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You searched for subject:(Cross Coupling). Showing records 1 – 30 of 345 total matches.

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University of Illinois – Urbana-Champaign

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

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 September 19, 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. 19 Sep 2019.

Vancouver:

Yousaf Z. Development of organosilicon cross-coupling reaction. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Sep 19]. 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


University of Ottawa

2. Masson-Makdissi, Jeanne. Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles .

Degree: 2018, University of Ottawa

 First popularized in the 1970s, transition metal-catalyzed cross-couplings now constitute staple reactions for the formation of carbon-carbon and carbon-heteroatom bonds. Recent endeavours in the field… (more)

Subjects/Keywords: cross-coupling; esters

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APA (6th Edition):

Masson-Makdissi, J. (2018). Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/38398

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):

Masson-Makdissi, Jeanne. “Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles .” 2018. Thesis, University of Ottawa. Accessed September 19, 2019. http://hdl.handle.net/10393/38398.

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

MLA Handbook (7th Edition):

Masson-Makdissi, Jeanne. “Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles .” 2018. Web. 19 Sep 2019.

Vancouver:

Masson-Makdissi J. Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles . [Internet] [Thesis]. University of Ottawa; 2018. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/10393/38398.

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

Council of Science Editors:

Masson-Makdissi J. Controlling Selectivity in Cross-Coupling Reactions with Ester Electrophiles . [Thesis]. University of Ottawa; 2018. Available from: http://hdl.handle.net/10393/38398

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


Queens University

3. Holland, Amy Marie. INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS .

Degree: Chemistry, 2010, Queens University

 Until recently, secondary organoboronic esters were not viable substrates in the Suzuki-Miyaura cross-coupling reaction; however under recently reported conditions from the Crudden group1, which includes… (more)

Subjects/Keywords: Organometallics; Cross-Coupling

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APA (6th Edition):

Holland, A. M. (2010). INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/6071

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):

Holland, Amy Marie. “INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS .” 2010. Thesis, Queens University. Accessed September 19, 2019. http://hdl.handle.net/1974/6071.

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

MLA Handbook (7th Edition):

Holland, Amy Marie. “INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS .” 2010. Web. 19 Sep 2019.

Vancouver:

Holland AM. INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS . [Internet] [Thesis]. Queens University; 2010. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/1974/6071.

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

Council of Science Editors:

Holland AM. INVESTIGATIONS INTO CROSS-COUPLING OF SECONDARY ORGANOBORONIC ESTERS . [Thesis]. Queens University; 2010. Available from: http://hdl.handle.net/1974/6071

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


University of California – Irvine

4. 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 September 19, 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. 19 Sep 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 Sep 19]. 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


Dalhousie University

5. Lundgren, Rylan. Design and Application of P,N-Ligands for Platinum-Group Metal Catalyzed Reactions.

Degree: PhD, Department of Chemistry, 2010, Dalhousie University

 Homogeneous organometallic species serve as useful catalysts for a vast number of chemical transformations. Ancillary ligands which bind to the metal center are employed to… (more)

Subjects/Keywords: Catalysis; organometallic; cross-coupling; hydrogenation

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APA (6th Edition):

Lundgren, R. (2010). Design and Application of P,N-Ligands for Platinum-Group Metal Catalyzed Reactions. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/13115

Chicago Manual of Style (16th Edition):

Lundgren, Rylan. “Design and Application of P,N-Ligands for Platinum-Group Metal Catalyzed Reactions.” 2010. Doctoral Dissertation, Dalhousie University. Accessed September 19, 2019. http://hdl.handle.net/10222/13115.

MLA Handbook (7th Edition):

Lundgren, Rylan. “Design and Application of P,N-Ligands for Platinum-Group Metal Catalyzed Reactions.” 2010. Web. 19 Sep 2019.

Vancouver:

Lundgren R. Design and Application of P,N-Ligands for Platinum-Group Metal Catalyzed Reactions. [Internet] [Doctoral dissertation]. Dalhousie University; 2010. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/10222/13115.

Council of Science Editors:

Lundgren R. Design and Application of P,N-Ligands for Platinum-Group Metal Catalyzed Reactions. [Doctoral Dissertation]. Dalhousie University; 2010. Available from: http://hdl.handle.net/10222/13115


Princeton University

6. Arendt, Kevin Michael. Engaging α-Oxy Radicals in Nickel-Catalyzed Cross Coupling Reactions .

Degree: PhD, 2016, Princeton University

 Transition metal-catalyzed cross coupling reactions have transformed the way in which chemists construct the C–C framework of organic molecules. This strategy has seen broad use… (more)

Subjects/Keywords: catalysis; Cross-coupling; nickel; radicals

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APA (6th Edition):

Arendt, K. M. (2016). Engaging α-Oxy Radicals in Nickel-Catalyzed Cross Coupling Reactions . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01sx61dp71q

Chicago Manual of Style (16th Edition):

Arendt, Kevin Michael. “Engaging α-Oxy Radicals in Nickel-Catalyzed Cross Coupling Reactions .” 2016. Doctoral Dissertation, Princeton University. Accessed September 19, 2019. http://arks.princeton.edu/ark:/88435/dsp01sx61dp71q.

MLA Handbook (7th Edition):

Arendt, Kevin Michael. “Engaging α-Oxy Radicals in Nickel-Catalyzed Cross Coupling Reactions .” 2016. Web. 19 Sep 2019.

Vancouver:

Arendt KM. Engaging α-Oxy Radicals in Nickel-Catalyzed Cross Coupling Reactions . [Internet] [Doctoral dissertation]. Princeton University; 2016. [cited 2019 Sep 19]. Available from: http://arks.princeton.edu/ark:/88435/dsp01sx61dp71q.

Council of Science Editors:

Arendt KM. Engaging α-Oxy Radicals in Nickel-Catalyzed Cross Coupling Reactions . [Doctoral Dissertation]. Princeton University; 2016. Available from: http://arks.princeton.edu/ark:/88435/dsp01sx61dp71q


University of Rochester

7. Prinsell, Michael R. (1986 - ). Nickel-catalyzed reductive coupling of alkyl, allyl and vinyl electrophiles.

Degree: PhD, 2014, University of Rochester

 The nickel-catalyzed reductive coupling of two organic electrophiles to form new carbon-carbon bonds is a fast emerging field of chemistry, with applications to the synthesis… (more)

Subjects/Keywords: Nickel; Electrophile; Cross-coupling

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APA (6th Edition):

Prinsell, M. R. (. -. ). (2014). Nickel-catalyzed reductive coupling of alkyl, allyl and vinyl electrophiles. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/28613

Chicago Manual of Style (16th Edition):

Prinsell, Michael R (1986 - ). “Nickel-catalyzed reductive coupling of alkyl, allyl and vinyl electrophiles.” 2014. Doctoral Dissertation, University of Rochester. Accessed September 19, 2019. http://hdl.handle.net/1802/28613.

MLA Handbook (7th Edition):

Prinsell, Michael R (1986 - ). “Nickel-catalyzed reductive coupling of alkyl, allyl and vinyl electrophiles.” 2014. Web. 19 Sep 2019.

Vancouver:

Prinsell MR(-). Nickel-catalyzed reductive coupling of alkyl, allyl and vinyl electrophiles. [Internet] [Doctoral dissertation]. University of Rochester; 2014. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/1802/28613.

Council of Science Editors:

Prinsell MR(-). Nickel-catalyzed reductive coupling of alkyl, allyl and vinyl electrophiles. [Doctoral Dissertation]. University of Rochester; 2014. Available from: http://hdl.handle.net/1802/28613


Boston College

8. 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 September 19, 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. 19 Sep 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 Sep 19]. 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

9. 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 September 19, 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. 19 Sep 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 Sep 19]. 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

10. 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 September 19, 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. 19 Sep 2019.

Vancouver:

Schuster CH. Synthesis and Utility of Organoboron Reagents for Enantioselective Synthesis. [Internet] [Doctoral dissertation]. Boston College; 2014. [cited 2019 Sep 19]. 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

11. Hammoud, Sokaina. Accès à de nouvelles structures tricycliques di-iodes à base indolique et isoindolique par iodocyclisation : Access to new di-iodinated tricyclic structures based on indoles and isoindoles by iodocyclization.

Degree: Docteur es, Chimie organique, 2015, Université François-Rabelais de Tours

Une nouvelle voie d’accès à des structures tri-cycliques originaux les « oxazino-indole di-iodés» a été mise au point à partir des acides 1H-indole-2-carboxyliques commerciaux ou… (more)

Subjects/Keywords: Indoles; Isoindoles; Iodocyclisation; Cross-coupling; Indoles; Isoindoles; Iodocyclization; Cross-coupling

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APA (6th Edition):

Hammoud, S. (2015). Accès à de nouvelles structures tricycliques di-iodes à base indolique et isoindolique par iodocyclisation : Access to new di-iodinated tricyclic structures based on indoles and isoindoles by iodocyclization. (Doctoral Dissertation). Université François-Rabelais de Tours. Retrieved from http://www.theses.fr/2015TOUR4034

Chicago Manual of Style (16th Edition):

Hammoud, Sokaina. “Accès à de nouvelles structures tricycliques di-iodes à base indolique et isoindolique par iodocyclisation : Access to new di-iodinated tricyclic structures based on indoles and isoindoles by iodocyclization.” 2015. Doctoral Dissertation, Université François-Rabelais de Tours. Accessed September 19, 2019. http://www.theses.fr/2015TOUR4034.

MLA Handbook (7th Edition):

Hammoud, Sokaina. “Accès à de nouvelles structures tricycliques di-iodes à base indolique et isoindolique par iodocyclisation : Access to new di-iodinated tricyclic structures based on indoles and isoindoles by iodocyclization.” 2015. Web. 19 Sep 2019.

Vancouver:

Hammoud S. Accès à de nouvelles structures tricycliques di-iodes à base indolique et isoindolique par iodocyclisation : Access to new di-iodinated tricyclic structures based on indoles and isoindoles by iodocyclization. [Internet] [Doctoral dissertation]. Université François-Rabelais de Tours; 2015. [cited 2019 Sep 19]. Available from: http://www.theses.fr/2015TOUR4034.

Council of Science Editors:

Hammoud S. Accès à de nouvelles structures tricycliques di-iodes à base indolique et isoindolique par iodocyclisation : Access to new di-iodinated tricyclic structures based on indoles and isoindoles by iodocyclization. [Doctoral Dissertation]. Université François-Rabelais de Tours; 2015. Available from: http://www.theses.fr/2015TOUR4034


University of California – San Diego

12. 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 September 19, 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. 19 Sep 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 Sep 19]. 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

13. 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 September 19, 2019. http://hdl.handle.net/2142/91591.

MLA Handbook (7th Edition):

Gillis, Eric P. “Iterative cross-coupling with MIDA boronates.” 2010. Web. 19 Sep 2019.

Vancouver:

Gillis EP. Iterative cross-coupling with MIDA boronates. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Sep 19]. 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


University of California – Irvine

14. 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 September 19, 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. 19 Sep 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 Sep 19]. 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

15. 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 September 19, 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. 19 Sep 2019.

Vancouver:

Tollefson EJ. Development of Stereospecific Nickel-Catalyzed Cross-Coupling Reactions. [Internet] [Thesis]. University of California – Irvine; 2016. [cited 2019 Sep 19]. 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

16. 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 September 19, 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. 19 Sep 2019.

Vancouver:

Harris M. Development of Stereospecific Nickel-Catalyzed Transformations of Benzylic Alcohol Derivatives. [Internet] [Thesis]. University of California – Irvine; 2015. [cited 2019 Sep 19]. 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 Illinois – Urbana-Champaign

17. 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 September 19, 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. 19 Sep 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 Sep 19]. 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


King Abdullah University of Science and Technology

18. 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 September 19, 2019. 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. 19 Sep 2019.

Vancouver:

Walter PE. Optimization of an Efficient and Sustainable Sonogashira Cross-Coupling Protocol. [Internet] [Thesis]. King Abdullah University of Science and Technology; 2012. [cited 2019 Sep 19]. 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

19. Hua, Xi Ye. Expanding the Scope of Coupling Partners in Catalytic Cross-Coupling Reactions .

Degree: 2016, University of Ottawa

 Carbon-carbon (C-C) bond formation is among the most important processes in organic chemistry. Transition metal catalyzed C-C bond formation is an active research area that… (more)

Subjects/Keywords: cross coupling

…on cross-coupling reactions through July 2016… …expand the scope of the Kumada-Corriu cross-coupling reaction. The strategy to achieve this… …other sensitive functionalities are all demonstrated to undergo chemoselective cross-coupling… …Chemoselectivity in the Kumada–Corriu Cross-Coupling Reaction, ” Hua, X.Y.; Masson-Makdissi, J.; Sullivan… …development of olefin metathesis. Cross-coupling is a generic term for a variety of reactions where… 

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APA (6th Edition):

Hua, X. Y. (2016). Expanding the Scope of Coupling Partners in Catalytic Cross-Coupling Reactions . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/35521

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):

Hua, Xi Ye. “Expanding the Scope of Coupling Partners in Catalytic Cross-Coupling Reactions .” 2016. Thesis, University of Ottawa. Accessed September 19, 2019. http://hdl.handle.net/10393/35521.

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

MLA Handbook (7th Edition):

Hua, Xi Ye. “Expanding the Scope of Coupling Partners in Catalytic Cross-Coupling Reactions .” 2016. Web. 19 Sep 2019.

Vancouver:

Hua XY. Expanding the Scope of Coupling Partners in Catalytic Cross-Coupling Reactions . [Internet] [Thesis]. University of Ottawa; 2016. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/10393/35521.

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

Council of Science Editors:

Hua XY. Expanding the Scope of Coupling Partners in Catalytic Cross-Coupling Reactions . [Thesis]. University of Ottawa; 2016. Available from: http://hdl.handle.net/10393/35521

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

20. Wang, Liqiong. Synthesis Of 2-Boron Substituted-1,3-Dienes And Their Diels-Alder/Suzuki Cross Coupling Reactions.

Degree: 2012, Wake Forest University

Dissertation under the direction of Mark E. Welker, Ph.D., Professor of Department of Chemistry, Wake Forest University

Subjects/Keywords: Cross Coupling

…79 CHAPTER 4 4.1 Suzuki Cross Coupling Reactions… …87 4.1.1 Suzuki Cross Coupling Reactions… …87 4.1.2 Tandem Diels-Alder/Suzuki Cross Coupling Reactions… …5 Figure 1.5 General Catalytic Cycle for Suzuki-Miyaura, Heck And Stille Cross-Coupling… …78 Table V Optimization of Suzuki Cross Coupling Reaction… 

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APA (6th Edition):

Wang, L. (2012). Synthesis Of 2-Boron Substituted-1,3-Dienes And Their Diels-Alder/Suzuki Cross Coupling Reactions. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/37436

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):

Wang, Liqiong. “Synthesis Of 2-Boron Substituted-1,3-Dienes And Their Diels-Alder/Suzuki Cross Coupling Reactions.” 2012. Thesis, Wake Forest University. Accessed September 19, 2019. http://hdl.handle.net/10339/37436.

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

MLA Handbook (7th Edition):

Wang, Liqiong. “Synthesis Of 2-Boron Substituted-1,3-Dienes And Their Diels-Alder/Suzuki Cross Coupling Reactions.” 2012. Web. 19 Sep 2019.

Vancouver:

Wang L. Synthesis Of 2-Boron Substituted-1,3-Dienes And Their Diels-Alder/Suzuki Cross Coupling Reactions. [Internet] [Thesis]. Wake Forest University; 2012. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/10339/37436.

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

Council of Science Editors:

Wang L. Synthesis Of 2-Boron Substituted-1,3-Dienes And Their Diels-Alder/Suzuki Cross Coupling Reactions. [Thesis]. Wake Forest University; 2012. Available from: http://hdl.handle.net/10339/37436

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

21. Junker, Christopher Sean. 2-Silicon-Substituted 1,3-Dienes: Participants in Diels-Alder Chemistry and Metal-Mediated Processes.

Degree: 2011, Wake Forest University

 Two of the major focuses in current synthetic organic chemistry are asymmetric carbon-carbon bond forming processes and catalytic one-pot reactions. Two processes that are of… (more)

Subjects/Keywords: Cross-Coupling

Cross-Coupling 26 Figure 1.15 Cross-Coupling of Safety-Catch Silanols 29 Figure 1.16 Auto… …Tandem Catalysis 31 IX Figure 2.1 Diels–Alder/Cross-Coupling Reaction of 2-Silyl-1,3… …Cross-Coupling Catalytic Cycle 128 Figure 5.2 Computational Model of Oxidative Addition to… …Cross-Coupling Conditions 67 Table IX. Scope of Cross-Coupling Reaction 68 Table X… …research are the Diels–Alder reaction and transition-metalcatalyzed cross-coupling reactions… 

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APA (6th Edition):

Junker, C. S. (2011). 2-Silicon-Substituted 1,3-Dienes: Participants in Diels-Alder Chemistry and Metal-Mediated Processes. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/36145

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):

Junker, Christopher Sean. “2-Silicon-Substituted 1,3-Dienes: Participants in Diels-Alder Chemistry and Metal-Mediated Processes.” 2011. Thesis, Wake Forest University. Accessed September 19, 2019. http://hdl.handle.net/10339/36145.

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

MLA Handbook (7th Edition):

Junker, Christopher Sean. “2-Silicon-Substituted 1,3-Dienes: Participants in Diels-Alder Chemistry and Metal-Mediated Processes.” 2011. Web. 19 Sep 2019.

Vancouver:

Junker CS. 2-Silicon-Substituted 1,3-Dienes: Participants in Diels-Alder Chemistry and Metal-Mediated Processes. [Internet] [Thesis]. Wake Forest University; 2011. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/10339/36145.

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

Council of Science Editors:

Junker CS. 2-Silicon-Substituted 1,3-Dienes: Participants in Diels-Alder Chemistry and Metal-Mediated Processes. [Thesis]. Wake Forest University; 2011. Available from: http://hdl.handle.net/10339/36145

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

22. Pidaparthi, Ramakrishna Reddy. TRANSITION METAL MEDIATED, STEREOSELECTIVE HIGHER-ORDER [6+4] AND DIELS-ALDER [4+2] CYCLOADDITION REACTIONS: SYNTHESIS OF NOVEL 2-SILYL SUBSTITUTED-1,3-DIENYL COMPOUNDS AND THEIR DOMINO REACTIONS.

Degree: 2011, Wake Forest University

 We have prepared various substituted cobaloxime dienes and studied extensively their reactivities in Diels-Alder reactions. Based on the studies with cobaloxime chemistry, we concluded that… (more)

Subjects/Keywords: cross coupling

…Cycloadditions 50 54 10) Literature Review on Cross-Coupling Reactions 10.1) Fluoride… …Assisted Cross-Coupling Reactions of Silanes 10.1.1) Cross-Coupling Reactions of Vinyl… …Silanes 10.1.2) Cross-Coupling Reactions of Aryl Silanes 10.2) Non-Fluoride Mediated… …Cross-Coupling Reactions of Silanes 62 63 69 72 11) A Brief outlook on: 11.1)… …siloxacycles, 9.2.29 62 Scheme – 10.1 Schematic representation of cross-coupling reactions 62… 

Page 1 Page 2 Page 3 Page 4 Page 5

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APA (6th Edition):

Pidaparthi, R. R. (2011). TRANSITION METAL MEDIATED, STEREOSELECTIVE HIGHER-ORDER [6+4] AND DIELS-ALDER [4+2] CYCLOADDITION REACTIONS: SYNTHESIS OF NOVEL 2-SILYL SUBSTITUTED-1,3-DIENYL COMPOUNDS AND THEIR DOMINO REACTIONS. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/36160

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):

Pidaparthi, Ramakrishna Reddy. “TRANSITION METAL MEDIATED, STEREOSELECTIVE HIGHER-ORDER [6+4] AND DIELS-ALDER [4+2] CYCLOADDITION REACTIONS: SYNTHESIS OF NOVEL 2-SILYL SUBSTITUTED-1,3-DIENYL COMPOUNDS AND THEIR DOMINO REACTIONS.” 2011. Thesis, Wake Forest University. Accessed September 19, 2019. http://hdl.handle.net/10339/36160.

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

MLA Handbook (7th Edition):

Pidaparthi, Ramakrishna Reddy. “TRANSITION METAL MEDIATED, STEREOSELECTIVE HIGHER-ORDER [6+4] AND DIELS-ALDER [4+2] CYCLOADDITION REACTIONS: SYNTHESIS OF NOVEL 2-SILYL SUBSTITUTED-1,3-DIENYL COMPOUNDS AND THEIR DOMINO REACTIONS.” 2011. Web. 19 Sep 2019.

Vancouver:

Pidaparthi RR. TRANSITION METAL MEDIATED, STEREOSELECTIVE HIGHER-ORDER [6+4] AND DIELS-ALDER [4+2] CYCLOADDITION REACTIONS: SYNTHESIS OF NOVEL 2-SILYL SUBSTITUTED-1,3-DIENYL COMPOUNDS AND THEIR DOMINO REACTIONS. [Internet] [Thesis]. Wake Forest University; 2011. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/10339/36160.

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

Council of Science Editors:

Pidaparthi RR. TRANSITION METAL MEDIATED, STEREOSELECTIVE HIGHER-ORDER [6+4] AND DIELS-ALDER [4+2] CYCLOADDITION REACTIONS: SYNTHESIS OF NOVEL 2-SILYL SUBSTITUTED-1,3-DIENYL COMPOUNDS AND THEIR DOMINO REACTIONS. [Thesis]. Wake Forest University; 2011. Available from: http://hdl.handle.net/10339/36160

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


University of South Africa

23. Oyeyiola, Felix Adetunji. Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones .

Degree: 2011, University of South Africa

 The 2-aryl-2,3-dihydroquinolin-4(1H)-ones were prepared via acid-catalyzed cyclization of the corresponding 2-aminochalcones, which were in turn, prepared by base-promoted Claisen-Schmidt aldol condensation of 2-aminoacetophenone and benzaldehyde… (more)

Subjects/Keywords: 2-aminochalcones; Cross-coupling reaction; Suzuki-Miyaura

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APA (6th Edition):

Oyeyiola, F. A. (2011). Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones . (Masters Thesis). University of South Africa. Retrieved from http://hdl.handle.net/10500/5842

Chicago Manual of Style (16th Edition):

Oyeyiola, Felix Adetunji. “Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones .” 2011. Masters Thesis, University of South Africa. Accessed September 19, 2019. http://hdl.handle.net/10500/5842.

MLA Handbook (7th Edition):

Oyeyiola, Felix Adetunji. “Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones .” 2011. Web. 19 Sep 2019.

Vancouver:

Oyeyiola FA. Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones . [Internet] [Masters thesis]. University of South Africa; 2011. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/10500/5842.

Council of Science Editors:

Oyeyiola FA. Synthesis and transformation of the 2,6,8-triaryl-2,3-dihydroquinolin-4(1H)-ones . [Masters Thesis]. University of South Africa; 2011. Available from: http://hdl.handle.net/10500/5842


Virginia Commonwealth University

24. ELAZAB, HANY. Graphene-Supported Metal Nanoparticles For Applications in Heterogeneous Catalysis.

Degree: PhD, Engineering, 2013, Virginia Commonwealth University

  Due to its unique properties and high surface area, Graphene has become a good candidate as an effective solid support for metal catalysts. The… (more)

Subjects/Keywords: heterogeneous catalysis; nanoparticles; cross coupling; graphene.; Engineering

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APA (6th Edition):

ELAZAB, H. (2013). Graphene-Supported Metal Nanoparticles For Applications in Heterogeneous Catalysis. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/560

Chicago Manual of Style (16th Edition):

ELAZAB, HANY. “Graphene-Supported Metal Nanoparticles For Applications in Heterogeneous Catalysis.” 2013. Doctoral Dissertation, Virginia Commonwealth University. Accessed September 19, 2019. https://scholarscompass.vcu.edu/etd/560.

MLA Handbook (7th Edition):

ELAZAB, HANY. “Graphene-Supported Metal Nanoparticles For Applications in Heterogeneous Catalysis.” 2013. Web. 19 Sep 2019.

Vancouver:

ELAZAB H. Graphene-Supported Metal Nanoparticles For Applications in Heterogeneous Catalysis. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2013. [cited 2019 Sep 19]. Available from: https://scholarscompass.vcu.edu/etd/560.

Council of Science Editors:

ELAZAB H. Graphene-Supported Metal Nanoparticles For Applications in Heterogeneous Catalysis. [Doctoral Dissertation]. Virginia Commonwealth University; 2013. Available from: https://scholarscompass.vcu.edu/etd/560


University of Toronto

25. Borduas, Nadine. Oxidative Palladium(II)-catalyzed Arene C-H Bond Functionalization and Progress towards the Total Synthesis of 6-Deoxyerythronolide B.

Degree: 2012, University of Toronto

To address the issue of unnecessary functional group transformations in synthesis, the direct functionalization of carbon-hydrogen (C―H) bonds presents itself as an efficient and atom… (more)

Subjects/Keywords: oxidative cross coupling; total synthesis; 0490

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APA (6th Edition):

Borduas, N. (2012). Oxidative Palladium(II)-catalyzed Arene C-H Bond Functionalization and Progress towards the Total Synthesis of 6-Deoxyerythronolide B. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/32228

Chicago Manual of Style (16th Edition):

Borduas, Nadine. “Oxidative Palladium(II)-catalyzed Arene C-H Bond Functionalization and Progress towards the Total Synthesis of 6-Deoxyerythronolide B.” 2012. Masters Thesis, University of Toronto. Accessed September 19, 2019. http://hdl.handle.net/1807/32228.

MLA Handbook (7th Edition):

Borduas, Nadine. “Oxidative Palladium(II)-catalyzed Arene C-H Bond Functionalization and Progress towards the Total Synthesis of 6-Deoxyerythronolide B.” 2012. Web. 19 Sep 2019.

Vancouver:

Borduas N. Oxidative Palladium(II)-catalyzed Arene C-H Bond Functionalization and Progress towards the Total Synthesis of 6-Deoxyerythronolide B. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/1807/32228.

Council of Science Editors:

Borduas N. Oxidative Palladium(II)-catalyzed Arene C-H Bond Functionalization and Progress towards the Total Synthesis of 6-Deoxyerythronolide B. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/32228


University of New Mexico

26. Shrestha, Bijay. Catalytic Functionalization of Organoaluminum Reagents and Olefins by Cross-Coupling with Copper and Nickel.

Degree: Department of Chemistry and Chemical Biology, 2018, University of New Mexico

  This thesis is divided into two parts. The first part focuses on the Cu-catalyzed cross-coupling of organoaluminum reagents with organohalides. One of the most… (more)

Subjects/Keywords: Cross-coupling; Dicarbofunctionalization; Chemistry; Organic Chemistry

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APA (6th Edition):

Shrestha, B. (2018). Catalytic Functionalization of Organoaluminum Reagents and Olefins by Cross-Coupling with Copper and Nickel. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/chem_etds/99

Chicago Manual of Style (16th Edition):

Shrestha, Bijay. “Catalytic Functionalization of Organoaluminum Reagents and Olefins by Cross-Coupling with Copper and Nickel.” 2018. Doctoral Dissertation, University of New Mexico. Accessed September 19, 2019. https://digitalrepository.unm.edu/chem_etds/99.

MLA Handbook (7th Edition):

Shrestha, Bijay. “Catalytic Functionalization of Organoaluminum Reagents and Olefins by Cross-Coupling with Copper and Nickel.” 2018. Web. 19 Sep 2019.

Vancouver:

Shrestha B. Catalytic Functionalization of Organoaluminum Reagents and Olefins by Cross-Coupling with Copper and Nickel. [Internet] [Doctoral dissertation]. University of New Mexico; 2018. [cited 2019 Sep 19]. Available from: https://digitalrepository.unm.edu/chem_etds/99.

Council of Science Editors:

Shrestha B. Catalytic Functionalization of Organoaluminum Reagents and Olefins by Cross-Coupling with Copper and Nickel. [Doctoral Dissertation]. University of New Mexico; 2018. Available from: https://digitalrepository.unm.edu/chem_etds/99


University of Illinois – Urbana-Champaign

27. Davis, Erin. An iterative cross-coupling based approach to the synthesis of peridinin and progress towards peridinin derivatives.

Degree: MS, 0335, 2013, University of Illinois – Urbana-Champaign

 Lipoperoxidation plays a role in diseases such as atherosclerosis, rheumatoid arthritis, cancer, and may contribute to the general phenomenon of aging. As individuals with deficiencies… (more)

Subjects/Keywords: peridinin; lipoperoxidation; carotenoids; iterative cross coupling

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APA (6th Edition):

Davis, E. (2013). An iterative cross-coupling based approach to the synthesis of peridinin and progress towards peridinin derivatives. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/45557

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):

Davis, Erin. “An iterative cross-coupling based approach to the synthesis of peridinin and progress towards peridinin derivatives.” 2013. Thesis, University of Illinois – Urbana-Champaign. Accessed September 19, 2019. http://hdl.handle.net/2142/45557.

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

MLA Handbook (7th Edition):

Davis, Erin. “An iterative cross-coupling based approach to the synthesis of peridinin and progress towards peridinin derivatives.” 2013. Web. 19 Sep 2019.

Vancouver:

Davis E. An iterative cross-coupling based approach to the synthesis of peridinin and progress towards peridinin derivatives. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/2142/45557.

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

Council of Science Editors:

Davis E. An iterative cross-coupling based approach to the synthesis of peridinin and progress towards peridinin derivatives. [Thesis]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/45557

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


University of Illinois – Urbana-Champaign

28. Huang, David S. Part I. Large scale procedure for the ??-arylation of esters catalyzed by the pd(i) dimer [p(tbu)3]pd(??-br)]2. Part II. Palladium-catalyzed ??-arylation of ??,??-unsaturated esters.

Degree: MS, 0335, 2010, University of Illinois – Urbana-Champaign

 We report the development of a procedure for the ??-arylation of esters on 42 mmol scale which did not require use of a glovebox. The… (more)

Subjects/Keywords: cross-coupling; enolates; homogeneous catalysis; palladium

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APA (6th Edition):

Huang, D. S. (2010). Part I. Large scale procedure for the ??-arylation of esters catalyzed by the pd(i) dimer [p(tbu)3]pd(??-br)]2. Part II. Palladium-catalyzed ??-arylation of ??,??-unsaturated esters. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/16816

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

Chicago Manual of Style (16th Edition):

Huang, David S. “Part I. Large scale procedure for the ??-arylation of esters catalyzed by the pd(i) dimer [p(tbu)3]pd(??-br)]2. Part II. Palladium-catalyzed ??-arylation of ??,??-unsaturated esters.” 2010. Thesis, University of Illinois – Urbana-Champaign. Accessed September 19, 2019. http://hdl.handle.net/2142/16816.

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

MLA Handbook (7th Edition):

Huang, David S. “Part I. Large scale procedure for the ??-arylation of esters catalyzed by the pd(i) dimer [p(tbu)3]pd(??-br)]2. Part II. Palladium-catalyzed ??-arylation of ??,??-unsaturated esters.” 2010. Web. 19 Sep 2019.

Vancouver:

Huang DS. Part I. Large scale procedure for the ??-arylation of esters catalyzed by the pd(i) dimer [p(tbu)3]pd(??-br)]2. Part II. Palladium-catalyzed ??-arylation of ??,??-unsaturated esters. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/2142/16816.

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

Council of Science Editors:

Huang DS. Part I. Large scale procedure for the ??-arylation of esters catalyzed by the pd(i) dimer [p(tbu)3]pd(??-br)]2. Part II. Palladium-catalyzed ??-arylation of ??,??-unsaturated esters. [Thesis]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/16816

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


Victoria University of Wellington

29. Moore, Peter William. Synthesis of 2-C-Branched Sugars.

Degree: 2012, Victoria University of Wellington

 A range of unnatural carbohydrates (sugars) with an unusual 2-C-bromomethylene branch have been synthesised by reaction of the 1,2-cyclopropanated carbohydrate 52 with different nucleophiles. Initial… (more)

Subjects/Keywords: Cyclopropane; C-branch sugars; Cross-coupling

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

APA (6th Edition):

Moore, P. W. (2012). Synthesis of 2-C-Branched Sugars. (Masters Thesis). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/2404

Chicago Manual of Style (16th Edition):

Moore, Peter William. “Synthesis of 2-C-Branched Sugars.” 2012. Masters Thesis, Victoria University of Wellington. Accessed September 19, 2019. http://hdl.handle.net/10063/2404.

MLA Handbook (7th Edition):

Moore, Peter William. “Synthesis of 2-C-Branched Sugars.” 2012. Web. 19 Sep 2019.

Vancouver:

Moore PW. Synthesis of 2-C-Branched Sugars. [Internet] [Masters thesis]. Victoria University of Wellington; 2012. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/10063/2404.

Council of Science Editors:

Moore PW. Synthesis of 2-C-Branched Sugars. [Masters Thesis]. Victoria University of Wellington; 2012. Available from: http://hdl.handle.net/10063/2404


University of Rochester

30. Everson, Daniel A. (1985 - ). Nickel-catalyzed electrophile cross-coupling of aryl halides with alkyl halides.

Degree: PhD, 2014, University of Rochester

 This thesis details the author’s contributions to the emerging field of electrophile cross-couplings. This new field is related to the well-established field of conventional cross-coupling(more)

Subjects/Keywords: Catalysis; Cross coupling; Manganese; Nickel; Reductive; Zinc

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APA (6th Edition):

Everson, D. A. (. -. ). (2014). Nickel-catalyzed electrophile cross-coupling of aryl halides with alkyl halides. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/28128

Chicago Manual of Style (16th Edition):

Everson, Daniel A (1985 - ). “Nickel-catalyzed electrophile cross-coupling of aryl halides with alkyl halides.” 2014. Doctoral Dissertation, University of Rochester. Accessed September 19, 2019. http://hdl.handle.net/1802/28128.

MLA Handbook (7th Edition):

Everson, Daniel A (1985 - ). “Nickel-catalyzed electrophile cross-coupling of aryl halides with alkyl halides.” 2014. Web. 19 Sep 2019.

Vancouver:

Everson DA(-). Nickel-catalyzed electrophile cross-coupling of aryl halides with alkyl halides. [Internet] [Doctoral dissertation]. University of Rochester; 2014. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/1802/28128.

Council of Science Editors:

Everson DA(-). Nickel-catalyzed electrophile cross-coupling of aryl halides with alkyl halides. [Doctoral Dissertation]. University of Rochester; 2014. Available from: http://hdl.handle.net/1802/28128

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