Photoredox/Cobalt Cooperative Catalysis for Cycloisomerization of 1,6-Enynes

Under visible-light photocatalysis facilitated by cobalt coordination, a highly regio- and stereoselective cycloisomerization reaction of 1,6-enynes has been developed. This method enables the efficient synthesis of various skipped 1,4-diene products with excellent stereoselectivity, using commercially available cobalt catalysts, ligands, and reagents. Notably, the reaction exhibits remarkable regioselectivity (>20:1), stereoselectivity (<i>Z</i>/<i>E</i> > 20:1), and high yields (58-92%) under mild conditions, along with a broad substrate scope and good functional group tolerance.

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Publication Details

Journal
Organic Letters
Published
2025-09-10
DOI
https://doi.org/10.1021/acs.orglett.5c03418
Citations
2
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.87
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article

Photoredox/Cobalt Cooperative Catalysis for Cycloisomerization of 1,6-Enynes

Yang’en You, Zhiwei Jiang, Zhongjian Du, Chenlei Ji
2 citations
Organic Letters
Catalytic C–H Functionalization Methods
1.87
article

Photoredox/Cobalt Cooperative Catalysis for Cycloisomerization of 1,6-Enynes

Yang’en You, Zhiwei Jiang, Zhongjian Du, Chenlei Ji
article en
2 citations

Abstract

Under visible-light photocatalysis facilitated by cobalt coordination, a highly regio- and stereoselective cycloisomerization reaction of 1,6-enynes has been developed. This method enables the efficient synthesis of various skipped 1,4-diene products with excellent stereoselectivity, using commercially available cobalt catalysts, ligands, and reagents. Notably, the reaction exhibits remarkable regioselectivity (>20:1), stereoselectivity (<i>Z</i>/<i>E</i> > 20:1), and high yields (58-92%) under mild conditions, along with a broad substrate scope and good functional group tolerance.

Organic LettersVol. 27(37)
Hefei University of Technology (CN)
Openalex Percentile: Top 14%
Catalytic C–H Functionalization Methods
1.87
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