자료유형  

 학위논문

Control Number  

0015492454

International Standard Book Number  

9781687932143

Dewey Decimal Classification Number  

547

Main Entry-Personal Name  

Twilton, Jack.

Publication, Distribution, etc. (Imprint  

[Sl] : Princeton University, 2019

Publication, Distribution, etc. (Imprint  

Ann Arbor : ProQuest Dissertations & Theses, 2019

Physical Description  

202 p

General Note  

Source: Dissertations Abstracts International, Volume: 81-05, Section: B.

General Note  

Advisor: MacMillan, David W. C.

Dissertation Note  

Thesis (Ph.D.)--Princeton University, 2019.

Restrictions on Access Note  

This item must not be sold to any third party vendors.

Restrictions on Access Note  

This item must not be added to any third party search indexes.

Summary, Etc.  

요약Transition metal catalyzed cross-coupling is an incredibly powerful platform for the construction of organic architectures, since the advent of these technologies their impact has been felt throughout the chemical sciences and society more broadly. Despite the advances that have been made in this field over the last half century, limitations with respect to the ability to construct Csp3 rich frameworks, and carbon-heteroatom bonds with particularly electron deficient heteroatom coupling partners remains unsolved challenges. The moieties which would result from the realization of these transformations are of long-standing interest in the pharmaceutical industry, and academic medicinal chemistry discovery programs, due to unique biological properties they may possess.Over the last decade photoredox catalysis has arisen as highly versatile platform for forging carbon-carbon and carbon-heteroatom bonds in a variety of molecular settings. In particular the merger of photoredox catalysis and transition metal catalysis has facilitated the development of a litany of new transformations which have the potential to vastly expedite the synthesis of organic frameworks of both academic and industrial interest, many of which have traditionally been difficult or impossible to access with prior art.The design and development of a new paradigm for selective functionalization of C-H bonds adjacent to alcohols (an incredibly prevalent functional handle) is discussed. This strategy utilized a combination of three catalytic cycles in conjunction with a Lewis acid activation mode to access radical species from simple alcohols, which can then be cross coupled with aryl halides to deliver benzylic alcohol products in a highly modular fashion.In addition, a novel cobalt photocatalyzed coupling of N-aryl amides and boronic acids is discussed. The development of a novel cobalt photoexcitation pathway facilitates the coupling of these partners via an open-shell homolytic substitution pathway. This methodology allows access to highly sterically encumbered diaryl amides in excellent yield, and also highlights the potential utility of base-metal chromophores in photocatalysis.

Subject Added Entry-Topical Term  

Chemistry

Subject Added Entry-Topical Term  

Organic chemistry

Added Entry-Corporate Name  

Princeton University Chemistry

Host Item Entry  

Dissertations Abstracts International. 81-05B.

Host Item Entry  

Dissertation Abstract International

Electronic Location and Access  

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Control Number  

joongbu:565267