Iodine-mediated intramolecular electrophilic aromatic cyclization in allylamines: A general route to synthesis of quinolines, pyrazolo[4,3-b]pyridines and thieno[3,2-b]pyridines§

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dc.contributor.author Batchu, Harikrishna
dc.contributor.author Bhattacharyya, Soumya
dc.contributor.author Batra, Sanjay
dc.date.accessioned 2013-09-05T11:29:18Z
dc.date.available 2013-09-05T11:29:18Z
dc.date.issued 2012
dc.identifier.citation Organic Letters, 2012, 14 (24), 6330–6333 en
dc.identifier.uri http://hdl.handle.net/123456789/1123
dc.description.abstract An unprecedented synthesis of aromatic ring annulated pyridines from suitably substituted primary allylamines via intramolecular electrophilic aromatic cyclization mediated by molecular iodine under mild conditions is described. en
dc.format.extent 486892 bytes
dc.format.mimetype application/pdf
dc.language.iso en en
dc.relation.ispartofseries 8368 en
dc.subject Iodine-mediated intramolecular en
dc.subject Quinolines en
dc.title Iodine-mediated intramolecular electrophilic aromatic cyclization in allylamines: A general route to synthesis of quinolines, pyrazolo[4,3-b]pyridines and thieno[3,2-b]pyridines§ en
dc.type Article en


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