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dc.contributor.authorChandrasekhar, C-
dc.contributor.authorManju John-
dc.contributor.authorRavi S Lankalapalli-
dc.date.accessioned2013-09-28T04:21:27Z-
dc.date.available2013-09-28T04:21:27Z-
dc.date.issued2013-
dc.identifier.citationTetrahedron Letters 54(29):3810-3812;2013en_US
dc.identifier.urihttp://hdl.handle.net/123456789/629-
dc.description.abstractA convenient synthesis of 1,2-dihydropyridine (1,2-DHP) has been developed from dienaminodioate and an imine mediated by trifluoroacetic acid in a one-pot cascade synthesis. The advantages associated with this transformation include conditions that are metal-free, room temperature, undistilled solvent, and expeditious in excellent yields. The substrate scope has been demonstrated with various aromatic, heteroaromatic, unsaturated aldehydes, and anilines, benzylic amines in impressive yields.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectDienaminodioateen_US
dc.subject1,2-Dihydropyridine (1,2-DHP)en_US
dc.subjectImineen_US
dc.titleCascade synthesis of 1,2-dihydropyridine from dienaminodioate and an imine: a three-component approachen_US
dc.typeArticleen_US
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