A highly efficient and green cascade synthesis of 3-methyl-substituted-4- hydroxy-1-methyl-quinolin-2(1H)-ones under solvent- and catalyst-free conditions

Please use this identifier to cite or link to this item: https://idr.nitk.ac.in/jspui/handle/123456789/9610

Full metadata record

DC Field	Value	Language
dc.contributor.author	Bhat, S.I.
dc.contributor.author	Trivedi, D.R.
dc.date.accessioned	2020-03-31T06:51:12Z	-
dc.date.available	2020-03-31T06:51:12Z	-
dc.date.issued	2014
dc.identifier.citation	RSC Advances, 2014, Vol.4, 22, pp.11300-11304	en_US
dc.identifier.uri	10.1039/c3ra45208e
dc.identifier.uri	http://idr.nitk.ac.in/jspui/handle/123456789/9610	-
dc.description.abstract	An expeditious and green protocol for the synthesis of 3,3?- methanediylbis(4-hydroxy-1-methylquinolin-2(1H)-one) (MDBHQ) derivatives and 3-((2-amino-6-oxocyclohex-1-enyl)methyl)-4-hydroxy-1-methylquinolin-2(1H)-one (AOCHQ) derivatives has been developed via a cascade Knoevenagel-Michael reaction. The products were obtained in high yield under neat reaction conditions without any work-up or chromatographic purification. The generality and functional tolerance of this environmentally benign protocol is demonstrated. 2014 The Royal Society of Chemistry.	en_US
dc.title	A highly efficient and green cascade synthesis of 3-methyl-substituted-4- hydroxy-1-methyl-quinolin-2(1H)-ones under solvent- and catalyst-free conditions	en_US
dc.type	Article	en_US
Appears in Collections:	1. Journal Articles

Files in This Item:

There are no files associated with this item.