- Abstract:
- Efficient but reversible aldol condensations of 2-azido-5-formyl-1,5-lactones provide short routes to precursors for α-cyclopentane amino acids, some aminopseudosugars and spirohydantoins of cyclopentanes with control of the stereochemistry at all 5 carbons bearing functional groups. The effects of some of the compounds on human liver-glycosidases are described. © 1993.
- Publication status:
- Published
- Publisher copy:
- 10.1016/S0040-4039(00)61521-6
-
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- Journal:
- TETRAHEDRON LETTERS
- Volume:
- 34
- Issue:
- 49
- Pages:
- 7953-7956
- Publication date:
- 1993-12-03
- DOI:
- ISSN:
-
0040-4039
- URN:
-
uuid:0e00d0fc-4bba-4ffb-b6ea-dad6ecb0ac38
- Source identifiers:
-
44375
- Local pid:
- pubs:44375
- Language:
- English
- Copyright date:
- 1993
Journal article
SYNTHESIS OF CYCLOPENTANE SPIROHYDANTOINS BY ALDOL CYCLIZATIONS - AN APPROACH TO HIGHLY SUBSTITUTED ALPHA-CYCLOPENTANE AMINO-ACIDS
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