Interrupted Michael\nReaction: Sulfophosphinoylation\nof α,β-Unsaturated Ketones Catalyzed by Phosphine

An efficient method for phosphine-catalyzed sulfophosphinoylation\nof α,β-unsaturated ketones for synthesis allylic organophosphorus\ncompounds has been reported, in which α,β-unsaturated\ncompounds acting as zwitterions react with electrophiles and nucleophiles\nto form a C–P bond and a C–O bond and obtain allylic\norganophosphorus with high regio- and stereoselectivity in moderate\nto excellent yields.

Publication Details

Journal
Figshare
Published
2024-10-31
DOI
https://doi.org/10.1021/acs.joc.4c01860.s001
Primary Topic
Ion Channels and Receptors
Type
article
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article

Interrupted Michael\nReaction: Sulfophosphinoylation\nof α,β-Unsaturated Ketones Catalyzed by Phosphine

Figshare
Ion Channels and Receptors
article

Interrupted Michael\nReaction: Sulfophosphinoylation\nof α,β-Unsaturated Ketones Catalyzed by Phosphine

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Abstract

An efficient method for phosphine-catalyzed sulfophosphinoylation\nof α,β-unsaturated ketones for synthesis allylic organophosphorus\ncompounds has been reported, in which α,β-unsaturated\ncompounds acting as zwitterions react with electrophiles and nucleophiles\nto form a C–P bond and a C–O bond and obtain allylic\norganophosphorus with high regio- and stereoselectivity in moderate\nto excellent yields.

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Openalex Percentile: Top 56%
Ion Channels and Receptors
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Interrupted Michael\nReaction: Sulfophosphinoylation\nof α,β-Unsaturated Ketones Catalyzed by Phosphine · Figshare (2024) | TGRS Research Map | TGRS