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

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DC Field	Value	Language
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
Appears in Collections:	Department of Chemistry

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