Abstract
The first nucleophilic substitution reaction of organoindium with sulfonyl chlorides has been exploited. This reaction of vinylindium, derived from terminal alkynes via hydroindation, with sulfonyl chlorides in the presence of Ag 2O provides access to vinyl sulfones. The vinyl sulfones were formed highly regio-and stereo-selectively with E stereochemistry. © ARKAT USA, Inc.
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CITATION STYLE
Deng, G., & Zou, J. (2010). The first nucleophilic substitution reaction of organoindium reagents with sulfonyl chlorides: A facile method for preparation of vinyl sulfones. Arkivoc, 2010(2), 186–194. https://doi.org/10.3998/ark.5550190.0011.214
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