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A Cascade reaction actuated by Nucleophilic heterocyclic carbene catalyzed intramolecular addition of enals via homoenolate to r,β-unsaturated esters: Efficient synthesis of coumarin derivatives.

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dc.contributor.author Sinu, C R
dc.contributor.author Padmaja, D V M
dc.contributor.author Ranjini, U P
dc.contributor.author Seetha Lakshmi, K C
dc.contributor.author Suresh, E
dc.contributor.author Vijay Nair, G
dc.date.accessioned 2013-08-19T07:14:29Z
dc.date.available 2013-08-19T07:14:29Z
dc.date.issued 2013
dc.identifier.citation Organic Letters 15(1):68-71;4 Jan 2013 en_US
dc.identifier.uri http://hdl.handle.net/123456789/581
dc.description.abstract A nucleophilic heterocyclic carbene mediated intramolecular homoenolate reaction strategy for the efficient synthesis of 4-alkyl substituted coumarins is described. en_US
dc.language.iso en en_US
dc.publisher American Chemical Society en_US
dc.subject Activated double-bonds en_US
dc.subject Diels-Alder reactions en_US
dc.subject Stereoselective-synthesis en_US
dc.subject Gamma-butyrolactones en_US
dc.subject Stetter reaction en_US
dc.subject Formoin reaction en_US
dc.title A Cascade reaction actuated by Nucleophilic heterocyclic carbene catalyzed intramolecular addition of enals via homoenolate to r,β-unsaturated esters: Efficient synthesis of coumarin derivatives. en_US
dc.type Article en_US


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