Abstract
Both C(10) diastereomers of trioxilin B3, presumed to be a mixture of 10(R/S), 11(R), 12(R)-trihydroxyeicosa-5(Z), 8(Z), 14(Z)-trienoic acids, were prepared from a carbohydrate derived precursor by Wittig homologation and Mitsunobu inversion.
Original language | English (US) |
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Pages (from-to) | 4237-4240 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 29 |
Issue number | 34 |
DOIs | |
State | Published - 1988 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry