Radical cyclization of oxime ethers derived from monosaccharides aiming atthe synthesis of dysiherbaine and related stereoisomers

Authors
Naito, T Nair, JS Nishiki, A Yamashita, K Kiguchi, T
Citation
T. Naito et al., Radical cyclization of oxime ethers derived from monosaccharides aiming atthe synthesis of dysiherbaine and related stereoisomers, HETEROCYCLE, 53(12), 2000, pp. 2611
Citations number
15
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
HETEROCYCLES
ISSN journal
03855414 → ACNP
Volume
53
Issue
12
Year of publication
2000
Database
ISI
SICI code
0385-5414(200012)53:12<2611:RCOOED>2.0.ZU;2-2
Abstract
Stannyl radical-mediated cyclization of oxime ethers (6), (14), (22), and ( 29) derived from glucose and galactose afforded the cyclized aminosugar der ivatives (7), (8), (15, 16 and 17), (23), (24), and (30, 31 and 32) which w ould serve as key intermediates for the synthesis of dysiherbaine and its i somers.