Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/30536
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dc.contributor.authorPatil, Nilesh S-
dc.contributor.authorDeshmukh, Ganesh B-
dc.contributor.authorMahale, Keshao A-
dc.contributor.authorGosavi, Kirankumar S-
dc.contributor.authorPatil, Sambhaji V-
dc.date.accessioned2015-02-12T09:10:26Z-
dc.date.available2015-02-12T09:10:26Z-
dc.date.issued2015-02-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/30536-
dc.description272-278en_US
dc.description.abstractThe syntheses of several novel 3-dialkylamino-N-aryl-maleimides 3a-i and 6 are described via a conjugate elimination-addition-elimination pathway. Syntheses of their various 4-substituted derivatives 4a-i, 5a-c and 7-12 are also described. Introduction of a secondary amino group at C-3 position in N-arylmaleimides leads to the formation of enaminones 3a-i and 6, which undergo facile electrophilic substitutions at C-4 position in good to excellent yields to provide the highly functionalized maleimides 4a-i, 5a-c and 7-12. en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.54B(02) [February 2015]en_US
dc.subjectMaleimideen_US
dc.subjectBrominationen_US
dc.subjectAcylationen_US
dc.subjectVilsmeier-Haack reactionen_US
dc.subjectEnaminoneen_US
dc.titleSynthesis of novel N-aryl-3-dialkylamino-4-substituted maleimidesen_US
dc.typeArticleen_US
Appears in Collections: IJC-B Vol.54B(02) [February 2015]

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