Homogeneous Organic Electron Donors in Transition Metal-Catalyzed Reductive Coupling Reactions /

This thesis summarizes work towards understanding the mechanism of and improving upon nickel-catalyzed reductive coupling reactions through the use of homogeneous organic reductants and understanding of the fundamental reactivity of nickel intermediates. Chapter 1 presents an overview of the utility...

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Bibliographic Details
Main Author: Charboneau, David J. (Author)
Format: Thesis Book
Language:English
Published: [New Haven, Connecticut] : Yale University, 2021
Series:Yale Graduate School of Arts and Sciences Dissertations
Subjects:
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245 1 0 |a Homogeneous Organic Electron Donors in Transition Metal-Catalyzed Reductive Coupling Reactions /  |c David J Charboneau 
264 1 |a [New Haven, Connecticut] :  |b Yale University,  |c 2021 
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380 |a Dissertations, Academic  |2 lcsh 
500 |a Advisors: Hazari, Nilay Committee members: Holland, Patrick; Mayer, James 
500 |a This Yale-originated record is shareable under Creative Commons license CC0  |5 CTY 
502 |b Ph.D  |c Yale University  |d 2021. 
506 |3 EliScholar dissertation:  |a Access is available to the Yale community  |5 CtY 
506 |3 Proquest dissertation:  |a Access is restricted by licensing agreement  |5 CtY 
506 |a This item is not available for online access until February 1, 2023  |5 CtY 
520 |a This thesis summarizes work towards understanding the mechanism of and improving upon nickel-catalyzed reductive coupling reactions through the use of homogeneous organic reductants and understanding of the fundamental reactivity of nickel intermediates. Chapter 1 presents an overview of the utility of homogeneous organic electron donors in nickel-catalyzed reductive coupling reactions. Chapter 2 provides a mechanistic investigation into the nickel-catalyzed carboxylation of aryl halides with carbon dioxide using a homogeneous organic electron donor. In Chapter 3, a general strategy for the cross-electrophile coupling of aryl and alkyl halides is explored. In Chapter 4, the reactivity of a nickel hydride complex supported by a pincer scaffold is explored with small molecules such as N2 and CO 
588 |a Description based on Dissertations Abstracts International, Volume: 83-08, Section: B 
590 |a This item is not available for online access until February 1, 2023. Digital access copies must be provided for use. Contact the Beinecke Rare Book and Manuscript Library at beinecke.library@yale.edu to request access 
650 4 |a Chemistry 
650 4 |a Organic chemistry 
650 4 |a Physical chemistry 
653 |a Organic electron donor 
653 |a Reductive coupling reaction 
653 |a Transition metal 
655 7 |a Academic theses  |2 lcgft 
700 1 |a Hazari, Nilay,  |e degree supervisor 
710 2 |a Yale University  |b Department of Chemistry,  |e degree granting institution. 
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