Photoredox/nickel dual-catalyzed regio- and stereo-selective cross-coupling of allyl trifluoroborates with alkenyl electrophiles: synthesis of 1,4-dienes

A mild photoredox/Ni dual-catalyzed cross-coupling of allyl trifluoroborates with vinyl bromides or triflates enables efficient synthesis of 1,4-dienes with high regio- and stereo-selectivity, broad substrate scope and functional group tolerance.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00317b
Citations
1
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.79
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article

Photoredox/nickel dual-catalyzed regio- and stereo-selective cross-coupling of allyl trifluoroborates with alkenyl electrophiles: synthesis of 1,4-dienes

Yuanhong Liu, Peizhuo Lv, Xin Xie
1 citations
Organic Chemistry Frontiers
Fluorine in Organic Chemistry
0.79
article

Photoredox/nickel dual-catalyzed regio- and stereo-selective cross-coupling of allyl trifluoroborates with alkenyl electrophiles: synthesis of 1,4-dienes

Yuanhong Liu, Peizhuo Lv, Xin Xie
article en
1 citations

Abstract

A mild photoredox/Ni dual-catalyzed cross-coupling of allyl trifluoroborates with vinyl bromides or triflates enables efficient synthesis of 1,4-dienes with high regio- and stereo-selectivity, broad substrate scope and functional group tolerance.

Organic Chemistry FrontiersVol. 12(15)
Chinese Academy of Sciences (CN), Shanghai Institute of Organic Chemistry (CN)
Openalex Percentile: Top 29%
Fluorine in Organic Chemistry
0.79
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