Abstract
The dianion of the acetoacetic ester reacts with epibromohydrin derivatives to afford a mixture of (Z)-2-alkoxycarbonylmethylidenetetrahydrofuran derivative and (E)-2-alkoxycarbonylmethylidenetetrahydropyran derivative. The selective formation of the tetrahydrofuran derivative is achieved by the use of LiCIO4 as the additive. The preparation of the optically active tetrahydrofuran derivatives and tetrahydropyran derivatives is also examined, and the optical purity and absolute configuration of the products is elucidated.
Original language | English |
---|---|
Pages (from-to) | 1581-1585 |
Number of pages | 5 |
Journal | Chemical and Pharmaceutical Bulletin |
Volume | 48 |
Issue number | 10 |
DOIs | |
Publication status | Published - 2000 |
Keywords
- Acetoacetic ester
- Dianion
- Epibromohydrin
- Epoxide
- Tetrahydrofuran
- Tetrahydropyran
ASJC Scopus subject areas
- Chemistry(all)
- Drug Discovery