Abstract
Chiral trans-enals derived from 2-deoxypyranoses by ylide-induced β-elimination were exploited for the synthesis and stereochemical revision of a novel, marine eicosanoid.
Original language | English (US) |
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Pages (from-to) | 2971-2974 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 31 |
Issue number | 21 |
DOIs | |
State | Published - 1990 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry