Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/6222
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dc.contributor.authorSingh, Sukhprit-
dc.contributor.authorMahajan, Vandana-
dc.date.accessioned2009-10-21T04:37:39Z-
dc.date.available2009-10-21T04:37:39Z-
dc.date.issued2006-02-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/6222-
dc.description561-563en_US
dc.description.abstractSelective oxidation of oligoethylene glycol ether methyl 12(13)–hydroxy-13(12)-[11-hydroxy-3,6,9-trioxa-undecyl-1-oxy]-octadec-9-enoate 3 has been studied using pyridinium chlorochromate (PCC). The reaction has resulted in the formation of methyl 12(13)–oxo-13(12)-[11-hydroxy-3,6,9-trioxa-undecyl-1-oxy]-octadec-9-enoate 5 as an unexpected product wherein only the secondary hydroxyl group has been oxidized while the primary hydroxyl group has remained intact.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 Cen_US
dc.sourceIJC-B Vol.45B(02) [February 2006]en_US
dc.subjectSelective oxidationen_US
dc.subjectpyridinium chloro chromate (PCC)en_US
dc.subjectvernolic aciden_US
dc.subjectVernonia anthelminticaen_US
dc.titleSelective oxidation of secondary over primary hydroxyl groupen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.45B(02) [February 2006]

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