Journal article
Synthesis of the enantiomers of 6-epicastanospermine and 1,6-diepicastanospermine from D- and L-gulonolactone.
- Abstract:
- The synthesis of the enantiomers of 6-epicastanospermine and of 1,6-diepicastanospermine from the enantiomeric gulonolactones is reported and the structure of the former is established as (1S,6R,7R,8R,8aR)-1,6,7,8-tetrahydroxyoctahydroindolizine. The inhibitory activities of the diastereomers against the amyloglucosidase-catalysed hydrolysis of p-nitrophenyl alpha-D-glucopyranoside were investigated, and the effects of 6-epicastanospermine and of 1,6-diepicastanospermine on 14 human liver glycosidases are reported.
- Publication status:
- Published
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- Publisher copy:
- 10.1016/0008-6215(90)80146-t
Authors
- Journal:
- Carbohydrate research More from this journal
- Volume:
- 205
- Issue:
- C
- Pages:
- 269-282
- Publication date:
- 1990-09-01
- DOI:
- EISSN:
-
1873-426X
- ISSN:
-
0008-6215
- Language:
-
English
- Keywords:
- Pubs id:
-
pubs:43469
- UUID:
-
uuid:0d5b431a-6897-47f4-9de6-4d5e542f6694
- Local pid:
-
pubs:43469
- Source identifiers:
-
43469
- Deposit date:
-
2012-12-19
- ARK identifier:
Terms of use
- Copyright date:
- 1990
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