Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/62518
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dc.contributor.authorAnnapurna, K-
dc.contributor.authorZeenath, S Fatima-
dc.contributor.authorNarsaiah, A Venkat-
dc.date.accessioned2023-09-19T05:16:52Z-
dc.date.available2023-09-19T05:16:52Z-
dc.date.issued2023-09-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/62518-
dc.description940-944en_US
dc.description.abstractA simple synthesis of a novel fungicide mandipropamid has been achieved in six steps, with an overall yield of 43%. Synthesis has been carried out from commercially available starting materials, 4-chloroacetophenone and vanillin. The key steps involved in the synthesis are Cannizzaro and Henry reactions, amide bond formation and O-propargylation.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR,Indiaen_US
dc.sourceIJC Vol.62(09) [September 2023]en_US
dc.subjectMandipropamiden_US
dc.subjectFungicideen_US
dc.subjectCannizzaro reactionen_US
dc.subjectHenry reactionen_US
dc.subjectAmideen_US
dc.titleSynthesis of crop protection agent mandipropamiden_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v62i9.3120en_US
Appears in Collections:IJC Vol.62(09) [September 2023]

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