ACCESS TO ENANTIOPURE RIBOSYL-DIAZEPANONE CORE OF LIPOSIDOMYCINS

Authors
LEMERRER Y GRAVIERPELLETIER C GERROUACHE M DEPEZAY JC
Citation
Y. Lemerrer et al., ACCESS TO ENANTIOPURE RIBOSYL-DIAZEPANONE CORE OF LIPOSIDOMYCINS, Tetrahedron letters, 39(5-6), 1998, pp. 385-388
Citations number
18
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
39
Issue
5-6
Year of publication
1998
Pages
385 - 388
Database
ISI
SICI code
0040-4039(1998)39:5-6<385:ATERCO>2.0.ZU;2-6
Abstract
A convergent synthesis of the ribosyl-diazepanone core of liposidomyci ns, new nucleoside antibiotics, has been carried out via enantiomerica lly pure epoxide and alpha-ribosyl aminoacid, chiral key intermediates obtained from L-ascorbic acid and D-ribose, respectively. (C) 1997 Pu blished by Elsevier Science Ltd. All rights reserved.