Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/60829
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dc.contributor.authorShit, Prasenjit-
dc.contributor.authorSingha, Raju-
dc.date.accessioned2022-11-11T10:21:55Z-
dc.date.available2022-11-11T10:21:55Z-
dc.date.issued2022-11-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/60829-
dc.description1159-1163en_US
dc.description.abstractA one-pot two-step methodology has been developed for the synthesis of 4,5-dibromo-3,6-diarylpyridazines starting from easily available starting material 1,4-diarylbuta-1,3-diynes. The reaction goes through the electrophilic addition of Br+ ion with alkyne bonds followed by nucleophilic addition of hydrazine and intramolecular cyclization.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.61(11) [Nov 2022]en_US
dc.subjectDiyneen_US
dc.subjectNBSen_US
dc.subjectCyclizationen_US
dc.subjectOne pot reactionen_US
dc.subjectPyridazineen_US
dc.titleOne pot synthesis of 4,5-dibromo-3,6-diarylpyridazine from 1,4-diarylbuta- 1,3-diyneen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v61i11.63897en_US
Appears in Collections:IJC Vol.61(11) [Nov 2022]

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