Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/65398
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dc.contributor.authorL Nakkalwar, Shrinivas-
dc.contributor.authorM Kasralikar, Hanmant-
dc.date.accessioned2025-02-20T06:26:33Z-
dc.date.available2025-02-20T06:26:33Z-
dc.date.issued2025-02-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/65398-
dc.description183-191en_US
dc.description.abstractMulticomponent phosphonylation is accomplished by convenient and efficient synthetic method using novel (S)-N- ((cyclohexylmethyl) carbamothioyl) pyrrolidine-2-carboxamide (NCCPC) as bifunctional cyclohexane derived thiourea organocatalyst upon the reaction of an amine, substituted aldehyde with diethyl phosphite. This method not only provides novel and excellent complement for the synthesis but also gives green and transition-metal-free protocol, shows a broad substrate scope, providing a variety of α-amino phosphonates in moderate to good yields.en_US
dc.language.isoenen_US
dc.publisherNIScPR - CSIRen_US
dc.sourceIJC Vol.64(02) [Feb 2025]en_US
dc.subjectMulticomponent phosphorylationen_US
dc.subjectThiourea organocatalysten_US
dc.subjectNCCPCen_US
dc.subjectα-amino phosphonatesen_US
dc.titleSynthesis of α-amino phosphonates catalyzed by bifunctional cyclohexane derived thiourea organocatalysten_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v64i2.15274en_US
Appears in Collections:IJC Vol.64(02) [Feb 2025]

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