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Nickel catalyzed multicomponent stereodivergent synthesis of olefins enabled by electrochemistry, photocatalysis and photo-electrochemistry

Chemistry

Nickel catalyzed multicomponent stereodivergent synthesis of olefins enabled by electrochemistry, photocatalysis and photo-electrochemistry

C. Zhu, H. Yue, et al.

Discover a groundbreaking three-component, reductive cascade reaction for arylalkylation of alkynes, developed by Chen Zhu, Huifeng Yue, and Magnus Rueping. This innovative approach yields a variety of trisubstituted alkenes with unparalleled chemo- and stereoselectivity, showcasing exclusive formation of *E* and *Z* isomers through distinct electrochemical and photocatalytic methods.

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Abstract
Trisubstituted alkenes are important organic synthons with broad applications in pharmaceuticals and materials. The stereoselective synthesis of such compounds remains challenging. Here, a three-component, reductive cascade cross-coupling for the arylalkylation of alkynes is reported. By switching between electrochemistry and photocatalysis, a wide range of trisubstituted alkenes are obtained in good to high yields with excellent chemo- and stereoselectivity. Under electrochemical nickel catalysis, the E isomer is obtained exclusively, while under photo/nickel dual catalysis the Z isomer is generated with high stereoselectivity. Moreover, a photo-assisted electrochemical nickel-catalyzed protocol selectively delivers Z-trisubstituted alkenes without added photocatalyst.
Publisher
Nature Communications
Published On
Jun 10, 2022
Authors
Chen Zhu, Huifeng Yue, Magnus Rueping
Tags
reductive cascade
cross-coupling reaction
arylalkylation
trisubstituted alkenes
electrochemistry
photocatalysis
nickel-catalyzed
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