Abstract
All four diastereomere of chiral alcohol 2 with three contiguous chiral centers were stereoselectively prepared via diastereoselective addition of nucleophiles (crotyl metal or H-) to α-methyl-β,γ-unsaturated carbonyl compounds 1.
Original language | English |
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Pages (from-to) | 3707-3710 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 26 |
Issue number | 31 |
DOIs | |
Publication status | Published - Jan 1 1985 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Organic Chemistry
- Drug Discovery