On the Way to Liposidomycins, New Nucleoside Antibiotics. Access to the Homochiral Diazepanone Core

Abstract
Access to the homochiral diazepanone core of liposidomycins has been carried out through the regiospecific nucleophilic opening of an enantiomerically pure α-amino-β,γ-epoxy-acid precursor, by an L-amino acid derivative, on one hand and cyclisation by a peptidic coupling reaction, on the other hand.

This publication has 17 references indexed in Scilit: