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dc.contributor.authorBASKARAN, Sen_US
dc.contributor.authorBAIG, MHAen_US
dc.contributor.authorBANERJEE, Sen_US
dc.contributor.authorBASKARAN, Cen_US
dc.contributor.authorBHANU, Ken_US
dc.contributor.authorDESHPANDE, SPen_US
dc.contributor.authorTRIVEDI, GKen_US
dc.date.accessioned2011-08-23T11:42:50Zen_US
dc.date.accessioned2011-12-26T12:56:26Zen_US
dc.date.accessioned2011-12-27T05:45:10Z
dc.date.available2011-08-23T11:42:50Zen_US
dc.date.available2011-12-26T12:56:26Zen_US
dc.date.available2011-12-27T05:45:10Z
dc.date.issued1996en_US
dc.identifier.citationTETRAHEDRON, 52(18), 6437-6452en_US
dc.identifier.issn0040-4020en_US
dc.identifier.urihttp://dx.doi.org/10.1016/0040-4020(96)00278-5en_US
dc.identifier.urihttp://dspace.library.iitb.ac.in/xmlui/handle/10054/10504en_US
dc.identifier.urihttp://hdl.handle.net/10054/10504
dc.description.abstractReproducible. high-yielding, cost efficient regio-and stereoselective synthesis of the title compound 3 isolated from Shark Liver Oil has been described. The compound 3 is prepared in an overall yield of 41% from chiral synthon 4 by the sequential reaction of 4 with C-13 Wittig salt: hydrogenation: epoxidation and regioselective opening. The oxo analogs 18 and 19 are prepared from four different achiral synthons by the sequential regioselective opening of the corresponding epoxide with different alcohols. methylation and deprotection strategies.en_US
dc.language.isoenen_US
dc.publisherPERGAMON-ELSEVIER SCIENCE LTDen_US
dc.titleAn efficient and stereoselective synthesis of (2R,2'S)-1-O-(2'-hydroxy-hexadecyl)glycerol and its oxo analogs: Potential antitumour compounds from shark liver oil.en_US
dc.typeArticleen_US


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