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Dept: Chemistry

You searched for subject:( Coupling). Showing records 1 – 30 of 184 total matches.

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University of California – Irvine

1. Erickson, Lucas William. Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions.

Degree: Chemistry, 2017, University of California – Irvine

 In recent years, the Jarvo lab has developed the field of stereospecific nickel-catalyzed cross-coupling reactions of benzylic electrophiles. This chemistry allows for straightforward synthesis of… (more)

Subjects/Keywords: Chemistry; cross-coupling; cyclopropane; nickel; reductive coupling

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APA (6th Edition):

Erickson, L. W. (2017). Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/3rr443q9

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):

Erickson, Lucas William. “Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions.” 2017. Thesis, University of California – Irvine. Accessed March 23, 2019. http://www.escholarship.org/uc/item/3rr443q9.

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

MLA Handbook (7th Edition):

Erickson, Lucas William. “Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions.” 2017. Web. 23 Mar 2019.

Vancouver:

Erickson LW. Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions. [Internet] [Thesis]. University of California – Irvine; 2017. [cited 2019 Mar 23]. Available from: http://www.escholarship.org/uc/item/3rr443q9.

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

Council of Science Editors:

Erickson LW. Development of Stereospecific Nickel-Catalyzed Cross-Coupling and Reductive Cross-Electrophile Coupling Reactions. [Thesis]. University of California – Irvine; 2017. Available from: http://www.escholarship.org/uc/item/3rr443q9

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


University of California – San Diego

2. 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 (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 March 23, 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. 23 Mar 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 Mar 23]. 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 Illinois – Urbana-Champaign

3. Yousaf, Zain. Development of organosilicon cross-coupling reaction.

Degree: MS, Chemistry, 2015, University of Illinois – Urbana-Champaign

 Use of palladium catalyzed cross-couplings have found widespread use in the pharmaceutical industry and there is a significant ongoing effort to either improve or devise… (more)

Subjects/Keywords: silanolate; cross-coupling

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APA (6th Edition):

Yousaf, Z. (2015). Development of organosilicon cross-coupling reaction. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89275

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):

Yousaf, Zain. “Development of organosilicon cross-coupling reaction.” 2015. Thesis, University of Illinois – Urbana-Champaign. Accessed March 23, 2019. http://hdl.handle.net/2142/89275.

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

MLA Handbook (7th Edition):

Yousaf, Zain. “Development of organosilicon cross-coupling reaction.” 2015. Web. 23 Mar 2019.

Vancouver:

Yousaf Z. Development of organosilicon cross-coupling reaction. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/2142/89275.

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

Council of Science Editors:

Yousaf Z. Development of organosilicon cross-coupling reaction. [Thesis]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89275

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


Queens University

4. Norton, Danielle. A new, improved precatalyst for Suzuki-Miyaura cross-coupling reactions .

Degree: Chemistry, 2009, Queens University

 Carbon-carbon bond formation is one of the most important reactions in organic chemistry, and the Suzuki-Miyaura cross-coupling reaction has become a forerunner in this area.… (more)

Subjects/Keywords: palladium precatalysts; cross-coupling

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APA (6th Edition):

Norton, D. (2009). A new, improved precatalyst for Suzuki-Miyaura cross-coupling reactions . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/1995

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):

Norton, Danielle. “A new, improved precatalyst for Suzuki-Miyaura cross-coupling reactions .” 2009. Thesis, Queens University. Accessed March 23, 2019. http://hdl.handle.net/1974/1995.

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

MLA Handbook (7th Edition):

Norton, Danielle. “A new, improved precatalyst for Suzuki-Miyaura cross-coupling reactions .” 2009. Web. 23 Mar 2019.

Vancouver:

Norton D. A new, improved precatalyst for Suzuki-Miyaura cross-coupling reactions . [Internet] [Thesis]. Queens University; 2009. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/1974/1995.

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

Council of Science Editors:

Norton D. A new, improved precatalyst for Suzuki-Miyaura cross-coupling reactions . [Thesis]. Queens University; 2009. Available from: http://hdl.handle.net/1974/1995

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


University of Texas – Austin

5. -4843-2158. Transition metal-catalyzed redox-triggered C-C couplings of alcohols via transfer hydrogenation.

Degree: Chemistry, 2018, University of Texas – Austin

 In the first chapter, the first example of transfer hydrogenative cross-couplings of styrene with primary alcohols is reported. Using RuHCl(CO)(PCy₃)₂ as the precatalyst, AgOTf or… (more)

Subjects/Keywords: C-C coupling; Transfer hydrogenation

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APA (6th Edition):

-4843-2158. (2018). Transition metal-catalyzed redox-triggered C-C couplings of alcohols via transfer hydrogenation. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63545

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

Chicago Manual of Style (16th Edition):

-4843-2158. “Transition metal-catalyzed redox-triggered C-C couplings of alcohols via transfer hydrogenation.” 2018. Thesis, University of Texas – Austin. Accessed March 23, 2019. http://hdl.handle.net/2152/63545.

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

MLA Handbook (7th Edition):

-4843-2158. “Transition metal-catalyzed redox-triggered C-C couplings of alcohols via transfer hydrogenation.” 2018. Web. 23 Mar 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-4843-2158. Transition metal-catalyzed redox-triggered C-C couplings of alcohols via transfer hydrogenation. [Internet] [Thesis]. University of Texas – Austin; 2018. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/2152/63545.

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

Council of Science Editors:

-4843-2158. Transition metal-catalyzed redox-triggered C-C couplings of alcohols via transfer hydrogenation. [Thesis]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/63545

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

6. Xu, Hongwei. Mechanistic Consideration of C-C Bond Transformations at Cobalt Complexes.

Degree: PhD, Chemistry, 2015, Brown University

 The diamagnetic cobalt(III) dimethyl complex, cis,mer-(PMe3)3Co(CH3)2I, was found to promote selective C-C bond formation affording ethane and triplet (PMe3)3CoI. The mechanism of reductive elimination has… (more)

Subjects/Keywords: C-C bond coupling

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APA (6th Edition):

Xu, H. (2015). Mechanistic Consideration of C-C Bond Transformations at Cobalt Complexes. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:419447/

Chicago Manual of Style (16th Edition):

Xu, Hongwei. “Mechanistic Consideration of C-C Bond Transformations at Cobalt Complexes.” 2015. Doctoral Dissertation, Brown University. Accessed March 23, 2019. https://repository.library.brown.edu/studio/item/bdr:419447/.

MLA Handbook (7th Edition):

Xu, Hongwei. “Mechanistic Consideration of C-C Bond Transformations at Cobalt Complexes.” 2015. Web. 23 Mar 2019.

Vancouver:

Xu H. Mechanistic Consideration of C-C Bond Transformations at Cobalt Complexes. [Internet] [Doctoral dissertation]. Brown University; 2015. [cited 2019 Mar 23]. Available from: https://repository.library.brown.edu/studio/item/bdr:419447/.

Council of Science Editors:

Xu H. Mechanistic Consideration of C-C Bond Transformations at Cobalt Complexes. [Doctoral Dissertation]. Brown University; 2015. Available from: https://repository.library.brown.edu/studio/item/bdr:419447/


Boston College

7. Heusser, Carolyn Andrea. Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement.

Degree: MS, Chemistry, 2013, Boston College

 Chapter 1: There are a limited number of examples of metal-catalyzed Brook rearrangements in the literature, none of which involve ruthenium, rhodium, or iridium which… (more)

Subjects/Keywords: Acylsilane; Brook rearrangement; Cross Coupling

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APA (6th Edition):

Heusser, C. A. (2013). Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement. (Masters Thesis). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101169

Chicago Manual of Style (16th Edition):

Heusser, Carolyn Andrea. “Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement.” 2013. Masters Thesis, Boston College. Accessed March 23, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101169.

MLA Handbook (7th Edition):

Heusser, Carolyn Andrea. “Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement.” 2013. Web. 23 Mar 2019.

Vancouver:

Heusser CA. Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement. [Internet] [Masters thesis]. Boston College; 2013. [cited 2019 Mar 23]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101169.

Council of Science Editors:

Heusser CA. Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement. [Masters Thesis]. Boston College; 2013. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101169


Boston College

8. Kyne, Robert E. Strategic Applications of Pinacolato Allylboron Reagents: New Reactions in Enantioselective Allyl-Allyl Cross-Coupling and Allylboration to Form New Carbon-Heteroatom Bonds.

Degree: PhD, Chemistry, 2012, Boston College

 Detailed within this dissertation are three new reactions involving allylboron reagents. Chapter 1 describes the development of Pd-catalyzed allyl-allyl cross-coupling for the preparation of enantioenriched… (more)

Subjects/Keywords: Allylation; Allylboron; Cross-Coupling; Nitrosobenzene

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APA (6th Edition):

Kyne, R. E. (2012). Strategic Applications of Pinacolato Allylboron Reagents: New Reactions in Enantioselective Allyl-Allyl Cross-Coupling and Allylboration to Form New Carbon-Heteroatom Bonds. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101156

Chicago Manual of Style (16th Edition):

Kyne, Robert E. “Strategic Applications of Pinacolato Allylboron Reagents: New Reactions in Enantioselective Allyl-Allyl Cross-Coupling and Allylboration to Form New Carbon-Heteroatom Bonds.” 2012. Doctoral Dissertation, Boston College. Accessed March 23, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101156.

MLA Handbook (7th Edition):

Kyne, Robert E. “Strategic Applications of Pinacolato Allylboron Reagents: New Reactions in Enantioselective Allyl-Allyl Cross-Coupling and Allylboration to Form New Carbon-Heteroatom Bonds.” 2012. Web. 23 Mar 2019.

Vancouver:

Kyne RE. Strategic Applications of Pinacolato Allylboron Reagents: New Reactions in Enantioselective Allyl-Allyl Cross-Coupling and Allylboration to Form New Carbon-Heteroatom Bonds. [Internet] [Doctoral dissertation]. Boston College; 2012. [cited 2019 Mar 23]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101156.

Council of Science Editors:

Kyne RE. Strategic Applications of Pinacolato Allylboron Reagents: New Reactions in Enantioselective Allyl-Allyl Cross-Coupling and Allylboration to Form New Carbon-Heteroatom Bonds. [Doctoral Dissertation]. Boston College; 2012. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101156


Boston College

9. Schuster, Christopher Henry. Synthesis and Utility of Organoboron Reagents for Enantioselective Synthesis.

Degree: PhD, Chemistry, 2014, Boston College

 Described herein are three distinct projects centered on the formation and use of carbon-boron bonds. In the first, the enantioselective platinum-catalyzed 1,4-diboration of trans-1,3-dienes is… (more)

Subjects/Keywords: cross-coupling; diboration; ligand-development

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APA (6th Edition):

Schuster, C. H. (2014). Synthesis and Utility of Organoboron Reagents for Enantioselective Synthesis. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:103558

Chicago Manual of Style (16th Edition):

Schuster, Christopher Henry. “Synthesis and Utility of Organoboron Reagents for Enantioselective Synthesis.” 2014. Doctoral Dissertation, Boston College. Accessed March 23, 2019. http://dlib.bc.edu/islandora/object/bc-ir:103558.

MLA Handbook (7th Edition):

Schuster, Christopher Henry. “Synthesis and Utility of Organoboron Reagents for Enantioselective Synthesis.” 2014. Web. 23 Mar 2019.

Vancouver:

Schuster CH. Synthesis and Utility of Organoboron Reagents for Enantioselective Synthesis. [Internet] [Doctoral dissertation]. Boston College; 2014. [cited 2019 Mar 23]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:103558.

Council of Science Editors:

Schuster CH. Synthesis and Utility of Organoboron Reagents for Enantioselective Synthesis. [Doctoral Dissertation]. Boston College; 2014. Available from: http://dlib.bc.edu/islandora/object/bc-ir:103558


University of Illinois – Urbana-Champaign

10. Schmidt, Michael Joseph. Design of a second generation MIDA boronate: iterating c(sp3) based Suzuki cross couplings.

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

 Small molecules have had a tremendous positive impact on human health and society in general. Despite this, small molecule synthesis is still a time and… (more)

Subjects/Keywords: Suzuki; coupling; cross coupling; MIDA boronate; iteration; automation

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APA (6th Edition):

Schmidt, M. J. (2016). Design of a second generation MIDA boronate: iterating c(sp3) based Suzuki cross couplings. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95599

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):

Schmidt, Michael Joseph. “Design of a second generation MIDA boronate: iterating c(sp3) based Suzuki cross couplings.” 2016. Thesis, University of Illinois – Urbana-Champaign. Accessed March 23, 2019. http://hdl.handle.net/2142/95599.

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

MLA Handbook (7th Edition):

Schmidt, Michael Joseph. “Design of a second generation MIDA boronate: iterating c(sp3) based Suzuki cross couplings.” 2016. Web. 23 Mar 2019.

Vancouver:

Schmidt MJ. Design of a second generation MIDA boronate: iterating c(sp3) based Suzuki cross couplings. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/2142/95599.

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

Council of Science Editors:

Schmidt MJ. Design of a second generation MIDA boronate: iterating c(sp3) based Suzuki cross couplings. [Thesis]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95599

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


University of Illinois – Urbana-Champaign

11. Gillis, Eric P. Iterative cross-coupling with MIDA boronates.

Degree: PhD, Chemistry, 2010, University of Illinois – Urbana-Champaign

 Many small molecules targeted for synthesis in the laboratory are inherently modular in their construction. Harnessing this modularity towards a unified strategy for the synthesis… (more)

Subjects/Keywords: MIDA; N-methyliminodiacetic acid; iterative cross-coupling; slow-release; MIDA boronate; boronate; cross-coupling; Suzuki cross-coupling

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APA (6th Edition):

Gillis, E. P. (2010). Iterative cross-coupling with MIDA boronates. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/91591

Chicago Manual of Style (16th Edition):

Gillis, Eric P. “Iterative cross-coupling with MIDA boronates.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed March 23, 2019. http://hdl.handle.net/2142/91591.

MLA Handbook (7th Edition):

Gillis, Eric P. “Iterative cross-coupling with MIDA boronates.” 2010. Web. 23 Mar 2019.

Vancouver:

Gillis EP. Iterative cross-coupling with MIDA boronates. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/2142/91591.

Council of Science Editors:

Gillis EP. Iterative cross-coupling with MIDA boronates. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/91591

12. Huddleston, Noah Eric. Metal-mediated interfacial cross coupling reactions: the development of new strategies and catalysts for the preparation of conjugated polymer films.

Degree: PhD, Chemistry, 2013, University of Georgia

 In this dissertation, the surface-initiated polymerization of conjugated polymers using Kumada-catalyst transfer polycondensation (KCTP) combined with new catalysts is presented. Covalently immobilized films of poly(3-methylthiophene)… (more)

Subjects/Keywords: Kumada coupling

…Strategies Towards the Synthesis of Conjugated Polymers .........................4 Kumada Coupling… …Coupling Reaction… …3 Table 4.1: Stille coupling of hindered and unhindered substrates… …105 Table 4.2: Stille coupling of substrates containing various electron donating and… …107 Table 4.3: General intramolecular Stille coupling of substrates with differing halogen… 

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APA (6th Edition):

Huddleston, N. E. (2013). Metal-mediated interfacial cross coupling reactions: the development of new strategies and catalysts for the preparation of conjugated polymer films. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/huddleston_noah_e_201308_phd

Chicago Manual of Style (16th Edition):

Huddleston, Noah Eric. “Metal-mediated interfacial cross coupling reactions: the development of new strategies and catalysts for the preparation of conjugated polymer films.” 2013. Doctoral Dissertation, University of Georgia. Accessed March 23, 2019. http://purl.galileo.usg.edu/uga_etd/huddleston_noah_e_201308_phd.

MLA Handbook (7th Edition):

Huddleston, Noah Eric. “Metal-mediated interfacial cross coupling reactions: the development of new strategies and catalysts for the preparation of conjugated polymer films.” 2013. Web. 23 Mar 2019.

Vancouver:

Huddleston NE. Metal-mediated interfacial cross coupling reactions: the development of new strategies and catalysts for the preparation of conjugated polymer films. [Internet] [Doctoral dissertation]. University of Georgia; 2013. [cited 2019 Mar 23]. Available from: http://purl.galileo.usg.edu/uga_etd/huddleston_noah_e_201308_phd.

Council of Science Editors:

Huddleston NE. Metal-mediated interfacial cross coupling reactions: the development of new strategies and catalysts for the preparation of conjugated polymer films. [Doctoral Dissertation]. University of Georgia; 2013. Available from: http://purl.galileo.usg.edu/uga_etd/huddleston_noah_e_201308_phd


NSYSU

13. Kuo, Chun-Ting. Syntheses, Structure, and Electrochemical Properties of Homo-Metallic Binuclear Complexes Containing [(η5-C5(CH3)5(dppe)M] (M = Fe, Ru and Os) Metal Centers.

Degree: Master, Chemistry, 2009, NSYSU

 Structural determinations and electrochemical properties in the series of multinuclear ferrocenyl-ethynyl complexes with formula [(η5-C5(CH3)5)(P2)MII-Câ¡C-(fc)n-Câ¡C-MII(P2)(η5-C5(CH3)5)] (fc = ferrocenyl; M = Fe(II), Ru(II), Os(II); R =… (more)

Subjects/Keywords: electronic coupling; electrochemical; spacer; ethynyl; ferrocene

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APA (6th Edition):

Kuo, C. (2009). Syntheses, Structure, and Electrochemical Properties of Homo-Metallic Binuclear Complexes Containing [(η5-C5(CH3)5(dppe)M] (M = Fe, Ru and Os) Metal Centers. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0817109-103935

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):

Kuo, Chun-Ting. “Syntheses, Structure, and Electrochemical Properties of Homo-Metallic Binuclear Complexes Containing [(η5-C5(CH3)5(dppe)M] (M = Fe, Ru and Os) Metal Centers.” 2009. Thesis, NSYSU. Accessed March 23, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0817109-103935.

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

MLA Handbook (7th Edition):

Kuo, Chun-Ting. “Syntheses, Structure, and Electrochemical Properties of Homo-Metallic Binuclear Complexes Containing [(η5-C5(CH3)5(dppe)M] (M = Fe, Ru and Os) Metal Centers.” 2009. Web. 23 Mar 2019.

Vancouver:

Kuo C. Syntheses, Structure, and Electrochemical Properties of Homo-Metallic Binuclear Complexes Containing [(η5-C5(CH3)5(dppe)M] (M = Fe, Ru and Os) Metal Centers. [Internet] [Thesis]. NSYSU; 2009. [cited 2019 Mar 23]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0817109-103935.

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

Council of Science Editors:

Kuo C. Syntheses, Structure, and Electrochemical Properties of Homo-Metallic Binuclear Complexes Containing [(η5-C5(CH3)5(dppe)M] (M = Fe, Ru and Os) Metal Centers. [Thesis]. NSYSU; 2009. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0817109-103935

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


Missouri University of Science and Technology

14. Wang, Xiaojiang. Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials.

Degree: M.S. in Chemistry, Chemistry, Missouri University of Science and Technology

 "Immobilization of catalysts is a promising approach to combine the advantages of heterogeneous and homogeneous catalysts. Pd(PPh₃)₂Cl₂ known as an extremely active homogeneous catalyst for… (more)

Subjects/Keywords: Sonogashira coupling; Chemistry

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APA (6th Edition):

Wang, X. (n.d.). Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials. (Masters Thesis). Missouri University of Science and Technology. Retrieved from http://scholarsmine.mst.edu/masters_theses/5905

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

Chicago Manual of Style (16th Edition):

Wang, Xiaojiang. “Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials.” Masters Thesis, Missouri University of Science and Technology. Accessed March 23, 2019. http://scholarsmine.mst.edu/masters_theses/5905.

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

MLA Handbook (7th Edition):

Wang, Xiaojiang. “Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials.” Web. 23 Mar 2019.

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

Vancouver:

Wang X. Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials. [Internet] [Masters thesis]. Missouri University of Science and Technology; [cited 2019 Mar 23]. Available from: http://scholarsmine.mst.edu/masters_theses/5905.

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

Council of Science Editors:

Wang X. Functionalization of mesoporous silicas as powders for support and immobilization of Pd catalysts and as monolithic framework for building strong lightweight materials. [Masters Thesis]. Missouri University of Science and Technology; Available from: http://scholarsmine.mst.edu/masters_theses/5905

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


Queens University

15. Laberge, Veronique. Investigations of Novel Uses for Boron Compounds in Organic and Inorganic Chemistry .

Degree: Chemistry, 2011, Queens University

 Herein I describe a model study to determine the feasibility of organic hydride donors as a source of hydride in the regeneration of ammonia borane.… (more)

Subjects/Keywords: Cross-Coupling; Regeneration of Ammonia Borane

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APA (6th Edition):

Laberge, V. (2011). Investigations of Novel Uses for Boron Compounds in Organic and Inorganic Chemistry . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/6810

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):

Laberge, Veronique. “Investigations of Novel Uses for Boron Compounds in Organic and Inorganic Chemistry .” 2011. Thesis, Queens University. Accessed March 23, 2019. http://hdl.handle.net/1974/6810.

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

MLA Handbook (7th Edition):

Laberge, Veronique. “Investigations of Novel Uses for Boron Compounds in Organic and Inorganic Chemistry .” 2011. Web. 23 Mar 2019.

Vancouver:

Laberge V. Investigations of Novel Uses for Boron Compounds in Organic and Inorganic Chemistry . [Internet] [Thesis]. Queens University; 2011. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/1974/6810.

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

Council of Science Editors:

Laberge V. Investigations of Novel Uses for Boron Compounds in Organic and Inorganic Chemistry . [Thesis]. Queens University; 2011. Available from: http://hdl.handle.net/1974/6810

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


Queens University

16. LaBine, Emily. Enantiospecific, Regioselective Suzuki-Miyaura Cross-Couplings of Secondary, Allylic Boronic Esters .

Degree: Chemistry, 2013, Queens University

 The stereochemical course of the Pd–catalyzed Suzuki-Miyaura cross-coupling of α-substituted, enantioenriched allylic boronic esters with phenyl iodide has been examined. The secondary boronic esters were… (more)

Subjects/Keywords: Suzuki-Miyaura; Regioselective; Catalysis; Enantiospecific; Cross-Coupling

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APA (6th Edition):

LaBine, E. (2013). Enantiospecific, Regioselective Suzuki-Miyaura Cross-Couplings of Secondary, Allylic Boronic Esters . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/8463

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):

LaBine, Emily. “Enantiospecific, Regioselective Suzuki-Miyaura Cross-Couplings of Secondary, Allylic Boronic Esters .” 2013. Thesis, Queens University. Accessed March 23, 2019. http://hdl.handle.net/1974/8463.

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

MLA Handbook (7th Edition):

LaBine, Emily. “Enantiospecific, Regioselective Suzuki-Miyaura Cross-Couplings of Secondary, Allylic Boronic Esters .” 2013. Web. 23 Mar 2019.

Vancouver:

LaBine E. Enantiospecific, Regioselective Suzuki-Miyaura Cross-Couplings of Secondary, Allylic Boronic Esters . [Internet] [Thesis]. Queens University; 2013. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/1974/8463.

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

Council of Science Editors:

LaBine E. Enantiospecific, Regioselective Suzuki-Miyaura Cross-Couplings of Secondary, Allylic Boronic Esters . [Thesis]. Queens University; 2013. Available from: http://hdl.handle.net/1974/8463

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


University of California – Irvine

17. Hanna, Luke Edward. Nickel-Catalyzed Cross-Coupling Reactions: Stereospecific Arylations, Formation of 2-PyridylZinc Reagents & Directed Hydroarylation of Alkynes.

Degree: Chemistry, 2016, University of California – Irvine

 Cross-coupling technology has become an indispensable tool for the rapid and efficient synthesis of complex molecules. Over the past few decades a foundational understanding of… (more)

Subjects/Keywords: Chemistry; Catalysis; Cross-Coupling; Nickel; Organic

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APA (6th Edition):

Hanna, L. E. (2016). Nickel-Catalyzed Cross-Coupling Reactions: Stereospecific Arylations, Formation of 2-PyridylZinc Reagents & Directed Hydroarylation of Alkynes. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/83p514vc

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):

Hanna, Luke Edward. “Nickel-Catalyzed Cross-Coupling Reactions: Stereospecific Arylations, Formation of 2-PyridylZinc Reagents & Directed Hydroarylation of Alkynes.” 2016. Thesis, University of California – Irvine. Accessed March 23, 2019. http://www.escholarship.org/uc/item/83p514vc.

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

MLA Handbook (7th Edition):

Hanna, Luke Edward. “Nickel-Catalyzed Cross-Coupling Reactions: Stereospecific Arylations, Formation of 2-PyridylZinc Reagents & Directed Hydroarylation of Alkynes.” 2016. Web. 23 Mar 2019.

Vancouver:

Hanna LE. Nickel-Catalyzed Cross-Coupling Reactions: Stereospecific Arylations, Formation of 2-PyridylZinc Reagents & Directed Hydroarylation of Alkynes. [Internet] [Thesis]. University of California – Irvine; 2016. [cited 2019 Mar 23]. Available from: http://www.escholarship.org/uc/item/83p514vc.

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

Council of Science Editors:

Hanna LE. Nickel-Catalyzed Cross-Coupling Reactions: Stereospecific Arylations, Formation of 2-PyridylZinc Reagents & Directed Hydroarylation of Alkynes. [Thesis]. University of California – Irvine; 2016. Available from: http://www.escholarship.org/uc/item/83p514vc

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

18. Tollefson, Emily Jean. Development of Stereospecific Nickel-Catalyzed Cross-Coupling Reactions.

Degree: Chemistry, 2016, University of California – Irvine

 The development of asymmetric transition-metal-catalyzed reactions has emerged as an important area of research in the past decade. Advances in the field are transforming the… (more)

Subjects/Keywords: Organic chemistry; Catalysis; Cross-Coupling; Nickel; Stereospecific

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APA (6th Edition):

Tollefson, E. J. (2016). Development of Stereospecific Nickel-Catalyzed Cross-Coupling Reactions. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/9qh2x611

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):

Tollefson, Emily Jean. “Development of Stereospecific Nickel-Catalyzed Cross-Coupling Reactions.” 2016. Thesis, University of California – Irvine. Accessed March 23, 2019. http://www.escholarship.org/uc/item/9qh2x611.

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

MLA Handbook (7th Edition):

Tollefson, Emily Jean. “Development of Stereospecific Nickel-Catalyzed Cross-Coupling Reactions.” 2016. Web. 23 Mar 2019.

Vancouver:

Tollefson EJ. Development of Stereospecific Nickel-Catalyzed Cross-Coupling Reactions. [Internet] [Thesis]. University of California – Irvine; 2016. [cited 2019 Mar 23]. Available from: http://www.escholarship.org/uc/item/9qh2x611.

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

Council of Science Editors:

Tollefson EJ. Development of Stereospecific Nickel-Catalyzed Cross-Coupling Reactions. [Thesis]. University of California – Irvine; 2016. Available from: http://www.escholarship.org/uc/item/9qh2x611

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


University of California – Irvine

19. Harris, Michael. Development of Stereospecific Nickel-Catalyzed Transformations of Benzylic Alcohol Derivatives.

Degree: Chemistry, 2015, University of California – Irvine

 Transition metal catalyzed reactions are indispensable tools for the asymmetric construction of carbon–carbon bonds. Traditionally, cross-coupling reactions have relied on the use of aryl, vinyl… (more)

Subjects/Keywords: Organic chemistry; Catalysis; Cross-coupling; Nickel; Stereospecific

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APA (6th Edition):

Harris, M. (2015). Development of Stereospecific Nickel-Catalyzed Transformations of Benzylic Alcohol Derivatives. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/0c12t0wt

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):

Harris, Michael. “Development of Stereospecific Nickel-Catalyzed Transformations of Benzylic Alcohol Derivatives.” 2015. Thesis, University of California – Irvine. Accessed March 23, 2019. http://www.escholarship.org/uc/item/0c12t0wt.

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

MLA Handbook (7th Edition):

Harris, Michael. “Development of Stereospecific Nickel-Catalyzed Transformations of Benzylic Alcohol Derivatives.” 2015. Web. 23 Mar 2019.

Vancouver:

Harris M. Development of Stereospecific Nickel-Catalyzed Transformations of Benzylic Alcohol Derivatives. [Internet] [Thesis]. University of California – Irvine; 2015. [cited 2019 Mar 23]. Available from: http://www.escholarship.org/uc/item/0c12t0wt.

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

Council of Science Editors:

Harris M. Development of Stereospecific Nickel-Catalyzed Transformations of Benzylic Alcohol Derivatives. [Thesis]. University of California – Irvine; 2015. Available from: http://www.escholarship.org/uc/item/0c12t0wt

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


University of Southern California

20. Fomina, Nadezda. Studies of yamamoto and suzuki polymerizations of dibromofluorenes: synthesis and spectroscopy of fluorene macrocycles and copolymers.

Degree: PhD, Chemistry, 2009, University of Southern California

 This dissertation describes the synthesis of macrocyclic polyfluorenes and fluorene copolymers, end-functionalization of polyfluorenes, conformational studies of polyfluorene chains in dilute solution and kinetics of… (more)

Subjects/Keywords: polyfluorenes; 3,6-dibromofluorene; fluorene macrocycle; Yamamoto coupling

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APA (6th Edition):

Fomina, N. (2009). Studies of yamamoto and suzuki polymerizations of dibromofluorenes: synthesis and spectroscopy of fluorene macrocycles and copolymers. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/177047/rec/6165

Chicago Manual of Style (16th Edition):

Fomina, Nadezda. “Studies of yamamoto and suzuki polymerizations of dibromofluorenes: synthesis and spectroscopy of fluorene macrocycles and copolymers.” 2009. Doctoral Dissertation, University of Southern California. Accessed March 23, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/177047/rec/6165.

MLA Handbook (7th Edition):

Fomina, Nadezda. “Studies of yamamoto and suzuki polymerizations of dibromofluorenes: synthesis and spectroscopy of fluorene macrocycles and copolymers.” 2009. Web. 23 Mar 2019.

Vancouver:

Fomina N. Studies of yamamoto and suzuki polymerizations of dibromofluorenes: synthesis and spectroscopy of fluorene macrocycles and copolymers. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Mar 23]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/177047/rec/6165.

Council of Science Editors:

Fomina N. Studies of yamamoto and suzuki polymerizations of dibromofluorenes: synthesis and spectroscopy of fluorene macrocycles and copolymers. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/177047/rec/6165


University of Michigan

21. Baxter, Ryan David. Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes.

Degree: PhD, Chemistry, 2010, University of Michigan

 Many classes of standard organic transformations involve the coupling or cycloaddition of two different π-components to assemble a more functionalized product. Many such processes are… (more)

Subjects/Keywords: Nickel Catalyzed Reductive Coupling; Chemistry; Science

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APA (6th Edition):

Baxter, R. D. (2010). Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/78979

Chicago Manual of Style (16th Edition):

Baxter, Ryan David. “Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes.” 2010. Doctoral Dissertation, University of Michigan. Accessed March 23, 2019. http://hdl.handle.net/2027.42/78979.

MLA Handbook (7th Edition):

Baxter, Ryan David. “Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes.” 2010. Web. 23 Mar 2019.

Vancouver:

Baxter RD. Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes. [Internet] [Doctoral dissertation]. University of Michigan; 2010. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/2027.42/78979.

Council of Science Editors:

Baxter RD. Method Development and Mechanistic Investigation of Nickel-Catalyzed Reductive Coupling Processes. [Doctoral Dissertation]. University of Michigan; 2010. Available from: http://hdl.handle.net/2027.42/78979


Colorado State University

22. Anderson, Ryan Gerald. Selective functionalization of pyridines and diazines via nucleophilic addition to heterocyclic phosphonium salts.

Degree: MS(M.S.), Chemistry, 2019, Colorado State University

 Nitrogen heterocycles, specifically pyridines and pyrimidines, are common motifs found in pharmaceuticals, agrochemicals and materials. Site-selective functionalization of these azines are highly sought after for… (more)

Subjects/Keywords: Kinase Inhibitors; Pyridines; Phosphonium Salts; Heteroatom Coupling

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APA (6th Edition):

Anderson, R. G. (2019). Selective functionalization of pyridines and diazines via nucleophilic addition to heterocyclic phosphonium salts. (Masters Thesis). Colorado State University. Retrieved from http://hdl.handle.net/10217/193102

Chicago Manual of Style (16th Edition):

Anderson, Ryan Gerald. “Selective functionalization of pyridines and diazines via nucleophilic addition to heterocyclic phosphonium salts.” 2019. Masters Thesis, Colorado State University. Accessed March 23, 2019. http://hdl.handle.net/10217/193102.

MLA Handbook (7th Edition):

Anderson, Ryan Gerald. “Selective functionalization of pyridines and diazines via nucleophilic addition to heterocyclic phosphonium salts.” 2019. Web. 23 Mar 2019.

Vancouver:

Anderson RG. Selective functionalization of pyridines and diazines via nucleophilic addition to heterocyclic phosphonium salts. [Internet] [Masters thesis]. Colorado State University; 2019. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/10217/193102.

Council of Science Editors:

Anderson RG. Selective functionalization of pyridines and diazines via nucleophilic addition to heterocyclic phosphonium salts. [Masters Thesis]. Colorado State University; 2019. Available from: http://hdl.handle.net/10217/193102


University of New South Wales

23. Han, Fei. Thermoresponsive Assembly of Plasmonic Nanostructures and their Reversible Tuning of Plasmon Coupling.

Degree: Chemistry, 2017, University of New South Wales

 Gold nanoparticles (AuNPs) incorporated into the stimuli-responsive polymeric matrix play an increasingly important role in the ‘smart’ optical devices. To date, a myriad of methods… (more)

Subjects/Keywords: Plasmon Coupling; Plasmonic nanostructures; Gold nanoparticles

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APA (6th Edition):

Han, F. (2017). Thermoresponsive Assembly of Plasmonic Nanostructures and their Reversible Tuning of Plasmon Coupling. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/58368 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:45859/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Han, Fei. “Thermoresponsive Assembly of Plasmonic Nanostructures and their Reversible Tuning of Plasmon Coupling.” 2017. Doctoral Dissertation, University of New South Wales. Accessed March 23, 2019. http://handle.unsw.edu.au/1959.4/58368 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:45859/SOURCE02?view=true.

MLA Handbook (7th Edition):

Han, Fei. “Thermoresponsive Assembly of Plasmonic Nanostructures and their Reversible Tuning of Plasmon Coupling.” 2017. Web. 23 Mar 2019.

Vancouver:

Han F. Thermoresponsive Assembly of Plasmonic Nanostructures and their Reversible Tuning of Plasmon Coupling. [Internet] [Doctoral dissertation]. University of New South Wales; 2017. [cited 2019 Mar 23]. Available from: http://handle.unsw.edu.au/1959.4/58368 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:45859/SOURCE02?view=true.

Council of Science Editors:

Han F. Thermoresponsive Assembly of Plasmonic Nanostructures and their Reversible Tuning of Plasmon Coupling. [Doctoral Dissertation]. University of New South Wales; 2017. Available from: http://handle.unsw.edu.au/1959.4/58368 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:45859/SOURCE02?view=true


Boston College

24. 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 (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 March 23, 2019. 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 Mar 2019.

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 2019 Mar 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

25. 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 March 23, 2019. 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 Mar 2019.

Vancouver:

Edelstein EK. Enantioselective synthesis and stereospecific transformations of organoboronic esters. [Internet] [Doctoral dissertation]. Boston College; 2018. [cited 2019 Mar 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


Boston College

26. Blaisdell, Thomas Powers. New Strategies for Hydroxyl-Directed Organic Reactions.

Degree: PhD, Chemistry, 2015, Boston College

 Described herein are four different research projects spanning over two different research groups. The first two projects describe the development and application of scaffolding catalysts… (more)

Subjects/Keywords: Catalysis; Cross-coupling; Diboration; Hydroformylation; Silylation

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APA (6th Edition):

Blaisdell, T. P. (2015). New Strategies for Hydroxyl-Directed Organic Reactions. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:104626

Chicago Manual of Style (16th Edition):

Blaisdell, Thomas Powers. “New Strategies for Hydroxyl-Directed Organic Reactions.” 2015. Doctoral Dissertation, Boston College. Accessed March 23, 2019. http://dlib.bc.edu/islandora/object/bc-ir:104626.

MLA Handbook (7th Edition):

Blaisdell, Thomas Powers. “New Strategies for Hydroxyl-Directed Organic Reactions.” 2015. Web. 23 Mar 2019.

Vancouver:

Blaisdell TP. New Strategies for Hydroxyl-Directed Organic Reactions. [Internet] [Doctoral dissertation]. Boston College; 2015. [cited 2019 Mar 23]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104626.

Council of Science Editors:

Blaisdell TP. New Strategies for Hydroxyl-Directed Organic Reactions. [Doctoral Dissertation]. Boston College; 2015. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104626


Boston College

27. Chang, Weng Kun. Development of Tandem Reaction for Synthesis of Highly Functionalized Carbocycles.

Degree: MS, Chemistry, 2014, Boston College

 The Suzuki-Miyaura cross-coupling reaction is a common strategy for the formation of a new carbon-carbon bond in organic synthesis. However, intramolecular coupling of allylboron ester… (more)

Subjects/Keywords: allylboron ester; Pt; Suzuki coupling; Synthesis

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APA (6th Edition):

Chang, W. K. (2014). Development of Tandem Reaction for Synthesis of Highly Functionalized Carbocycles. (Masters Thesis). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:104067

Chicago Manual of Style (16th Edition):

Chang, Weng Kun. “Development of Tandem Reaction for Synthesis of Highly Functionalized Carbocycles.” 2014. Masters Thesis, Boston College. Accessed March 23, 2019. http://dlib.bc.edu/islandora/object/bc-ir:104067.

MLA Handbook (7th Edition):

Chang, Weng Kun. “Development of Tandem Reaction for Synthesis of Highly Functionalized Carbocycles.” 2014. Web. 23 Mar 2019.

Vancouver:

Chang WK. Development of Tandem Reaction for Synthesis of Highly Functionalized Carbocycles. [Internet] [Masters thesis]. Boston College; 2014. [cited 2019 Mar 23]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104067.

Council of Science Editors:

Chang WK. Development of Tandem Reaction for Synthesis of Highly Functionalized Carbocycles. [Masters Thesis]. Boston College; 2014. Available from: http://dlib.bc.edu/islandora/object/bc-ir:104067


University of Illinois – Urbana-Champaign

28. Ambrosi, Andrea. I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis.

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

 The first half of the present dissertation describes the mechanistic investigation of the palladium-catalyzed cross-coupling reaction of alkenyl- and arylsilanolates. The combination of reaction kinetics… (more)

Subjects/Keywords: Cross-coupling; Silanolates; Carbon monoxide; Organic synthesis

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APA (6th Edition):

Ambrosi, A. (2016). I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95551

Chicago Manual of Style (16th Edition):

Ambrosi, Andrea. “I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed March 23, 2019. http://hdl.handle.net/2142/95551.

MLA Handbook (7th Edition):

Ambrosi, Andrea. “I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis.” 2016. Web. 23 Mar 2019.

Vancouver:

Ambrosi A. I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/2142/95551.

Council of Science Editors:

Ambrosi A. I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95551


Louisiana State University

29. Ihachi, Moses Inyanje. New strategies for the synthesis of porphyrinoids.

Degree: PhD, Chemistry, 2013, Louisiana State University

 ABSTRACT Chapter 1 describes the most stable isomer of porphyrin called porphycene. In this chapter photodynamic therapy (PDT) is explained, and the application of porphycenes… (more)

Subjects/Keywords: Photodynamic therapy (PDT); Porphyrin isomers (porphyrinoids); Porphycene; Larock indole synthesis; Stille coupling; Suzuki coupling; Ullmann coupling; Tetrapyrroles; Di(2-pyrrolyl)ethenes; Divinylbipyrroles; Olefin metathesis

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APA (6th Edition):

Ihachi, M. I. (2013). New strategies for the synthesis of porphyrinoids. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-11152013-113101 ; https://digitalcommons.lsu.edu/gradschool_dissertations/3186

Chicago Manual of Style (16th Edition):

Ihachi, Moses Inyanje. “New strategies for the synthesis of porphyrinoids.” 2013. Doctoral Dissertation, Louisiana State University. Accessed March 23, 2019. etd-11152013-113101 ; https://digitalcommons.lsu.edu/gradschool_dissertations/3186.

MLA Handbook (7th Edition):

Ihachi, Moses Inyanje. “New strategies for the synthesis of porphyrinoids.” 2013. Web. 23 Mar 2019.

Vancouver:

Ihachi MI. New strategies for the synthesis of porphyrinoids. [Internet] [Doctoral dissertation]. Louisiana State University; 2013. [cited 2019 Mar 23]. Available from: etd-11152013-113101 ; https://digitalcommons.lsu.edu/gradschool_dissertations/3186.

Council of Science Editors:

Ihachi MI. New strategies for the synthesis of porphyrinoids. [Doctoral Dissertation]. Louisiana State University; 2013. Available from: etd-11152013-113101 ; https://digitalcommons.lsu.edu/gradschool_dissertations/3186


University of Texas – Austin

30. O'Keefe, Brian Michael. Synthetic studies on the pluramycin family of antitumor antibiotics : the total synthesis of isokidamycin: Total synthesis of isokidamycin.

Degree: Chemistry, 2010, University of Texas – Austin

 A total synthesis of the complex C-aryl glycoside isokidamycin was achieved during an effort to construct the natural product kidamycin, a member of the pluramycin… (more)

Subjects/Keywords: Total synthesis; Pluramycins; Kidamycin; Isokidamycin; c-aryl glycosides; Natural products; Carbonylative cross-coupling; Cross-coupling; Palladium

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APA (6th Edition):

O'Keefe, B. M. (2010). Synthetic studies on the pluramycin family of antitumor antibiotics : the total synthesis of isokidamycin: Total synthesis of isokidamycin. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2010-12-2035

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):

O'Keefe, Brian Michael. “Synthetic studies on the pluramycin family of antitumor antibiotics : the total synthesis of isokidamycin: Total synthesis of isokidamycin.” 2010. Thesis, University of Texas – Austin. Accessed March 23, 2019. http://hdl.handle.net/2152/ETD-UT-2010-12-2035.

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

MLA Handbook (7th Edition):

O'Keefe, Brian Michael. “Synthetic studies on the pluramycin family of antitumor antibiotics : the total synthesis of isokidamycin: Total synthesis of isokidamycin.” 2010. Web. 23 Mar 2019.

Vancouver:

O'Keefe BM. Synthetic studies on the pluramycin family of antitumor antibiotics : the total synthesis of isokidamycin: Total synthesis of isokidamycin. [Internet] [Thesis]. University of Texas – Austin; 2010. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/2152/ETD-UT-2010-12-2035.

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

Council of Science Editors:

O'Keefe BM. Synthetic studies on the pluramycin family of antitumor antibiotics : the total synthesis of isokidamycin: Total synthesis of isokidamycin. [Thesis]. University of Texas – Austin; 2010. Available from: http://hdl.handle.net/2152/ETD-UT-2010-12-2035

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

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