A Convenient Method for the Preparation of Enantiomerically Pure 2-SubstitutedN-Tosylaziridines

Abstract
A three-step procedure for the synthesis of enantiomerically pure 2-substituted N-tosylaziridines 4 is described. The method involves N-tosylation of (S)-2-amino acids 1, followed by reduction to give N-tosyl-2-amino alcohols 3 and O-tosylation with in situ aziridine ring closure.

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