A versatile strategy for difunctionalization of carbon–carbon multiple bonds by photoredox catalysis
Literature Information
Publication Date
2016-05-31
DOI
10.1039/C6QO00139D
Impact Factor
5.281
Authors
Takashi Koike, Munetaka Akita
View Original
Abstract
Photoredox catalysis has emerged as a strong synthetic tool for radical reactions. In particular, a variety of regioselective difunctionalizations of carbon–carbon multiple bonds through SET photoredox processes (oxidative quenching cycle) have been accomplished by an appropriate choice of an electrophilic radical precursor and a nucleophile. The basic concept, representative results and future prospect are the topics of this article.
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Source Journal
Organic Chemistry Frontiers
CiteScore:
7.8
Self-citation Rate:
8.7%
Articles per Year:
724
Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry
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CAS Number:
3089-17-6
Molecular Formula:
C20H10Cl2N2O2
![10-(1-Azabicyclo[2.2.2]oct-3-ylmethyl)-10H-phenothiazine structure](https://static.chemtradehub.com/structs/292/29216-28-2-1d81.webp "10-(1-Azabicyclo[2.2.2]oct-3-ylmethyl)-10H-phenothiazine structure")
10-(1-Azabicyclo[2.2.2]oct-3-ylmethyl)-10H-phenothiazine
CAS Number:
29216-28-2
Molecular Formula:
C20H22N2S
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