Abstract
The chirality transfer on the β-tetronic acid templates has been examined via highly diastereoselective alkylation or the Michael reaction at the α-position of the acids. Synthetic utility of this transfer procedure was demonstrated by the formal synthesis of (+)-cassiol and enantiodivergent synthesis of O-methyljoubertiamine.
Original language | English |
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Pages (from-to) | 1321-1343 |
Number of pages | 23 |
Journal | Heterocycles |
Volume | 51 |
Issue number | 6 |
DOIs | |
State | Published - 1999/06/01 |
ASJC Scopus subject areas
- Analytical Chemistry
- Pharmacology
- Organic Chemistry