Diastereoselective synthesis of alpha-substituted-gamma-butyrolactones of nucleosides via [1,5]-C,H insertion reactions of alpha-diazomalonates of nucleosides

Citation
J. Lim et al., Diastereoselective synthesis of alpha-substituted-gamma-butyrolactones of nucleosides via [1,5]-C,H insertion reactions of alpha-diazomalonates of nucleosides, CHEM COMMUN, (7), 2000, pp. 553-554
Citations number
12
Categorie Soggetti
Chemistry
Journal title
CHEMICAL COMMUNICATIONS
ISSN journal
13597345 → ACNP
Issue
7
Year of publication
2000
Pages
553 - 554
Database
ISI
SICI code
1359-7345(2000):7<553:DSOAON>2.0.ZU;2-2
Abstract
Diastereoselective and regioselective [1,5]-C,H insertion reactions of 2'-d eoxy-3'-diazomalonate nucleosides afforded tau-butyrolactones of nucleoside s as chiral synthons for the preparation of 2'-C-branched nucleosides.