Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/28935
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dc.contributor.authorChand, Subhash-
dc.contributor.authorSuresh-
dc.contributor.authorSandhu, Jagir S-
dc.date.accessioned2014-06-12T05:03:37Z-
dc.date.available2014-06-12T05:03:37Z-
dc.date.issued2014-06-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/28935-
dc.description728-732en_US
dc.description.abstract1,3-Dimethyl-2,4,7-trioxo-5-aryl-1,2,3,4,7,8-hexahydropyrido[2,3-d]pyrimidine-6-carbonitriles have been synthesized via tandem Michael-Cyclization of 6-aminouracils with arylidene ethylcyanoacetates employing catalytic amount of BiCl3. Under mild reaction conditions, pyrido[2,3-d]pyrimidines have been obtained in very good yields in one pot.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.53B(06) [June 2014]en_US
dc.subjectPyrido[2,3-d]pyrimidinesen_US
dc.subjectTandem-Michael-cyclizationen_US
dc.subjectBiCl3en_US
dc.subject6-aminouracilsen_US
dc.subjectArylidene ethylcyanoacetateen_US
dc.titlePyrido[2,3-d]pyrimidines: A novel tandem Michael cyclization of 6-aminouracils with arylidenecyanoacetate using BiCl3en_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.53B(06) [June 2014]

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