SYNTHESIS OF THE C1-C8 TETRAHYDROPYRANYL SEGMENT OF THE ANTIFUNGAL AGENT AMBRUTICIN AND ITS C3 EPIMER

Authors
LIU LP DONALDSON WA
Citation
Lp. Liu et Wa. Donaldson, SYNTHESIS OF THE C1-C8 TETRAHYDROPYRANYL SEGMENT OF THE ANTIFUNGAL AGENT AMBRUTICIN AND ITS C3 EPIMER, Synlett, (1), 1996, pp. 103-104
Citations number
10
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synlett → ACNP
ISSN journal
09365214
Issue
1
Year of publication
1996
Pages
103 - 104
Database
ISI
SICI code
0936-5214(1996):1<103:SOTCTS>2.0.ZU;2-P
Abstract
The synthesis of the C1-C8 segment (2) of ambruticin and its C3 epimer (9), were accomplished starting from the diethyldithioacetal of L-ara binose in 10 and 8 steps (10% and 16% yield) respectively.