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dc.contributor.authorMajumdar, K C-
dc.contributor.authorDas, T K-
dc.contributor.authorChattopadhyay, B-
dc.date.accessioned2008-04-03T09:25:15Z-
dc.date.available2008-04-03T09:25:15Z-
dc.date.issued2007-08-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/690-
dc.description1337-1342en_US
dc.description.abstractThermal rearrangement of 6-[N-(4/-aryloxybut-2-ynyl)N-methylamino]coumarins in refluxing N,N-DEA has led to Claisen rearrangement at the aryloxypropargyl segment resulting in the formation of N-(4/-coumarinylmethyl),N-methylcoumarins in excellent yield.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCB Vol.46B(8) [August 2007]en_US
dc.subject6-Aminocoumarinen_US
dc.subjectClaisen rearrangementen_US
dc.subjectBenzopyranen_US
dc.subject1,4-dichlorobut-2-yneen_US
dc.subjectSigmatropic rearrangementen_US
dc.titleCompetitive [3,3] sigmatropic rearrangement of aryl propargyl ether moiety vs propargyl vinyl amine part in 6-[N-(4-aryloxybut-2-ynyl) N-methyl amino]coumarinsen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.46B(08) [August 2007]

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