Realisation of highly stereoselective dihydroxylation of a cyclopentene inthe synthesis of (-)-aristeromycin

Authors
Tokoro, Y Kobayashi, Y
Citation
Y. Tokoro et Y. Kobayashi, Realisation of highly stereoselective dihydroxylation of a cyclopentene inthe synthesis of (-)-aristeromycin, CHEM COMMUN, (9), 1999, pp. 807-808
Citations number
33
Categorie Soggetti
Chemistry
Journal title
CHEMICAL COMMUNICATIONS
ISSN journal
13597345 → ACNP
Issue
9
Year of publication
1999
Pages
807 - 808
Database
ISI
SICI code
1359-7345(19990507):9<807:ROHSDO>2.0.ZU;2-H
Abstract
A 2-furyl group was used as a synthetic equivalent of the CH2OH at the 4' p osition of aristeromycin, and dihydroxylation of the cyclopentene possessin g the furyl group proceeded highly stereoselectively to produce the key dio l for the synthesis of (-)-aristeromycin.