AN EXPEDITIOUS ROUTE TO CARBOCYCLIC NUCLEOSIDES - (-)-ARISTEROMYCIN AND (-)-CARBODINE

Authors
BURLINA F FAVRE A FOURREY JL THOMAS M
Citation
F. Burlina et al., AN EXPEDITIOUS ROUTE TO CARBOCYCLIC NUCLEOSIDES - (-)-ARISTEROMYCIN AND (-)-CARBODINE, Bioorganic & medicinal chemistry letters, 7(3), 1997, pp. 247-250
Citations number
31
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Medicinal
Journal title
Bioorganic & medicinal chemistry letters → ACNP
ISSN journal
0960894X
Volume
7
Issue
3
Year of publication
1997
Pages
247 - 250
Database
ISI
SICI code
0960-894X(1997)7:3<247:AERTCN>2.0.ZU;2-M
Abstract
The readily available bicyclic lactone (-)-1 was transformed into diac etate (-)-2 which served in an expeditious route to (-)-aristeromycin (3a) and (-)-carbodine (3b) in acceptable yields. (C) 1997, Elsevier S cience Ltd.