Short syntheses of enantiopure calystegine B-2, B-3, and B-4

Authors
Skaanderup, PR Madsen, R
Citation
Pr. Skaanderup et R. Madsen, Short syntheses of enantiopure calystegine B-2, B-3, and B-4, CHEM COMMUN, (12), 2001, pp. 1106-1107
Citations number
18
Categorie Soggetti
Chemistry
Journal title
CHEMICAL COMMUNICATIONS
ISSN journal
13597345 → ACNP
Issue
12
Year of publication
2001
Pages
1106 - 1107
Database
ISI
SICI code
1359-7345(20010621):12<1106:SSOECB>2.0.ZU;2-8
Abstract
Calystegine B-2 B-3, and B-4 have been prepared in 5 steps from the benzyl protected methyl 6-iodoglycopyranosides of glucose, galactose and mannose, respectively, by using a zinc-mediated domino reaction followed by ring-clo sing olefin metathesis as the key steps.