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dc.contributor.authorSINGH, AKen_US
dc.contributor.authorASEFA, Aen_US
dc.date.accessioned2011-08-30T17:57:50Zen_US
dc.date.accessioned2011-12-26T12:59:05Zen_US
dc.date.accessioned2011-12-27T05:50:01Z
dc.date.available2011-08-30T17:57:50Zen_US
dc.date.available2011-12-26T12:59:05Zen_US
dc.date.available2011-12-27T05:50:01Z
dc.date.issued2007en_US
dc.identifier.citationSYNTHETIC COMMUNICATIONS, 37(7-9), 1491-1494en_US
dc.identifier.issn0039-7911en_US
dc.identifier.urihttp://dx.doi.org/10.1080/00397910701229073en_US
dc.identifier.urihttp://dspace.library.iitb.ac.in/xmlui/handle/10054/12414en_US
dc.identifier.urihttp://hdl.handle.net/10054/12414
dc.description.abstractN-Ethyl-3-styrylindoles are prepared under modified Wittig-Horner reaction conditions.en_US
dc.language.isoenen_US
dc.publisherTAYLOR & FRANCIS INCen_US
dc.subjectCatalysisen_US
dc.subjectSalten_US
dc.subject.otherN-Alkylationen_US
dc.subject.other3-Styrylindoleen_US
dc.subject.otherWittig-Horner Reactionen_US
dc.titleN-alkylation of indole compounds in modified Wittig-Horner reactionen_US
dc.typeArticleen_US


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