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Light-Driven Carbene Catalysis for the Synthesis of Carbonyl Compounds.

Record Type:	Electronic resources : Monograph/item
Title/Author:	Light-Driven Carbene Catalysis for the Synthesis of Carbonyl Compounds./
Author:	Bay, Anna V.
Description:	1 online resource (408 pages)
Notes:	Source: Dissertations Abstracts International, Volume: 84-03, Section: B.
Contained By:	Dissertations Abstracts International84-03B.
Subject:	Organic chemistry. -
Online resource:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=29325685click for full text (PQDT)
ISBN:	9798845411082

Light-Driven Carbene Catalysis for the Synthesis of Carbonyl Compounds.
Bay, Anna V.

Light-Driven Carbene Catalysis for the Synthesis of Carbonyl Compounds. - 1 online resource (408 pages)

Source: Dissertations Abstracts International, Volume: 84-03, Section: B.

Thesis (Ph.D.)--Northwestern University, 2022.

Includes bibliographical references

The construction of new C-C bonds remains a central facet of organic chemistry due to its critical role in the synthesis of pharmaceutical compounds and organic materials. Mild and selective methodologies are often required for efficient formation of these bonds in natural product total synthesis, medicinal chemistry campaigns, and more. N-heterocyclic carbenes (NHCs) have emerged as unique Lewis basic catalysts that mediate a range of transformations through umpolung (polarity reversal) reactivity. While the utility of two-electron NHC reactivity has continued to expand, the inability of NHC-derived operators to engage sp3 electrophiles limits their scope, thus highlighting the opportunity for single-electron NHC reactivity. The research described herein focuses on the development of methods at the interface of NHC catalysis and photocatalysis, leveraging the redox properties of each to construct key C-C bonds. Photoredox-catalyzed expansions on these processes are also described.

Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2023

Mode of access: World Wide Web

ISBN: 9798845411082Subjects--Topical Terms:

523952
Organic chemistry.
Subjects--Index Terms:

CarbeneIndex Terms--Genre/Form:

542853
Electronic books.

Light-Driven Carbene Catalysis for the Synthesis of Carbonyl Compounds.
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500 $a Source: Dissertations Abstracts International, Volume: 84-03, Section: B.
500 $a Advisor: Scheidt, Karl.
502 $a Thesis (Ph.D.)--Northwestern University, 2022.
504 $a Includes bibliographical references
520 $a The construction of new C-C bonds remains a central facet of organic chemistry due to its critical role in the synthesis of pharmaceutical compounds and organic materials. Mild and selective methodologies are often required for efficient formation of these bonds in natural product total synthesis, medicinal chemistry campaigns, and more. N-heterocyclic carbenes (NHCs) have emerged as unique Lewis basic catalysts that mediate a range of transformations through umpolung (polarity reversal) reactivity. While the utility of two-electron NHC reactivity has continued to expand, the inability of NHC-derived operators to engage sp3 electrophiles limits their scope, thus highlighting the opportunity for single-electron NHC reactivity. The research described herein focuses on the development of methods at the interface of NHC catalysis and photocatalysis, leveraging the redox properties of each to construct key C-C bonds. Photoredox-catalyzed expansions on these processes are also described.
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538 $a Mode of access: World Wide Web
650 4 $a Organic chemistry. $3 523952
650 4 $a Chemistry. $3 516420
650 4 $a Optics. $3 517925
650 4 $a Chemical engineering. $3 560457
650 4 $a Molecular chemistry. $3 1071612
653 $a Carbene
653 $a Catalysis
653 $a Ketone
653 $a NHC
653 $a Photochemistry
653 $a Photoredox
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773 0 $t Dissertations Abstracts International $g 84-03B.
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