Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16572
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dc.contributor.authorNandanan, E-
dc.contributor.authorPhukan, Prodeep-
dc.contributor.authorSudalai, A-
dc.date.accessioned2013-03-29T11:13:15Z-
dc.date.available2013-03-29T11:13:15Z-
dc.date.issued1999-08-
dc.identifier.urihttp://hdl.handle.net/123456789/16572-
dc.description893-896en_US
dc.description.abstractThe synthesis of optically active β-hydroxy acids 5a-c is achieved in four steps from their corresponding terminal olefins 1a-c by employing Sharpless asymmetric dihydroxylation. The regioselective ring opening of chiral cyclic sulfites 3a-c with cyanide ion, constitutes the key reaction, thus producing the hydroxy nitriles 4a-c.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.38B(08) [August 1999]en_US
dc.titleAn efficient method to chiral β-hydroxy acids: Synthesis of lipid-A side chainen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.38B(08) [August 1999]

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