Stereoselective synthesis of 1,4-dideoxy-1,4-imino-L-lyxitol and 1,5-dideoxy-1,5-imino-D-ribitol

Authors
Jang, KC Jeong, IY Yang, MS Choi, SU Park, KH
Citation
Kc. Jang et al., Stereoselective synthesis of 1,4-dideoxy-1,4-imino-L-lyxitol and 1,5-dideoxy-1,5-imino-D-ribitol, HETEROCYCLE, 53(4), 2000, pp. 887-896
Citations number
27
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
HETEROCYCLES
ISSN journal
03855414 → ACNP
Volume
53
Issue
4
Year of publication
2000
Pages
887 - 896
Database
ISI
SICI code
0385-5414(20000401)53:4<887:SSO1A1>2.0.ZU;2-#
Abstract
1,4-Dideoxy-1,4-imino-L-lyxitol (2) and 1,5-dideoxy-1,5-imino-D-ribitol (3) were prepared from allylic alcohol (1) derived from D-glucono-delta-lacton e. Key transformation includes diastereoselective epoxidation of (1) with m -CPBA.