Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/4993
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dc.contributor.authorSingh, Gurdeep-
dc.contributor.authorSharma, Sonam-
dc.contributor.authorRekha-
dc.contributor.authorPandey, Rajat-
dc.contributor.authorSingh, Rupali-
dc.contributor.authorKumar, Tarunjeet-
dc.contributor.authorAnand, Ramasamy Vijaya-
dc.date.accessioned2023-08-21T16:10:41Z-
dc.date.available2023-08-21T16:10:41Z-
dc.date.issued2022-
dc.identifier.citationEuropean Journal of Organic Chemistry, 2022(32), 2200792.en_US
dc.identifier.urihttps://doi.org/10.1002/ejoc.202200792-
dc.identifier.urihttp://hdl.handle.net/123456789/4993-
dc.descriptionOnly IISER Mohali authors are available in the record.en_US
dc.description.abstractA one-pot approach for the synthesis of oxygen-containing heterocycles such as 4H-chromenes and 4H-chromen-4-ones has been established through the reaction of enaminones with p-quinone methides (p-QMs). This transformation basically involves an acid-catalyzed 1,6-conjugate addition of enaminones to p-QMs followed by annulation. In the case of reaction between 2-hydroxyphenyl-substituted p-quinone methides and N,N-dimethyl enaminones, 4H-chromene derivatives were obtained in moderate to excellent yields. Similarly, the reaction between simple p-quinone methides and 2-hydroxyphenyl-substituted N,N-dimethyl enaminones led to 4H-chromen-4-one derivatives in good yields.en_US
dc.language.isoen_USen_US
dc.publisherJohn Wiley & Sonsen_US
dc.subjectEnaminones with p-Quinone Methidesen_US
dc.subject4H-Chromeneen_US
dc.subject4H-Chromen-4-one Derivativesen_US
dc.titleReactions of Enaminones with p-Quinone Methides: Access to 4H-Chromene and 4H-Chromen-4-one Derivativesen_US
dc.typeArticleen_US
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