CONCISE SYNTHESIS OF DEACETYLANISOMYCIN AND 2-SUBSTITUTED ANALOGS FROM N,2-O-DIBENZYL-1-THREOSE IMINE

Citation
U. Veith et al., CONCISE SYNTHESIS OF DEACETYLANISOMYCIN AND 2-SUBSTITUTED ANALOGS FROM N,2-O-DIBENZYL-1-THREOSE IMINE, Synlett, (12), 1996, pp. 1181
Citations number
64
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
09365214
Issue
12
Year of publication
1996
Database
ISI
SICI code
0936-5214(1996):12<1181:CSODA2>2.0.ZU;2-L
Abstract
Anisomycin derivatives like deacetylanisomycin 8k and 2-substituted an alogues have been prepared using a highly threo-selective addition of organolithium and Grignard compounds to N,2-O-dibenzyl-L-threose imine acetonide 4 and subsequent cyclization as key steps.