

Council of Science Editors:

Chai D. Synthesis of Heterocycles and Carbocycles Through Tandem and Domino Palladium-catalyzed Reactions. [Doctoral Dissertation]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/29678

15. Cornelio, Benedetta. Nanoparticules de palladium comme catalyseurs : Conception, analyses et application pour la préparation de dérivés bisaryliques d'intérêt biologique. : Palladium nanoparticles as catalysts : conception, analyses and application for the preparation of bisaryl derivatives of biological interest.

Degree: Docteur es, Pharmacie - STS, 2014, Reims; Université de Chieti-Pescara

Un grand nombre de 3,4-bisindolylmaléimides possède une activité inhibitrice des protéine-kinases. Les 3-isothiazolone-1,(1)-(di)oxydes pouvant être considérées comme des analogues de la maléimide, la fonctionalisation des… (more)

Subjects/Keywords: Nanoparticules de palladium; Nanotubes de carbone; Couplages croisés pallado-Catalysés; Protéine kinase; Anhydrase carbonique; Palladium nanoparticles; Carbon nanotubes; Palladium-Catalysed cross-Coupling reactions; Protein kinase; Carbonic anhydrase; 610

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APA (6th Edition):

Cornelio, B. (2014). Nanoparticules de palladium comme catalyseurs : Conception, analyses et application pour la préparation de dérivés bisaryliques d'intérêt biologique. : Palladium nanoparticles as catalysts : conception, analyses and application for the preparation of bisaryl derivatives of biological interest. (Doctoral Dissertation). Reims; Université de Chieti-Pescara. Retrieved from http://www.theses.fr/2014REIMP203

Chicago Manual of Style (16th Edition):

Cornelio, Benedetta. “Nanoparticules de palladium comme catalyseurs : Conception, analyses et application pour la préparation de dérivés bisaryliques d'intérêt biologique. : Palladium nanoparticles as catalysts : conception, analyses and application for the preparation of bisaryl derivatives of biological interest.” 2014. Doctoral Dissertation, Reims; Université de Chieti-Pescara. Accessed January 23, 2021. http://www.theses.fr/2014REIMP203.

MLA Handbook (7th Edition):

Cornelio, Benedetta. “Nanoparticules de palladium comme catalyseurs : Conception, analyses et application pour la préparation de dérivés bisaryliques d'intérêt biologique. : Palladium nanoparticles as catalysts : conception, analyses and application for the preparation of bisaryl derivatives of biological interest.” 2014. Web. 23 Jan 2021.

Vancouver:

Cornelio B. Nanoparticules de palladium comme catalyseurs : Conception, analyses et application pour la préparation de dérivés bisaryliques d'intérêt biologique. : Palladium nanoparticles as catalysts : conception, analyses and application for the preparation of bisaryl derivatives of biological interest. [Internet] [Doctoral dissertation]. Reims; Université de Chieti-Pescara; 2014. [cited 2021 Jan 23]. Available from: http://www.theses.fr/2014REIMP203.

Council of Science Editors:

Cornelio B. Nanoparticules de palladium comme catalyseurs : Conception, analyses et application pour la préparation de dérivés bisaryliques d'intérêt biologique. : Palladium nanoparticles as catalysts : conception, analyses and application for the preparation of bisaryl derivatives of biological interest. [Doctoral Dissertation]. Reims; Université de Chieti-Pescara; 2014. Available from: http://www.theses.fr/2014REIMP203


NSYSU

16. Chiang, Meng-fan. Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation.

Degree: Master, Chemistry, 2015, NSYSU

 A direct ortho-aroylation of N-arylpyridin-2-amines with aldehydes to afford mono- and di-aroylated N-arylpyridin-2-amines in modest to good yields is presented. In the reaction, palladium(II) acetate,… (more)

Subjects/Keywords: palladium; C-C coupling; C-H activation; catalyzed reaction; ortho-aroylation

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APA (6th Edition):

Chiang, M. (2015). Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604115-140952

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):

Chiang, Meng-fan. “Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation.” 2015. Thesis, NSYSU. Accessed January 23, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604115-140952.

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

MLA Handbook (7th Edition):

Chiang, Meng-fan. “Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation.” 2015. Web. 23 Jan 2021.

Vancouver:

Chiang M. Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation. [Internet] [Thesis]. NSYSU; 2015. [cited 2021 Jan 23]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604115-140952.

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

Council of Science Editors:

Chiang M. Palladium-Catalyzed Direct Ortho-Aroylation of N-Arylpyridin-2-amines with Aldehydes via C-H Activation. [Thesis]. NSYSU; 2015. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0604115-140952

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


NSYSU

17. Chen, Jiun-hong. Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one.

Degree: Master, Chemistry, 2016, NSYSU

 A direct ortho-Arylation of 1-methyl-N-phenyl-1H-indole-3-carboxamide via Carbon-Hydride Bond Activation. In the reaction, Palladium(II) trifluoroacetate, Copper(II) acetate, Potassium phosphate, Pivalic acid, and DMF:1,4-Dioxane=1/9 were used as… (more)

Subjects/Keywords: palladium; ortho-aroylation; C-C coupling; catalyzed reaction; C-H activation

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APA (6th Edition):

Chen, J. (2016). Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618116-111826

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):

Chen, Jiun-hong. “Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one.” 2016. Thesis, NSYSU. Accessed January 23, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618116-111826.

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

MLA Handbook (7th Edition):

Chen, Jiun-hong. “Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one.” 2016. Web. 23 Jan 2021.

Vancouver:

Chen J. Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one. [Internet] [Thesis]. NSYSU; 2016. [cited 2021 Jan 23]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618116-111826.

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

Council of Science Editors:

Chen J. Palladium-Catalyzed Direct Carbon-Hydrogen Activation Reaction to 1-methyl-N-phenyl-1H-indole-3-carboxamide to 11-methyl-5H-indolo[3,2-c]quinolin-6(11H)-one. [Thesis]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618116-111826

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

18. LeBlond, Carl. Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction.

Degree: PhD, Chemistry, 2011, Seton Hall University

Subjects/Keywords: Cross coupling; palladium catalyzed; pallium on carbon; Chemistry; Organic Chemistry

…PdIC Catalyzed Suzuki Cross-Coupling with Aryl Bromides… …69 PdIC Catalyzed Suzuki Cross-Coupling with Aryl Chlorides… …41 Table 2 . Coupling Reactions Catalyzed by Pd/C… …45 Table 3 . Pd/C catalyzed Suzuki cross-coupling results reported by Buchecker et a1… …of the Suzuki Cross-Coupling Reaction… 

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APA (6th Edition):

LeBlond, C. (2011). Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction. (Doctoral Dissertation). Seton Hall University. Retrieved from https://scholarship.shu.edu/dissertations/1242

Chicago Manual of Style (16th Edition):

LeBlond, Carl. “Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction.” 2011. Doctoral Dissertation, Seton Hall University. Accessed January 23, 2021. https://scholarship.shu.edu/dissertations/1242.

MLA Handbook (7th Edition):

LeBlond, Carl. “Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction.” 2011. Web. 23 Jan 2021.

Vancouver:

LeBlond C. Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction. [Internet] [Doctoral dissertation]. Seton Hall University; 2011. [cited 2021 Jan 23]. Available from: https://scholarship.shu.edu/dissertations/1242.

Council of Science Editors:

LeBlond C. Scope and Mechanistic Studies of the Palladium on Carbon Catalyzed Suzuki Cross Coupling Reaction. [Doctoral Dissertation]. Seton Hall University; 2011. Available from: https://scholarship.shu.edu/dissertations/1242

19. Yamamoto, Yutaro. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究.

Degree: 博士(理学), 2017, Kyoto University / 京都大学

新制・課程博士

甲第20205号

理博第4290号

Subjects/Keywords: palladium; aryl chloride; borylation; hydrodechlorination; cross-coupling reactions

Page 1 Page 2 Page 3

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APA (6th Edition):

Yamamoto, Y. (2017). Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/225430 ; http://dx.doi.org/10.14989/doctor.k20205

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):

Yamamoto, Yutaro. “Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究.” 2017. Thesis, Kyoto University / 京都大学. Accessed January 23, 2021. http://hdl.handle.net/2433/225430 ; http://dx.doi.org/10.14989/doctor.k20205.

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

MLA Handbook (7th Edition):

Yamamoto, Yutaro. “Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究.” 2017. Web. 23 Jan 2021.

Vancouver:

Yamamoto Y. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究. [Internet] [Thesis]. Kyoto University / 京都大学; 2017. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/2433/225430 ; http://dx.doi.org/10.14989/doctor.k20205.

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

Council of Science Editors:

Yamamoto Y. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究. [Thesis]. Kyoto University / 京都大学; 2017. Available from: http://hdl.handle.net/2433/225430 ; http://dx.doi.org/10.14989/doctor.k20205

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


Kyoto University

20. Yamamoto, Yutaro. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents .

Degree: 2017, Kyoto University

Subjects/Keywords: palladium; aryl chloride; borylation; hydrodechlorination; cross-coupling reactions

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APA (6th Edition):

Yamamoto, Y. (2017). Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/225430

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):

Yamamoto, Yutaro. “Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents .” 2017. Thesis, Kyoto University. Accessed January 23, 2021. http://hdl.handle.net/2433/225430.

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

MLA Handbook (7th Edition):

Yamamoto, Yutaro. “Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents .” 2017. Web. 23 Jan 2021.

Vancouver:

Yamamoto Y. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents . [Internet] [Thesis]. Kyoto University; 2017. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/2433/225430.

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

Council of Science Editors:

Yamamoto Y. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents . [Thesis]. Kyoto University; 2017. Available from: http://hdl.handle.net/2433/225430

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


King Abdullah University of Science and Technology

21. Walter, Philipp E. Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol.

Degree: 2012, King Abdullah University of Science and Technology

Cross coupling reactions are a well-established tool in modern organic synthesis and play a crucial role in the synthesis of a high number of organic… (more)

Subjects/Keywords: sonogashira; cross-coupling; water; palladium; green

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APA (6th Edition):

Walter, P. E. (2012). Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol. (Thesis). King Abdullah University of Science and Technology. Retrieved from http://hdl.handle.net/10754/262732

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):

Walter, Philipp E. “Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol.” 2012. Thesis, King Abdullah University of Science and Technology. Accessed January 23, 2021. http://hdl.handle.net/10754/262732.

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

MLA Handbook (7th Edition):

Walter, Philipp E. “Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol.” 2012. Web. 23 Jan 2021.

Vancouver:

Walter PE. Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol. [Internet] [Thesis]. King Abdullah University of Science and Technology; 2012. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/10754/262732.

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

Council of Science Editors:

Walter PE. Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol. [Thesis]. King Abdullah University of Science and Technology; 2012. Available from: http://hdl.handle.net/10754/262732

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


Boston College

22. Le, Hai. Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls.

Degree: PhD, Chemistry, 2014, Boston College

 This dissertation details recent developments in palladium catalyzed carbon-carbon bond formation reactions with two areas of focus: the palladium catalyzed branched and enantioselective allyl-allyl cross-coupling,… (more)

Subjects/Keywords: allyl; asymmetric; cross-coupling; organometallic; palladium; synthesis

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

APA (6th Edition):

Le, H. (2014). Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:104389

Chicago Manual of Style (16th Edition):

Le, Hai. “Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls.” 2014. Doctoral Dissertation, Boston College. Accessed January 23, 2021. http://dlib.bc.edu/islandora/object/bc-ir:104389.

MLA Handbook (7th Edition):

Le, Hai. “Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls.” 2014. Web. 23 Jan 2021.

Vancouver:

Le H. Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls. [Internet] [Doctoral dissertation]. Boston College; 2014. [cited 2021 Jan 23]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104389.

Council of Science Editors:

Le H. Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls. [Doctoral Dissertation]. Boston College; 2014. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104389


Boston College

23. Edelstein, Emma Kate. Enantioselective synthesis and stereospecific transformations of organoboronic esters.

Degree: PhD, Chemistry, 2018, Boston College

 This dissertation details the development of several enantioselective or stereospecific transformations involving organoboronic esters. Chapter one will introduce electrophile-induced boronate rearrangements which underpins much of… (more)

Subjects/Keywords: Boron; Catalysis; Cross-Coupling; Enantioselective; Palladium; Stereospecific

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APA (6th Edition):

Edelstein, E. K. (2018). Enantioselective synthesis and stereospecific transformations of organoboronic esters. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:108038

Chicago Manual of Style (16th Edition):

Edelstein, Emma Kate. “Enantioselective synthesis and stereospecific transformations of organoboronic esters.” 2018. Doctoral Dissertation, Boston College. Accessed January 23, 2021. http://dlib.bc.edu/islandora/object/bc-ir:108038.

MLA Handbook (7th Edition):

Edelstein, Emma Kate. “Enantioselective synthesis and stereospecific transformations of organoboronic esters.” 2018. Web. 23 Jan 2021.

Vancouver:

Edelstein EK. Enantioselective synthesis and stereospecific transformations of organoboronic esters. [Internet] [Doctoral dissertation]. Boston College; 2018. [cited 2021 Jan 23]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:108038.

Council of Science Editors:

Edelstein EK. Enantioselective synthesis and stereospecific transformations of organoboronic esters. [Doctoral Dissertation]. Boston College; 2018. Available from: http://dlib.bc.edu/islandora/object/bc-ir:108038


Queens University

24. Fraser, Andrew. Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions .

Degree: Chemistry, 2013, Queens University

 Little attention has been given to the formation of the putative PdL2 species required for Pd-catalyzed cross-coupling reactions. Active species are generally difficult to store… (more)

Subjects/Keywords: Catalysis ; Palladium ; Cross-Coupling ; Organometallic Chemistry

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APA (6th Edition):

Fraser, A. (2013). Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/8094

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):

Fraser, Andrew. “Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions .” 2013. Thesis, Queens University. Accessed January 23, 2021. http://hdl.handle.net/1974/8094.

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

MLA Handbook (7th Edition):

Fraser, Andrew. “Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions .” 2013. Web. 23 Jan 2021.

Vancouver:

Fraser A. Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions . [Internet] [Thesis]. Queens University; 2013. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1974/8094.

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

Council of Science Editors:

Fraser A. Investigations of a New and Improved Precataylst for Palladium Catalyzed Cross Coupling Reactions . [Thesis]. Queens University; 2013. Available from: http://hdl.handle.net/1974/8094

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

25. Kutudila, Pricilia. Structure et réactivité des triarylbismuths : approche théorique et expérimentale : Structure and reactivity of triarylbismuths : theoretical and experimental approach.

Degree: Docteur es, Chimie, 2017, Université Paris-Est

Les triarylbismuths sont des réactifs organométalliques d’un intérêt croissant en synthèse organique, pour leur aptitude à transférer leurs trois groupements aryles dans les réactions de… (more)

Subjects/Keywords: Triarylbismuths; Chimie verte; Calculs DFT; Etude mécanistique; Couplage croisé; Catalyse au Palladium; Triarylbismuths; Green chemistry; DFT calculations; Mechanistic study; Cross-Coupling reactions; Palladium catalysis

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APA (6th Edition):

Kutudila, P. (2017). Structure et réactivité des triarylbismuths : approche théorique et expérimentale : Structure and reactivity of triarylbismuths : theoretical and experimental approach. (Doctoral Dissertation). Université Paris-Est. Retrieved from http://www.theses.fr/2017PESC1123

Chicago Manual of Style (16th Edition):

Kutudila, Pricilia. “Structure et réactivité des triarylbismuths : approche théorique et expérimentale : Structure and reactivity of triarylbismuths : theoretical and experimental approach.” 2017. Doctoral Dissertation, Université Paris-Est. Accessed January 23, 2021. http://www.theses.fr/2017PESC1123.

MLA Handbook (7th Edition):

Kutudila, Pricilia. “Structure et réactivité des triarylbismuths : approche théorique et expérimentale : Structure and reactivity of triarylbismuths : theoretical and experimental approach.” 2017. Web. 23 Jan 2021.

Vancouver:

Kutudila P. Structure et réactivité des triarylbismuths : approche théorique et expérimentale : Structure and reactivity of triarylbismuths : theoretical and experimental approach. [Internet] [Doctoral dissertation]. Université Paris-Est; 2017. [cited 2021 Jan 23]. Available from: http://www.theses.fr/2017PESC1123.

Council of Science Editors:

Kutudila P. Structure et réactivité des triarylbismuths : approche théorique et expérimentale : Structure and reactivity of triarylbismuths : theoretical and experimental approach. [Doctoral Dissertation]. Université Paris-Est; 2017. Available from: http://www.theses.fr/2017PESC1123

26. Da Costa, Laurène. Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections.

Degree: Docteur es, Sciences Chimiques, 2017, Aix Marseille Université

Le rhinovirus (RV) est connu pour être l'étiologie de plus de la moitié des rhumes bénins. Ces virus ont également été associés à des pathologies… (more)

Subjects/Keywords: Rhinovirus; Capsid-Binder; Réaction par transfert monoélectronique; Tdae; Couplages pallado-Catalysés; Méthode de Mosher; Rhinovirus; Capsid-Binder; Single electron transfer (SET) reaction; Tdae; Pallado-Catalyzed cross-Coupling reactions; Mosher’s method

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APA (6th Edition):

Da Costa, L. (2017). Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2017AIXM0350

Chicago Manual of Style (16th Edition):

Da Costa, Laurène. “Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections.” 2017. Doctoral Dissertation, Aix Marseille Université. Accessed January 23, 2021. http://www.theses.fr/2017AIXM0350.

MLA Handbook (7th Edition):

Da Costa, Laurène. “Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections.” 2017. Web. 23 Jan 2021.

Vancouver:

Da Costa L. Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections. [Internet] [Doctoral dissertation]. Aix Marseille Université 2017. [cited 2021 Jan 23]. Available from: http://www.theses.fr/2017AIXM0350.

Council of Science Editors:

Da Costa L. Pharmacochimie de nouveaux inhibiteurs contre les infections à rhinovirus : Pharmacochemistry of new inhibitors against rhinovirus infections. [Doctoral Dissertation]. Aix Marseille Université 2017. Available from: http://www.theses.fr/2017AIXM0350


Université de Bordeaux I

27. Pradhan, Anirban. Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés.

Degree: Docteur es, Chimie, 2013, Université de Bordeaux I

Les nanorubans de carbone présentent aujourd’hui un grand intérêt en tant que segments de graphène aux propriétés électroniques modulables. Alors que des techniques de synthèse… (more)

Subjects/Keywords: Composés aromatiques polycycliques; Nanorubans de carbone; Hélicènes; Réaction de Scholl; Réactions catalysées de couplages croisés; Polycyclic aromatic compounds (PAC); Carbon nanoribbons; Helicenes; Scholl reaction; Catalyzed cross-coupling reactions

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APA (6th Edition):

Pradhan, A. (2013). Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés. (Doctoral Dissertation). Université de Bordeaux I. Retrieved from http://www.theses.fr/2013BOR14849

Chicago Manual of Style (16th Edition):

Pradhan, Anirban. “Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés.” 2013. Doctoral Dissertation, Université de Bordeaux I. Accessed January 23, 2021. http://www.theses.fr/2013BOR14849.

MLA Handbook (7th Edition):

Pradhan, Anirban. “Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés.” 2013. Web. 23 Jan 2021.

Vancouver:

Pradhan A. Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés. [Internet] [Doctoral dissertation]. Université de Bordeaux I; 2013. [cited 2021 Jan 23]. Available from: http://www.theses.fr/2013BOR14849.

Council of Science Editors:

Pradhan A. Distorted arenes by Scholl cyclizations, towards twisted carbon nanoribbons : Synthèse de composés aromatiques polycycliques distordus par réaction de Scholl vers des nanorubans de carbone courbés. [Doctoral Dissertation]. Université de Bordeaux I; 2013. Available from: http://www.theses.fr/2013BOR14849


Boston College

28. Koo, Seung Moh. Preparation of Organoboronates through Nickel-Catalyzed Conjunctive Coupling Reactions and Their Applications.

Degree: MS, Chemistry, 2020, Boston College

 This thesis will describe the development of two transition metal catalyzed syntheses of organoboronic compounds. The first section describes relevant concepts and precedents for the… (more)

Subjects/Keywords: Conjunctive Coupling Reactions; Nickel Catalyzed; Organoboron Compounds; Organoboronates

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APA (6th Edition):

Koo, S. M. (2020). Preparation of Organoboronates through Nickel-Catalyzed Conjunctive Coupling Reactions and Their Applications. (Masters Thesis). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:108956

Chicago Manual of Style (16th Edition):

Koo, Seung Moh. “Preparation of Organoboronates through Nickel-Catalyzed Conjunctive Coupling Reactions and Their Applications.” 2020. Masters Thesis, Boston College. Accessed January 23, 2021. http://dlib.bc.edu/islandora/object/bc-ir:108956.

MLA Handbook (7th Edition):

Koo, Seung Moh. “Preparation of Organoboronates through Nickel-Catalyzed Conjunctive Coupling Reactions and Their Applications.” 2020. Web. 23 Jan 2021.

Vancouver:

Koo SM. Preparation of Organoboronates through Nickel-Catalyzed Conjunctive Coupling Reactions and Their Applications. [Internet] [Masters thesis]. Boston College; 2020. [cited 2021 Jan 23]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:108956.

Council of Science Editors:

Koo SM. Preparation of Organoboronates through Nickel-Catalyzed Conjunctive Coupling Reactions and Their Applications. [Masters Thesis]. Boston College; 2020. Available from: http://dlib.bc.edu/islandora/object/bc-ir:108956


University of Rochester

29. Anka-Lufford, Lukiana L. (1988 - ). Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles.

Degree: PhD, 2016, University of Rochester

 The direct transition-metal catalyzed cross-coupling of two different electrophiles is a fast emerging synthetic method, as it avoids the use of carbon nucleophiles. Despite being… (more)

Subjects/Keywords: Alkyl electrophiles; Aryl halides; Cross-coupling; Nickel-catalyzed

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APA (6th Edition):

Anka-Lufford, L. L. (. -. ). (2016). Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/30406

Chicago Manual of Style (16th Edition):

Anka-Lufford, Lukiana L (1988 - ). “Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles.” 2016. Doctoral Dissertation, University of Rochester. Accessed January 23, 2021. http://hdl.handle.net/1802/30406.

MLA Handbook (7th Edition):

Anka-Lufford, Lukiana L (1988 - ). “Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles.” 2016. Web. 23 Jan 2021.

Vancouver:

Anka-Lufford LL(-). Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles. [Internet] [Doctoral dissertation]. University of Rochester; 2016. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1802/30406.

Council of Science Editors:

Anka-Lufford LL(-). Nickel-catalyzed reductive coupling of aryl halides with alkyl electrophiles. [Doctoral Dissertation]. University of Rochester; 2016. Available from: http://hdl.handle.net/1802/30406

30. 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 January 23, 2021. http://hdl.handle.net/1842/33092.

MLA Handbook (7th Edition):

Geogheghan, Katherine Jayne. “Boronic acid speciation in Suzuki-Miyaura cross-coupling.” 2018. Web. 23 Jan 2021.

Vancouver:

Geogheghan KJ. Boronic acid speciation in Suzuki-Miyaura cross-coupling. [Internet] [Doctoral dissertation]. University of Edinburgh; 2018. [cited 2021 Jan 23]. 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

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