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 |
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| Format: | Journal article
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| Language: | English |
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| Published: |
1994
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