Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/8983
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dc.contributor.authorSrikrishna, A-
dc.contributor.authorRamachary, D B-
dc.date.accessioned2010-05-14T11:41:09Z-
dc.date.available2010-05-14T11:41:09Z-
dc.date.issued2005-04-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/8983-
dc.description751-761en_US
dc.description.abstractSynthetic approach to 3-alkoxythapsane, comprising of the carbon framework of a small group of sesquiterpenes containing three contiguous quaternary carbon atoms has been described. A combination of alkylation, orthoester Claisen rearrangement and intramolecular diazoketone cyclopropanation has been employed for the creation of the three requisite contiguous quaternary carbon atoms.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 C 13/10en_US
dc.sourceIJC-B Vol.44B(04) [April 2005]en_US
dc.titleApproaches to sesquiterpenes containing three contiguous quaternary carbon atoms. Synthesis of 3-methoxythapseneen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(04) [April 2005]

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