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You searched for subject:(Hiyama Cross Coupling). Showing records 1 – 6 of 6 total matches.

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University of California – San Diego

1. Lee, SangHyun. Palladium-catalyzed decarbonylative cross-coupling of cinnamic esters with silicon-based nucleophiles/enolates and oxidative decarboxylative cross-coupling of cinnamic acids with enolate precursors.

Degree: Chemistry, 2018, University of California – San Diego

 Transition metal-catalyzed cross-coupling is a powerful methodology to strategically form carbon-carbon or carbon-heteroatom bonds. Advancements in cross-coupling strategies with diverse organometallic nucleophile reagents have been… (more)

Subjects/Keywords: Chemistry; cross-coupling; decarbonylative coupling; decarboxylative coupling; Hiyama-type; oxygenated precursors; radical-mediated coupling

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

APA (6th Edition):

Lee, S. (2018). Palladium-catalyzed decarbonylative cross-coupling of cinnamic esters with silicon-based nucleophiles/enolates and oxidative decarboxylative cross-coupling of cinnamic acids with enolate precursors. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/5s81c8m1

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):

Lee, SangHyun. “Palladium-catalyzed decarbonylative cross-coupling of cinnamic esters with silicon-based nucleophiles/enolates and oxidative decarboxylative cross-coupling of cinnamic acids with enolate precursors.” 2018. Thesis, University of California – San Diego. Accessed August 25, 2019. http://www.escholarship.org/uc/item/5s81c8m1.

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

MLA Handbook (7th Edition):

Lee, SangHyun. “Palladium-catalyzed decarbonylative cross-coupling of cinnamic esters with silicon-based nucleophiles/enolates and oxidative decarboxylative cross-coupling of cinnamic acids with enolate precursors.” 2018. Web. 25 Aug 2019.

Vancouver:

Lee S. Palladium-catalyzed decarbonylative cross-coupling of cinnamic esters with silicon-based nucleophiles/enolates and oxidative decarboxylative cross-coupling of cinnamic acids with enolate precursors. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2019 Aug 25]. Available from: http://www.escholarship.org/uc/item/5s81c8m1.

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

Council of Science Editors:

Lee S. Palladium-catalyzed decarbonylative cross-coupling of cinnamic esters with silicon-based nucleophiles/enolates and oxidative decarboxylative cross-coupling of cinnamic acids with enolate precursors. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/5s81c8m1

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


University of Victoria

2. Dean, Natalie L. Mass spectrometry, mechanisms, and molecular models - combining research in mass spectrometric reaction monitoring and chemical education.

Degree: Department of Chemistry, 2018, University of Victoria

 This thesis combines work in the areas of mass spectrometric reaction monitoring and chemical education. In the first part of this thesis, real-time mechanistic analysis… (more)

Subjects/Keywords: Mass Spectrometry; Chemical Education; VSEPR; Hiyama Cross-Coupling; Fluorophenylsilane; Molecular Geometry

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

APA (6th Edition):

Dean, N. L. (2018). Mass spectrometry, mechanisms, and molecular models - combining research in mass spectrometric reaction monitoring and chemical education. (Masters Thesis). University of Victoria. Retrieved from https://dspace.library.uvic.ca//handle/1828/9383

Chicago Manual of Style (16th Edition):

Dean, Natalie L. “Mass spectrometry, mechanisms, and molecular models - combining research in mass spectrometric reaction monitoring and chemical education.” 2018. Masters Thesis, University of Victoria. Accessed August 25, 2019. https://dspace.library.uvic.ca//handle/1828/9383.

MLA Handbook (7th Edition):

Dean, Natalie L. “Mass spectrometry, mechanisms, and molecular models - combining research in mass spectrometric reaction monitoring and chemical education.” 2018. Web. 25 Aug 2019.

Vancouver:

Dean NL. Mass spectrometry, mechanisms, and molecular models - combining research in mass spectrometric reaction monitoring and chemical education. [Internet] [Masters thesis]. University of Victoria; 2018. [cited 2019 Aug 25]. Available from: https://dspace.library.uvic.ca//handle/1828/9383.

Council of Science Editors:

Dean NL. Mass spectrometry, mechanisms, and molecular models - combining research in mass spectrometric reaction monitoring and chemical education. [Masters Thesis]. University of Victoria; 2018. Available from: https://dspace.library.uvic.ca//handle/1828/9383


University of St. Andrews

3. Milton, Edward J. Pd catalysed C-C & C-O bond formation using bis-(dialkyl/diarylphosphino)ferrocene ligands .

Degree: 2010, University of St. Andrews

 A brief introduction explaining phosphine ligand properties, Pd catalysed cross-coupling reactions; the importance of the steps involved in the catalytic cycle (oxidative addition, transmetalation &… (more)

Subjects/Keywords: Cross-coupling; Palladium; Kumada; Suzuki; Hiyama; Silicon; Nucleophile; Aryl chloride; Aryl-ether; Buchwald; Super-concentrated; Phosphinoferrocenyl ligands; Grignard reagents

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

APA (6th Edition):

Milton, E. J. (2010). Pd catalysed C-C & C-O bond formation using bis-(dialkyl/diarylphosphino)ferrocene ligands . (Thesis). University of St. Andrews. Retrieved from http://hdl.handle.net/10023/1022

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):

Milton, Edward J. “Pd catalysed C-C & C-O bond formation using bis-(dialkyl/diarylphosphino)ferrocene ligands .” 2010. Thesis, University of St. Andrews. Accessed August 25, 2019. http://hdl.handle.net/10023/1022.

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

MLA Handbook (7th Edition):

Milton, Edward J. “Pd catalysed C-C & C-O bond formation using bis-(dialkyl/diarylphosphino)ferrocene ligands .” 2010. Web. 25 Aug 2019.

Vancouver:

Milton EJ. Pd catalysed C-C & C-O bond formation using bis-(dialkyl/diarylphosphino)ferrocene ligands . [Internet] [Thesis]. University of St. Andrews; 2010. [cited 2019 Aug 25]. Available from: http://hdl.handle.net/10023/1022.

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

Council of Science Editors:

Milton EJ. Pd catalysed C-C & C-O bond formation using bis-(dialkyl/diarylphosphino)ferrocene ligands . [Thesis]. University of St. Andrews; 2010. Available from: http://hdl.handle.net/10023/1022

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

4. Chang, Wen-Tau. Investigation of aryldimethylsilanolates in palladium-catalyzed cross-coupling reactions and development of chiral bis-hydrazone ligands for asymmetric aryl-aryl couplings.

Degree: PhD, 0335, 2014, University of Illinois – Urbana-Champaign

 The preparation of biaryls by palladium-catalyzed cross-coupling of aromatic bromides and chlorides with alkali-metal salts (potassium and sodium) of aryl- and heteroarylsilanols has been developed.… (more)

Subjects/Keywords: Cross Coupling; Hiyama Coupling; Biaryl; Silanolate; Transmetalation; Hammett Study; Hydrazone Ligand; Asymmetric Aryl-Aryl Coupling

…1 1 Cross-Coupling Reactions of Aromatic and Heteroaromatic Silanolates with Aromatic… …formation, the transition-metal catalyzed cross-coupling reaction has ascended to a strategy level… …scaled in the GMP facilities at Pfizer-Groton shows that the use of cross-coupling reactions… …catalyzed cross-coupling reactions for the synthesis of biaryls. Various organometallic donors… …judicious choice of catalysts and ligands.18-20 Despite the advances of this cross-coupling… 

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APA (6th Edition):

Chang, W. (2014). Investigation of aryldimethylsilanolates in palladium-catalyzed cross-coupling reactions and development of chiral bis-hydrazone ligands for asymmetric aryl-aryl couplings. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/46779

Chicago Manual of Style (16th Edition):

Chang, Wen-Tau. “Investigation of aryldimethylsilanolates in palladium-catalyzed cross-coupling reactions and development of chiral bis-hydrazone ligands for asymmetric aryl-aryl couplings.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 25, 2019. http://hdl.handle.net/2142/46779.

MLA Handbook (7th Edition):

Chang, Wen-Tau. “Investigation of aryldimethylsilanolates in palladium-catalyzed cross-coupling reactions and development of chiral bis-hydrazone ligands for asymmetric aryl-aryl couplings.” 2014. Web. 25 Aug 2019.

Vancouver:

Chang W. Investigation of aryldimethylsilanolates in palladium-catalyzed cross-coupling reactions and development of chiral bis-hydrazone ligands for asymmetric aryl-aryl couplings. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Aug 25]. Available from: http://hdl.handle.net/2142/46779.

Council of Science Editors:

Chang W. Investigation of aryldimethylsilanolates in palladium-catalyzed cross-coupling reactions and development of chiral bis-hydrazone ligands for asymmetric aryl-aryl couplings. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/46779


Université de Montréal

5. Bonhomme-Beaulieu, Louis-Philippe. Monohalogénocyclopropanations stéréosélectives à l'aide de carbénoïdes de zinc, couplages croisés de cyclopropylsilanols, cyclisations d'iodures d'alkyle catalysées par le nickel .

Degree: 2012, Université de Montréal

 Les cyclopropanes sont des unités qui sont très importantes en raison de leur présence dans de nombreux produits naturels, dans certaines molécules synthétiques ayant une… (more)

Subjects/Keywords: Halogénocyclopropanation stéréosélective; Stereoselective halocyclopropanation; Réaction de Simmons-Smith; Simmons-Smith reaction; Carbénoïdes de zinc; Zinc carbenoids; Synthèse asymétrique; Asymmetric synthesis; Cyclopropylsilanols; Couplage croisé de Hiyama-Denmark; Hiyama-Denmark cross-coupling; Cyclisation d'iodures d'alkyle; Alkyl iodide cyclization; Catalyse au nickel; Nickel catalysis; Substitution d'arènes par voie homolytique; Homolytic aromatic substitution

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

APA (6th Edition):

Bonhomme-Beaulieu, L. (2012). Monohalogénocyclopropanations stéréosélectives à l'aide de carbénoïdes de zinc, couplages croisés de cyclopropylsilanols, cyclisations d'iodures d'alkyle catalysées par le nickel . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/8796

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):

Bonhomme-Beaulieu, Louis-Philippe. “Monohalogénocyclopropanations stéréosélectives à l'aide de carbénoïdes de zinc, couplages croisés de cyclopropylsilanols, cyclisations d'iodures d'alkyle catalysées par le nickel .” 2012. Thesis, Université de Montréal. Accessed August 25, 2019. http://hdl.handle.net/1866/8796.

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

MLA Handbook (7th Edition):

Bonhomme-Beaulieu, Louis-Philippe. “Monohalogénocyclopropanations stéréosélectives à l'aide de carbénoïdes de zinc, couplages croisés de cyclopropylsilanols, cyclisations d'iodures d'alkyle catalysées par le nickel .” 2012. Web. 25 Aug 2019.

Vancouver:

Bonhomme-Beaulieu L. Monohalogénocyclopropanations stéréosélectives à l'aide de carbénoïdes de zinc, couplages croisés de cyclopropylsilanols, cyclisations d'iodures d'alkyle catalysées par le nickel . [Internet] [Thesis]. Université de Montréal; 2012. [cited 2019 Aug 25]. Available from: http://hdl.handle.net/1866/8796.

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

Council of Science Editors:

Bonhomme-Beaulieu L. Monohalogénocyclopropanations stéréosélectives à l'aide de carbénoïdes de zinc, couplages croisés de cyclopropylsilanols, cyclisations d'iodures d'alkyle catalysées par le nickel . [Thesis]. Université de Montréal; 2012. Available from: http://hdl.handle.net/1866/8796

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

6. Carson, Nessa. 1. Reinvestigation of a catalytic, enantioselective alkene dibromination and chlorohydroxylation, 2. Double cross-coupling reactions of siloxaborolates, 3. The enantioselective synthesis of 3-substituted morpholines using computer-guided catalyst design.

Degree: MS, Chemistry, 2016, University of Illinois – Urbana-Champaign

 In Chapter 1, attempts to reproduce eight, putative, enantioselective dibromination and chlorohydroxylation reactions from oft-cited literature studies are described. The reactions were performed with full… (more)

Subjects/Keywords: Chemistry; Siloxaborolates; Silylboranes; Silicon; Boron; Cross-coupling; Hiyama-Denmark; Suzuki; Silanolates; Enantioselective; Dibromination; SnAP; Stannyl amines; Morpholines; Bisoxazolines; Computational; Modeling; Cyclization; Chlorohydroxylation; Chlorohydrins; Olefins; Palladium; Halofunctionalization; Dibromides; Predictive; Catalytic; Copper

…optimization of conditions for the Hiyama-Denmark cross-coupling. It was hypothesized that oxidative… …chlorohydrin products were generated in racemic form. 13 CHAPTER 2 DOUBLE CROSS-COUPLING REACTIONS… …OF SILOXABOROLATES 1. INTRODUCTION Palladium-catalysed cross-coupling is a pillar of… …by Double Cross-Coupling from Siloxaborolate 24 This double, sequential C–C bond formation… …Scheme 13. Double Cross-Coupling Reactions of Other Siloxaborates Additionally, since the… 

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

APA (6th Edition):

Carson, N. (2016). 1. Reinvestigation of a catalytic, enantioselective alkene dibromination and chlorohydroxylation, 2. Double cross-coupling reactions of siloxaborolates, 3. The enantioselective synthesis of 3-substituted morpholines using computer-guided catalyst design. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95419

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):

Carson, Nessa. “1. Reinvestigation of a catalytic, enantioselective alkene dibromination and chlorohydroxylation, 2. Double cross-coupling reactions of siloxaborolates, 3. The enantioselective synthesis of 3-substituted morpholines using computer-guided catalyst design.” 2016. Thesis, University of Illinois – Urbana-Champaign. Accessed August 25, 2019. http://hdl.handle.net/2142/95419.

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

MLA Handbook (7th Edition):

Carson, Nessa. “1. Reinvestigation of a catalytic, enantioselective alkene dibromination and chlorohydroxylation, 2. Double cross-coupling reactions of siloxaborolates, 3. The enantioselective synthesis of 3-substituted morpholines using computer-guided catalyst design.” 2016. Web. 25 Aug 2019.

Vancouver:

Carson N. 1. Reinvestigation of a catalytic, enantioselective alkene dibromination and chlorohydroxylation, 2. Double cross-coupling reactions of siloxaborolates, 3. The enantioselective synthesis of 3-substituted morpholines using computer-guided catalyst design. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Aug 25]. Available from: http://hdl.handle.net/2142/95419.

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

Council of Science Editors:

Carson N. 1. Reinvestigation of a catalytic, enantioselective alkene dibromination and chlorohydroxylation, 2. Double cross-coupling reactions of siloxaborolates, 3. The enantioselective synthesis of 3-substituted morpholines using computer-guided catalyst design. [Thesis]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95419

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

.