Abstract
Vanadium catalysts bearing (+)-ketopinic acid-based chiral hydroxamic acids as constituent ligands are investigated in the asymmetric epoxidation of allylic alcohols. Chiral ligands lacking an N-substituent and those having a bulkier aryl group in the bornane skeleton provided better selectivity.
Original language | English |
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Pages (from-to) | 2625-2628 |
Number of pages | 4 |
Journal | Tetrahedron Asymmetry |
Volume | 13 |
Issue number | 24 |
DOIs | |
Publication status | Published - 2002 Dec 9 |
Externally published | Yes |
ASJC Scopus subject areas
- Catalysis
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry