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dc.contributor.authorAshitha, K T-
dc.contributor.authorPraveen Kumar, V-
dc.contributor.authorFathimath Salfeena, C T-
dc.contributor.authorSasidhar, B S-
dc.date.accessioned2018-02-02T15:58:11Z-
dc.date.available2018-02-02T15:58:11Z-
dc.date.issued2018-01-05-
dc.identifier.citationThe Journal of Organic Chemistry, 83(1):113-124en_US
dc.identifier.urihttp://10.10.100.66:8080/xmlui/handle/123456789/2987-
dc.description.abstractA simple and efficient one-pot annulation of arylidenones, alkynes, and nitriles in the presence of BF3·OEt2 is described. A highly functionalized variety of N-substituted pyridine-fused chromeno and pyrano derivatives were obtained with satisfactory yields under mild reaction conditions. The method was proven to be valid for the synthesis of a diverse library of chromeno[3,4-c]pyridines, thiochromeno[3,4-c]pyridines, pyrano[3,4-c]pyridines, and thiopyrano[3,4-c]pyridine derivatives from readily accessible substrates. This experimentally simple protocol provides structurally complex, biologically relevant heterocycles in a one-pot operation.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.titleBF3·OEt2‑Mediated Tandem Annulation: A Strategy To Construct Functionalized Chromeno- and Pyrano-Fused Pyridinesen_US
dc.typeArticleen_US
Appears in Collections:2018

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