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Copper(II)-Catalyzed Synthesis of Pyrrolo[3,4-b]quinolinediones from o-Amino Carbonyl Compounds and Maleimides

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dc.contributor.author Kumar, Anil
dc.date.accessioned 2024-09-10T09:21:13Z
dc.date.available 2024-09-10T09:21:13Z
dc.date.issued 2021-02
dc.identifier.uri https://pubs.acs.org/doi/full/10.1021/acs.orglett.3c00240
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15507
dc.description.abstract A copper(II)-catalyzed cascade synthesis of 1H-pyrrolo[3,4-b]quinoline-1,3(2H)-diones has been achieved from readily available o-amino carbonyl compounds and maleimides. This one-pot cascade strategy involves a copper-catalyzed aza-Michael addition followed by condensation and oxidation to deliver the target molecules. The protocol features a broad substrate scope and excellent functional group tolerance and affords products in moderate to good (44–88%) yields. en_US
dc.language.iso en en_US
dc.publisher ACS en_US
dc.subject Chemistry en_US
dc.subject Quinoline en_US
dc.subject Synthesis en_US
dc.title Copper(II)-Catalyzed Synthesis of Pyrrolo[3,4-b]quinolinediones from o-Amino Carbonyl Compounds and Maleimides en_US
dc.type Article en_US


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