First synthesis of allyl isonitriles from Baylis-Hillman adducts and their syn-thetic application for obtaining substituted imidazo[1,2-a]pyridine and dibenzoazulene systems

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dc.contributor.author Nayak, Maloy
dc.contributor.author Kanojiya, Sanjeev
dc.contributor.author Batra, Sanjay
dc.date.accessioned 2010-03-03T09:54:23Z
dc.date.available 2010-03-03T09:54:23Z
dc.date.issued 2009
dc.identifier.citation Synthesis 2009, No.3, 431-437 en
dc.identifier.uri http://hdl.handle.net/123456789/522
dc.description.abstract First report of stereoselective synthesis of substituted allyl isonitriles from the primary allyl amines generated from the Baylis-Hillman adduct and its utilization in a robust IMCR to afford substituted imidazo[1,2-a]pyridine in the presence of NH4Cl is described en
dc.format.extent 139579 bytes
dc.format.mimetype application/pdf
dc.language.iso en en
dc.relation.ispartofseries CDRI Communication Number 7599 en
dc.subject Isonitrile en
dc.subject Baylis-Hillman en
dc.subject allyl amine en
dc.subject MCR en
dc.subject imidazo[2,1-a]pyridine en
dc.title First synthesis of allyl isonitriles from Baylis-Hillman adducts and their syn-thetic application for obtaining substituted imidazo[1,2-a]pyridine and dibenzoazulene systems en
dc.type Article en


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