A Lewis acid dependent asymmetric Diels-Alder process in the cyclization of new chiral acrylamides with dienes
Diels-Alder cycloadditions of chiral acrylamides with cyclopentadiene proceed with high diastereofacial selectivity, giving either endo-R to endo-S products depending of the Lewis acid used.
- Publisher
- ROYAL SOC CHEMISTRY
- Issue Date
- 1999-06
- Language
- English
- Article Type
- Article
- Keywords
(S)-PROLINE BENZYL ESTER; N-ACYLOXAZOLIDINONE; AUXILIARIES; DIENOPHILES; 2-OXAZOLONE; INDUCTION; ADDITIONS; CAMPHOR
- Citation
CHEMICAL COMMUNICATIONS, pp.963 - 964
- ISSN
- 1359-7345
- Appears in Collection
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