Asymmetric synthesis of a new proline analogue
- 1 January 1981
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 3,p. 97-98
- https://doi.org/10.1039/c39810000097
Abstract
The 1,3-dipolar cycloaddition to ethylene of N-glycosylnitrones, formed in situ from the partially protected d-mannose- or d-ribose-oximes and various glyoxalates, gave compounds which could be transformed into both enantiomers of 3-t-butoxycarbonyl-isoxazolidine and derivatives thereof.Keywords
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