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Explorations in Novel Photochemical Modes of Radical-Alkene Reactivity : = My Piece of the π.

Record Type:	Electronic resources : Monograph/item
Title/Author:	Explorations in Novel Photochemical Modes of Radical-Alkene Reactivity :/
Reminder of title:	My Piece of the π.
Author:	Campbell, Mark Wesley.
Description:	1 online resource (422 pages)
Notes:	Source: Dissertations Abstracts International, Volume: 84-01, Section: B.
Contained By:	Dissertations Abstracts International84-01B.
Subject:	Organic chemistry. -
Online resource:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=28969442click for full text (PQDT)
ISBN:	9798837517259

Explorations in Novel Photochemical Modes of Radical-Alkene Reactivity : = My Piece of the π.
Campbell, Mark Wesley.

Explorations in Novel Photochemical Modes of Radical-Alkene Reactivity :My Piece of the π. - 1 online resource (422 pages)

Source: Dissertations Abstracts International, Volume: 84-01, Section: B.

Thesis (Ph.D.)--University of Pennsylvania, 2022.

Includes bibliographical references

The formation of Csp3-Csp3 bonds is arguably the most critical transformation in organic synthesis. For many years the Michael addition which utilizes highly reactivity organometallic carbon nucleophiles which are "poised to react" was used to achieve hydroalkylation of activated alkenes. Furthermore, this mode of reactivity also offered the potential to use other electrophiles to perform vicinal (1,2) alkene difunctionalization. Though effective in many contexts this reaction is often plagued by functional group incompatibilities, poor 1,2 vs 1,4 addition selectivity and unstable precursors. In contrast to organometallic carbanions, carbon radicals display much more selective reactivity, particularly with alkenes, and demonstrate much improved chemoselectivity. The Giese addition utilizes carbon radicals typically generated from alkyl halides via halogen atom abstraction to engage in hydroalkylation with activated alkenes. Unfortunately, the harsh conditions and reagents required for the radical chain mechanisms employed in Giese reactions restrict the transformation to alkene hydroalkylations with minimal functional group compatibility. However, several modes of photochemical catalysis can be used for radical generation which are significantly milder and more tolerance than typical radical initiation used in classical Giese addition protocols. These catalytic mechanisms offer the potential for further functionalization of radical addition intermediates opening the door a wide variety of alkene difunctionalizations with dramatically improved functional group compatibility compared to classical vicinal difunctionalizations. Herein are reported personal explorations in novel radical alkene reactions facilitated via photochemical modes of catalysis.

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

Mode of access: World Wide Web

ISBN: 9798837517259Subjects--Topical Terms:

523952
Organic chemistry.
Subjects--Index Terms:

CatalysisIndex Terms--Genre/Form:

542853
Electronic books.

Explorations in Novel Photochemical Modes of Radical-Alkene Reactivity : = My Piece of the π.
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502 $a Thesis (Ph.D.)--University of Pennsylvania, 2022.
504 $a Includes bibliographical references
520 $a The formation of Csp3-Csp3 bonds is arguably the most critical transformation in organic synthesis. For many years the Michael addition which utilizes highly reactivity organometallic carbon nucleophiles which are "poised to react" was used to achieve hydroalkylation of activated alkenes. Furthermore, this mode of reactivity also offered the potential to use other electrophiles to perform vicinal (1,2) alkene difunctionalization. Though effective in many contexts this reaction is often plagued by functional group incompatibilities, poor 1,2 vs 1,4 addition selectivity and unstable precursors. In contrast to organometallic carbanions, carbon radicals display much more selective reactivity, particularly with alkenes, and demonstrate much improved chemoselectivity. The Giese addition utilizes carbon radicals typically generated from alkyl halides via halogen atom abstraction to engage in hydroalkylation with activated alkenes. Unfortunately, the harsh conditions and reagents required for the radical chain mechanisms employed in Giese reactions restrict the transformation to alkene hydroalkylations with minimal functional group compatibility. However, several modes of photochemical catalysis can be used for radical generation which are significantly milder and more tolerance than typical radical initiation used in classical Giese addition protocols. These catalytic mechanisms offer the potential for further functionalization of radical addition intermediates opening the door a wide variety of alkene difunctionalizations with dramatically improved functional group compatibility compared to classical vicinal difunctionalizations. Herein are reported personal explorations in novel radical alkene reactions facilitated via photochemical modes of catalysis.
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