Nonsilyl bicyclic secondary amine catalysts for the asymmetric transfer hydrogenation of α, β-unsaturated aldehydes

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dc.contributor.author Kumar, Rohtash
dc.contributor.author Maurya, Vidyasagar
dc.contributor.author Avinash, Avinash
dc.contributor.author Appayee, Chandrakumar
dc.coverage.spatial United States of America
dc.date.accessioned 2024-06-18T15:39:38Z
dc.date.available 2024-06-18T15:39:38Z
dc.date.issued 2024-06
dc.identifier.citation Kumar, Rohtash; Maurya, Vidyasagar; Avinash, Avinash and Appayee, Chandrakumar, "Nonsilyl bicyclic secondary amine catalysts for the asymmetric transfer hydrogenation of α, β-unsaturated aldehydes", The Journal of Organic Chemistry, DOI: 10.1021/acs.joc.4c00523, vol. 89, no. 12, pp. 8586-8600, Jun. 2024.
dc.identifier.issn 0022-3263
dc.identifier.issn 1520-6904
dc.identifier.uri https://doi.org/10.1021/acs.joc.4c00523
dc.identifier.uri https://repository.iitgn.ac.in/handle/123456789/10129
dc.description.abstract The first chiral synthesis of nonsilyl bicyclic secondary amine organocatalysts and their application to the asymmetric transfer hydrogenation of α, β-unsaturated aldehydes are disclosed. A lower catalytic loading (5 mol %) is demonstrated for the reduction of a wide range of α,β-unsaturated aldehydes (up to 97% yield and up to 99% ee). The application of this scalable methodology is showcased for the asymmetric synthesis of bioactive molecules such as phenoxanol, citronellol, ramelteon, and terikalant.
dc.description.statementofresponsibility by Rohtash Kumar, Vidyasagar Maurya, Avinash Avinash and Chandrakumar Appayee
dc.format.extent vol. 89, no. 12, pp. 8586-8600
dc.language.iso en_US
dc.publisher American Chemical Society
dc.title Nonsilyl bicyclic secondary amine catalysts for the asymmetric transfer hydrogenation of α, β-unsaturated aldehydes
dc.type Article
dc.relation.journal The Journal of Organic Chemistry


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