Synthesis of the C1-C8 Tetrahydropyranyl Segment of the Antifungal Agent Ambruticin and its C3 Epimer

Authors

Luping Liu, Marquette UniversityFollow
William Donaldson, Marquette UniversityFollow

Document Type

Article

Language

eng

Publication Date

1996

Publisher

Thieme

Source Publication

Sunlett

Source ISSN

0936-5214

Abstract

The synthesis of the C1-C8 segment (2) of ambruticin and its C3 epimer (9), were accomplished starting from the diethyldithioacetal of L-arabinose in 10 and 8 steps (10% and 16% yield) respectively.

Comments

Synlett, Vol. 1 (1996): 103-104. DOI.

Recommended Citation

Liu, Luping and Donaldson, William, "Synthesis of the C1-C8 Tetrahydropyranyl Segment of the Antifungal Agent Ambruticin and its C3 Epimer" (1996). Chemistry Faculty Research and Publications. 865.
https://epublications.marquette.edu/chem_fac/865