Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/2744
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dc.contributor.authorAidhen, Indrapal Singh-
dc.contributor.authorSatyamurthi, N-
dc.date.accessioned2009-01-13T05:08:55Z-
dc.date.available2009-01-13T05:08:55Z-
dc.date.issued2008-12-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/2744-
dc.description1851-1857en_US
dc.description.abstractTwo carbon chain homolgation of enantiopure four carbon erythro configured iodo derivative 5 with N-methoxy-N-methyl-2-phenylsulfonylacetamide 6 affords for the first time a stable and storable precursor 3 of D-amicetose in the acyclic form, wherein the sensitive aldehyde is masked as a Weinreb amide. The differential protection in this acyclic derivative offers all the potential to exclusively arrive at the pyranose form of the target dideoxy-sugar.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCB Vol.47B(12) [December 2008]en_US
dc.subjectLactoneen_US
dc.subjectHomologationen_US
dc.subjectAmideen_US
dc.subjectDeoxysugaren_US
dc.titleSynthesis of a stable, storable and differentially protected acyclic precursor of D-amicetose and its conversion to 4-O-benzyl-protected D-amicetoseen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.47B(12) December 2008]

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