PEG-400 mediated and promoted eco-friendly one-pot synthesis of isoxazolyl pyridines, quinolines and 3-hydroxy-2-oxoindoles through <em>sp</em><sup>3</sup> C-H bond functionalization of methyl aza-arenes

Nagaraju, D; Kishore, B; Thirupathaiah, K; Rajanarendar, E

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Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/43083

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DC Field	Value	Language
dc.contributor.author	Nagaraju, D	-
dc.contributor.author	Kishore, B	-
dc.contributor.author	Thirupathaiah, K	-
dc.contributor.author	Rajanarendar, E	-
dc.date.accessioned	2017-11-13T09:11:49Z	-
dc.date.available	2017-11-13T09:11:49Z	-
dc.date.issued	2017-11	-
dc.identifier.issn	0975-0983(Online); 0376-4699(Print)	-
dc.identifier.uri	http://nopr.niscair.res.in/handle/123456789/43083	-
dc.description	1193-1199	en_US
dc.description.abstract	Polyethylene glycol (PEG) promoted functionalization of sp³ C-H bonds of methyl aza -arenes with 3-methyl-4-nitro-5-styrylisoxazoles for construction of isoxazolyl pyridines 3 and quinolines 5 is described. Nitrostyrylisoxazoles are proved to be good C=C elctrophilic acceptors for the construction of various azaarene-containing Michael addition products. Functionalization of sp³ C-H bonds of 3,5-dimethyl-4-nitroisoxazole is also described for synthesis of biologically active isoxazolyl 3-hydroxy-2-oxoindoles 8.	en_US
dc.language.iso	en_US	en_US
dc.publisher	NISCAIR-CSIR, India	en_US
dc.rights	CC Attribution-Noncommercial-No Derivative Works 2.5 India	en_US
dc.source	IJC-B Vol.56B(11) [November 2017]	en_US
dc.subject	C-H activation	en_US
dc.subject	Michael addition	en_US
dc.subject	Isoxazole	en_US
dc.subject	Azaarene	en_US
dc.subject	Isatin	en_US
dc.title	PEG-400 mediated and promoted eco-friendly one-pot synthesis of isoxazolyl pyridines, quinolines and 3-hydroxy-2-oxoindoles through sp³ C-H bond functionalization of methyl aza-arenes	en_US
dc.type	Article	en_US
Appears in Collections:	IJC-B Vol.56B(11) [November 2017]

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