Journal
CHEMICAL & PHARMACEUTICAL BULLETIN
Volume 65, Issue 7, Pages 687-696Publisher
PHARMACEUTICAL SOC JAPAN
DOI: 10.1248/cpb.c17-00322
Keywords
sphingofungin E; dihydroxylation; stereoselectivity; osmium tetroxide; total synthesis
Funding
- Japan Society for the Promotion of Science (JSPS) [JP16K08158]
- JSPS Core-to-Core Program, B. Asia-Africa Science Platforms
- Grants-in-Aid for Scientific Research [16K08158] Funding Source: KAKEN
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Total synthesis of sphingofungin E and 4,5-di-epi-sphingofungin E was achieved from an intermediate same as that of myriocin and mycestericin D via antipodal stereoselective dihydroxylations.
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