Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/59817
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dc.contributor.authorGanesh, N S-
dc.contributor.authorSpandana, K V L D-
dc.contributor.authorNarsaiah, A Venkat-
dc.date.accessioned2022-05-31T06:56:39Z-
dc.date.available2022-05-31T06:56:39Z-
dc.date.issued2022-05-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/59817-
dc.description503-507en_US
dc.description.abstractA simple and efficient route has been developed for enantioselective synthesis of hyperparathyroidism agent (R)-Cinacalcet. The synthesis started from commercially available triflouromethyl benzaldehyde and 1-(naphthalen-1-yl) ethanone and completed in 8 steps with an overall yield 18.5%. The key reactions involved are Corey-Bakshi-Shibata chiral reduction and reductive amination.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.61(05) [May 2022]en_US
dc.subjectWittig reactionen_US
dc.subjectCBS-reductionen_US
dc.subjectoxidationen_US
dc.subjectreductive aminationen_US
dc.subjecthyperparathyroidismen_US
dc.titleEnantioselective synthesis of hyperparathyroidism agent Cinacalcet hydrochlorideen_US
dc.typeArticleen_US
Appears in Collections:IJC Vol.61(05) [May 2022]

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