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.
| Main Authors: | , , , , , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
1994
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