Abstract
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.
Original language | English |
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Pages (from-to) | 687-696 |
Number of pages | 10 |
Journal | Chemical and Pharmaceutical Bulletin |
Volume | 65 |
Issue number | 7 |
DOIs | |
State | Published - 2017 |
Keywords
- Dihydroxylation
- Osmium tetroxide
- Sphingofungin E
- Stereoselectivity
- Total synthesis
ASJC Scopus subject areas
- General Chemistry
- Drug Discovery