Ruthenium-catalyzed cyclization of N-carbamoyl indolines with alkynes: an efficient route to pyrroloquinolinones

dc.contributor.author	Manoharan, Ramasamy	en_US
dc.contributor.author	JEGANMOHAN, MASILAMANI	en_US
dc.date.accessioned	2019-03-15T11:24:16Z
dc.date.available	2019-03-15T11:24:16Z
dc.date.issued	2015-07	en_US
dc.identifier.citation	Organic and Biomolecular Chemistry, 13(35), 9276-9284.	en_US
dc.identifier.issn	9276-9284	en_US
dc.identifier.issn	1477-0539	en_US
dc.identifier.uri	http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2212
dc.identifier.uri	https://doi.org/10.1039/C5OB01146A	en_US
dc.description.abstract	A regioselective synthesis of substituted pyrroloquinolinones via a ruthenium-catalyzed oxidative cyclization of substituted N-carbamoyl indolines with alkynes is described. The cyclization reaction was compatible with various symmetrical and unsymmetrical alkynes including substituted propiolates. Later, we performed the aromatization of pyrroloquinolinones into indole derivatives in the presence of 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ).	en_US
dc.language.iso	en	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	Catalyzed cyclization	en_US
dc.subject	Pyrroloquinolinones	en_US
dc.subject	Transition metal-catalyzed	en_US
dc.subject	Cyclization reaction	en_US
dc.subject	2015	en_US
dc.title	Ruthenium-catalyzed cyclization of N-carbamoyl indolines with alkynes: an efficient route to pyrroloquinolinones	en_US
dc.type	Article	en_US
dc.contributor.department	Dept. of Chemistry	en_US
dc.identifier.sourcetitle	Organic and Biomolecular Chemistry	en_US
dc.publication.originofpublisher	Foreign	en_US