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Nickel catalyzed multicomponent stereodivergent synthesis of olefins enabled by electrochemistry, photocatalysis and photo-electrochemistry
Trisubstituted alkenes are important organic synthons and have broad applications in the synthesis of many pharmaceuticals and materials. The stereoselective synthesis of such compounds has long been a research focus for organic researchers. Herein, we report a three-component, reductive cascade, cr...
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Published in: | Nature communications 2022-06, Vol.13 (1), p.3240-3240, Article 3240 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Trisubstituted alkenes are important organic synthons and have broad applications in the synthesis of many pharmaceuticals and materials. The stereoselective synthesis of such compounds has long been a research focus for organic researchers. Herein, we report a three-component, reductive cascade, cross-coupling reaction for the arylalkylation of alkynes. A wide range of trisubstituted alkenes are obtained in good to high yields with excellent chemo- and stereoselectivity by switching between electrochemistry and photocatalysis. The
E
isomer of the product is obtained exclusively when the reaction is conducted with electricity and nickel, while the
Z
isomer is generated with high stereoselectivity when photo- and nickel dual catalysts are used. Moreover, photo-assisted electrochemically enabled nickel catalyzed protocol is demonstrated to selectively deliver
Z
-trisubstituted alkenes without the addition of photocatalysts.
The construction of trisubstituted alkenes with high stereoselectivity is challenging. Here, the authors realize the stereodivergent synthesis of such compounds via switching between electrochemistry, photochemistry and photoelectrochemistry. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-022-30985-2 |