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Synlett 2012; 23(18): 2707-2713
DOI: 10.1055/s-0032-1317349
DOI: 10.1055/s-0032-1317349
letter
Reusable Visible Light Photoredox Catalysts; Catalyzed Benzylic C(sp3)–H Functionalization/Carbocyclization Reactions
Further Information
Publication History
Received: 09 August 2012
Accepted after revision: 11 September 2012
Publication Date:
18 October 2012 (online)
Abstract
The C(sp3)–H functionalization/carbocyclization reaction through the oxidative quenching of visible light photoredox catalysts is established for constructing functionalized 1H-indenes. The process is general for a wide range of benzylic C(sp3)–H bonds and is highly compatible with common functional groups. Importantly, the visible light photoredox catalysts can be recovered and reused at least three times without loss of catalytic activity.
Supporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synlett.
- Supporting Information
-
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For reviews, see:
For papers on C(sp3)–H functionalization using visible-light photoredox catalysis via a reductive quenching cycle, see:
For papers on C(sp3)–H functionalization using visible light photoredox catalysis via an oxidative quenching cycle, see:
For representative papers on other visible light photocatalysis, see:
For selected reviews on C(sp3)–H bond functionalization, see:
For Pt, see:
For representative reviews and papers on the use of arylsulfonyl chlorides as aryl group resources, see: