Photoredox/Nickel Dual Catalysis for Regio- and Stereoselective Reductive Coupling of Alkynes with Vinyl Phosphonates

An efficient nickel-photoredox dual-catalyzed intermolecular reductive coupling reaction of alkynes with vinyl phosphonates is described. The reaction is highly regio- and stereoselective, affording the homoallylic phosphonates in good to high yields. The present protocol is also successfully applied to other activated alkenes such as enones, acrylates, and vinyl sulfone. The reaction is believed to proceed via the nickelacyclopentene intermediate. Mechanistic investigations, including control experiments and isotopic labeling studies, revealed that methanol serves as a proton source rather than a reducing agent.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-08-29
DOI
https://doi.org/10.1021/acs.joc.5c01619
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.94

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article

Photoredox/Nickel Dual Catalysis for Regio- and Stereoselective Reductive Coupling of Alkynes with Vinyl Phosphonates

Baburaj Baskar, Sabyasachi Chakrabortty, Dilip K. Sen Sharma, Subramaniyan Mannathan et al.
1 citations
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
0.94
article

Photoredox/Nickel Dual Catalysis for Regio- and Stereoselective Reductive Coupling of Alkynes with Vinyl Phosphonates

Baburaj Baskar, Sabyasachi Chakrabortty, Dilip K. Sen Sharma, Subramaniyan Mannathan, Rituparna Dutta, Radhakrishnan Sakthiganapathi
article en
1 citations

Abstract

An efficient nickel-photoredox dual-catalyzed intermolecular reductive coupling reaction of alkynes with vinyl phosphonates is described. The reaction is highly regio- and stereoselective, affording the homoallylic phosphonates in good to high yields. The present protocol is also successfully applied to other activated alkenes such as enones, acrylates, and vinyl sulfone. The reaction is believed to proceed via the nickelacyclopentene intermediate. Mechanistic investigations, including control experiments and isotopic labeling studies, revealed that methanol serves as a proton source rather than a reducing agent.

The Journal of Organic ChemistryVol. 90(36)
SRM Institute of Science and Technology (IN), SRM University (IN)
SRM Institute of Science and Technology, Department of Science and Technology, Ministry of Science and Technology, India
Openalex Percentile: Top 22%
Catalytic C–H Functionalization Methods
0.94
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