SYNTHESIS OF 6-EPICASTANOSPERMINE AND 1,6-DIEPICASTANOSPERMINE FROM L-GULONOLACTONE AND SYNTHESIS OF L-6-EPICASTANOSPERMINE AND L-1,6-DIEPICASTANOSPERMINE FROM D-GULONOLACTONE
The syntheses of the natural product 6-epicastanospermine [(1S,6R,7R,8R,8aR)-1,6,7,8-tetrahydroxyoctahydroindolizine], isolated from Castanospermum australe, and of 1,6-diepicastanospermine [(1R,6R,7R,8R,8aR)-1,6,7,8-tetrahydroxyoctahydro-indolizine] from L-gulonolactone and the synthesis of the ena...
| Váldodahkkit: | , , , |
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| Materiálatiipa: | Journal article |
| Giella: | English |
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1988
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| _version_ | 1826290107952398336 |
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| author | Fleet, G Ramsden, N Molyneux, R Jacob, G |
| author_facet | Fleet, G Ramsden, N Molyneux, R Jacob, G |
| author_sort | Fleet, G |
| collection | OXFORD |
| description | The syntheses of the natural product 6-epicastanospermine [(1S,6R,7R,8R,8aR)-1,6,7,8-tetrahydroxyoctahydroindolizine], isolated from Castanospermum australe, and of 1,6-diepicastanospermine [(1R,6R,7R,8R,8aR)-1,6,7,8-tetrahydroxyoctahydro-indolizine] from L-gulonolactone and the synthesis of the enantiomers, L-6-epicastanospermine [(1R,6S,7S,8S,8aS)-1,6,7,8-tetrahydroxyoctahydroindolizine] and L-1,6-diepicastanospermine [(1S,6S,7S,8S,8aS)-1,6,7,8-tetrahydroxyoctahydro-indolizine] from D-gulonolactone are reported. © 1988. |
| first_indexed | 2024-03-07T02:39:08Z |
| format | Journal article |
| id | oxford-uuid:a9d6dc2f-a6cb-472b-95c7-7d5c1bd8c6e6 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T02:39:08Z |
| publishDate | 1988 |
| record_format | dspace |
| spelling | oxford-uuid:a9d6dc2f-a6cb-472b-95c7-7d5c1bd8c6e62022-03-27T03:10:58ZSYNTHESIS OF 6-EPICASTANOSPERMINE AND 1,6-DIEPICASTANOSPERMINE FROM L-GULONOLACTONE AND SYNTHESIS OF L-6-EPICASTANOSPERMINE AND L-1,6-DIEPICASTANOSPERMINE FROM D-GULONOLACTONEJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:a9d6dc2f-a6cb-472b-95c7-7d5c1bd8c6e6EnglishSymplectic Elements at Oxford1988Fleet, GRamsden, NMolyneux, RJacob, GThe syntheses of the natural product 6-epicastanospermine [(1S,6R,7R,8R,8aR)-1,6,7,8-tetrahydroxyoctahydroindolizine], isolated from Castanospermum australe, and of 1,6-diepicastanospermine [(1R,6R,7R,8R,8aR)-1,6,7,8-tetrahydroxyoctahydro-indolizine] from L-gulonolactone and the synthesis of the enantiomers, L-6-epicastanospermine [(1R,6S,7S,8S,8aS)-1,6,7,8-tetrahydroxyoctahydroindolizine] and L-1,6-diepicastanospermine [(1S,6S,7S,8S,8aS)-1,6,7,8-tetrahydroxyoctahydro-indolizine] from D-gulonolactone are reported. © 1988. |
| spellingShingle | Fleet, G Ramsden, N Molyneux, R Jacob, G SYNTHESIS OF 6-EPICASTANOSPERMINE AND 1,6-DIEPICASTANOSPERMINE FROM L-GULONOLACTONE AND SYNTHESIS OF L-6-EPICASTANOSPERMINE AND L-1,6-DIEPICASTANOSPERMINE FROM D-GULONOLACTONE |
| title | SYNTHESIS OF 6-EPICASTANOSPERMINE AND 1,6-DIEPICASTANOSPERMINE FROM L-GULONOLACTONE AND SYNTHESIS OF L-6-EPICASTANOSPERMINE AND L-1,6-DIEPICASTANOSPERMINE FROM D-GULONOLACTONE |
| title_full | SYNTHESIS OF 6-EPICASTANOSPERMINE AND 1,6-DIEPICASTANOSPERMINE FROM L-GULONOLACTONE AND SYNTHESIS OF L-6-EPICASTANOSPERMINE AND L-1,6-DIEPICASTANOSPERMINE FROM D-GULONOLACTONE |
| title_fullStr | SYNTHESIS OF 6-EPICASTANOSPERMINE AND 1,6-DIEPICASTANOSPERMINE FROM L-GULONOLACTONE AND SYNTHESIS OF L-6-EPICASTANOSPERMINE AND L-1,6-DIEPICASTANOSPERMINE FROM D-GULONOLACTONE |
| title_full_unstemmed | SYNTHESIS OF 6-EPICASTANOSPERMINE AND 1,6-DIEPICASTANOSPERMINE FROM L-GULONOLACTONE AND SYNTHESIS OF L-6-EPICASTANOSPERMINE AND L-1,6-DIEPICASTANOSPERMINE FROM D-GULONOLACTONE |
| title_short | SYNTHESIS OF 6-EPICASTANOSPERMINE AND 1,6-DIEPICASTANOSPERMINE FROM L-GULONOLACTONE AND SYNTHESIS OF L-6-EPICASTANOSPERMINE AND L-1,6-DIEPICASTANOSPERMINE FROM D-GULONOLACTONE |
| title_sort | synthesis of 6 epicastanospermine and 1 6 diepicastanospermine from l gulonolactone and synthesis of l 6 epicastanospermine and l 1 6 diepicastanospermine from d gulonolactone |
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