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Cascade synthesis of 1,2-dihydropyridine from dienaminodioate and an imine: a three-component approach

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dc.contributor.author Chandrasekhar, C
dc.contributor.author Manju John
dc.contributor.author Ravi S Lankalapalli
dc.date.accessioned 2013-09-28T04:21:27Z
dc.date.available 2013-09-28T04:21:27Z
dc.date.issued 2013
dc.identifier.citation Tetrahedron Letters 54(29):3810-3812;2013 en_US
dc.identifier.uri http://hdl.handle.net/123456789/629
dc.description.abstract A 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.iso en en_US
dc.publisher Elsevier en_US
dc.subject Dienaminodioate en_US
dc.subject 1,2-Dihydropyridine (1,2-DHP) en_US
dc.subject Imine en_US
dc.title Cascade synthesis of 1,2-dihydropyridine from dienaminodioate and an imine: a three-component approach en_US
dc.type Article en_US


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