Journal of the Chemical Society. Chemical communications p. 97 - 98 (1981)
Update date:2022-08-12
Topics:
Vasella, Andrea
Voeffray, Robert
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.
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