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dc.contributor.authorNagaraju, D-
dc.contributor.authorKishore, B-
dc.contributor.authorThirupathaiah, K-
dc.contributor.authorRajanarendar, E-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.description.abstractPolyethylene 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.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.56B(11) [November 2017]en_US
dc.subjectC-H activationen_US
dc.subjectMichael additionen_US
dc.titlePEG-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-arenesen_US
Appears in Collections:IJC-B Vol.56B(11) [November 2017]

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