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dc.contributor.authorKokatla, Hari Prasad-
dc.contributor.authorSagar, Ram-
dc.contributor.authorVankar, Yashwant D.-
dc.date.accessioned2025-10-16T07:18:48Z-
dc.date.available2025-10-16T07:18:48Z-
dc.date.issued2008-
dc.identifier.citation10.1016/j.tetlet.2008.05.112en_US
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/3355-
dc.descriptionNITWen_US
dc.description.abstractEfficient and convenient syntheses of (2S,3S)-safingol and its natural (2S,3R)-isomer have been developed from 3,4,6-tri-O-benzyl glycals. The key step is the one-pot reduction of an azide, saturation of the double bonds and debenzylation under catalytic hydrogenation.en_US
dc.language.isoenen_US
dc.publisherTetrahedron Lettersen_US
dc.subjectSphingolipiden_US
dc.subjectSafingolen_US
dc.subjectGlycalsen_US
dc.subjectWittig reactionen_US
dc.subjectCatalytic hydrogenationen_US
dc.titleStereoselective synthesis of safingol and its natural stereoisomer from D-glycalsen_US
dc.typeArticleen_US
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