Direct catalytic synthesis of densely substituted 3-formylpyrroles from imines and 1,4-ketoaldehydes

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DC Field	Value	Language
dc.contributor.author	Kumar, Indresh	-
dc.date.accessioned	2021-10-27T04:27:54Z	-
dc.date.available	2021-10-27T04:27:54Z	-
dc.date.issued	2014	-
dc.identifier.uri	https://pubs.rsc.org/en/content/articlelanding/2014/ra/c4ra06581f	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3173	-
dc.description.abstract	A sustainable method for the direct access to highly substituted 3-formylpyrroles from 1,4-ketoaldehydes and imine via formal [3 + 2] cycloaddition is reported. This reaction involves a one-pot amine catalyzed chemoselective Mannich-cyclization-aerobic oxidation sequence with good to high yields. Further application of the gram scale reaction as well as synthesis of fully substituted 3-formylpyrrole is also shown.	en_US
dc.language.iso	en	en_US
dc.publisher	RSC	en_US
dc.subject	Chemistry	en_US
dc.subject	Synthesis	en_US
dc.subject	3-formylpyrroles	en_US
dc.subject	Ketoaldehydes	en_US
dc.title	Direct catalytic synthesis of densely substituted 3-formylpyrroles from imines and 1,4-ketoaldehydes	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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