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

Philip Robert Skaanderup, Robert Madsen

Research output: Contribution to journalJournal articleResearchpeer-review

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-closing olefin metathesis as the key steps.
Original languageEnglish
JournalChemical Communications
Volume12
Pages (from-to)1106-1107
ISSN1359-7345
Publication statusPublished - 2001

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