Stereoselective free radical phenylsulfenylation of a nonactivated δ-carbon atom

A stereoselective free radical introduction of a phenylthio group onto a nonactivated methyl group in the δ-position, adjacent to a prochiral carbon atom, was achieved by photolysis of (-)-menthyl benzenesulfenate in the presence of hexabutylditin and (1R, 3R, 4S, 8S)-9-phenylthiomenthol (4) was obt...

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Bibliographic Details
Main Authors: Petrović Goran, Saičić Radomir N., Došen-Mićović Ljiljana I., Čeković Živorad
Format: Article
Language:English
Published: Serbian Chemical Society 2004-01-01
Series:Journal of the Serbian Chemical Society
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0352-5139/2004/0352-51390410737P.pdf