Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/8976
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dc.contributor.authorSengupta, Saumitra-
dc.contributor.authorMondal, Somnath-
dc.date.accessioned2010-05-14T11:36:04Z-
dc.date.available2010-05-14T11:36:04Z-
dc.date.issued2005-03-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/8976-
dc.description553-556en_US
dc.description.abstractA new stereoselective synthetic route to a -hydroxyalkyl-2-butenolide has been described starting from the -hydroxy acid chiral pool and via the intermediacy of an enantiopure -hydroxy--ketosulfone. A non-chelation controlled borohydride reduction (80% de) step is the key to the high diastereoselectivity observed in this synthesis.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 D 307/26en_US
dc.sourceIJC-B Vol.44B(03) [March 2005]en_US
dc.titleA chiral pool based synthetic strategy for -hydroxyalkyl-2-butenolidesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(03) [March 2005]

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