Abstract
Reaction of camphor N-enoylpyrazolidinones (1a-j) with various oxidants, in particular UHP/TFAA afford chiral epoxides with a wide range of stereoselectivities (up to > 90% de).
Original language | English |
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Pages (from-to) | 1047-1051 |
Number of pages | 5 |
Journal | Journal of the Chinese Chemical Society |
Volume | 50 |
Issue number | 5 |
DOIs | |
Publication status | Published - 2003 |
Keywords
- Asymmetric
- Camphor
- Chiral auxiliary
- Diastereoselectivity
- Epoxide
- Lewis acid
- Mechanism
- Stereoinduction
ASJC Scopus subject areas
- General Chemistry