ALDOL EQUILIBRATIONS OF UNPROTECTED TRIHYDROXYBICYCLIC LACTONES - ENANTIOMERIC TETRAHYDROXY-ALPHA-AMINOCYCLOPENTANE CARBOXYLIC-ACIDS FROM EPIMERIC BICYCLIC LACTONES

Six stereoisomers - including an enantiomeric pair - of 1-amino-2,3,4,5-tetrahydroxy-cyclopentane-1-carboxylate have been prepared from a single azidolactone starting material by a series of remarkable aldol equilibrations. © 1994.

Bibliographic Details
Main Authors:	Hui, A, Fairbanks, A, Nash, R, Lilley, P, Storer, R, Watkin, D, Fleet, G
Format:	Journal article
Language:	English
Published:	1994

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