Enantiomerically pure a-Li alkyl-sulfoxides can be used as chiral cl-chloroalkyl carbanions with N-protected imines by means of the 'non-oxidative' chloro-Pummerer reaction (NOCPR). This novel methodology allows for a one-pot displacement of a sulfinyl group by chlorine from N-alkoxycarbonyl beta -sulfinylamines derived from aryl, fluoroalkyl and alkyl imines, with clean stereoinversion at carbon. Several 1,2-chloroamines produced via NOCPR were transformed into the corresponding aziridines. (C) 2001 Elsevier Science Ltd. All rights reserved.
Synthesis of (+)- and (−)-Statine via Chiral Sulfoxide Chemistry
作者:Cristina Pesenti、Pierfrancesco Bravo、Eleonora Corradi、Massimo Frigerio、Stefano V. Meille、Walter Panzeri、Fiorenza Viani、Matteo Zanda