Asymmetric synthesis of α-Arylcyclohexenones catalyzed by Diphenylprolinol Silyl Ether

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dc.contributor.author Mehta, Ronak
dc.contributor.author Kumar, Rohtash
dc.contributor.author Singh, Suraj
dc.contributor.author Appayee, Chandrakumar
dc.coverage.spatial United States of America
dc.date.accessioned 2024-08-02T14:02:37Z
dc.date.available 2024-08-02T14:02:37Z
dc.date.issued 2024-08
dc.identifier.citation Mehta, Ronak; Kumar, Rohtash; Singh, Suraj and Appayee, Chandrakumar, "Asymmetric synthesis of α-Arylcyclohexenones catalyzed by Diphenylprolinol Silyl Ether", The Journal of Organic Chemistry, DOI: 10.1021/acs.joc.4c01234, vol. 89, no. 15, pp. 10892-10902, Aug. 2024.
dc.identifier.issn 0022-3263
dc.identifier.issn 1520-6904
dc.identifier.uri https://doi.org/10.1021/acs.joc.4c01234
dc.identifier.uri https://repository.iitgn.ac.in/handle/123456789/10283
dc.description.abstract A general methodology for the asymmetric synthesis of α-arylcyclohexeneones from arylacetones and α,β-unsaturated aldehydes catalyzed by diphenylprolinol silyl ether followed by p-TSA-mediated cyclization is developed. A variety of arylacetones and α,β-unsaturated aldehydes were successfully converted to α-arylcyclohexeneones in 34–67% yield, 10:1–100:0 dr, and 81–99% ee. The scalability of this methodology by a gram-scale synthesis and their utility by converting the product to the corresponding epoxide, alcohol, and diol are demonstrated.
dc.description.statementofresponsibility by Ronak Mehta, Rohtash Kumar, Suraj Singh and Chandrakumar Appayee
dc.format.extent vol. 89, no. 15, pp. 10892-10902
dc.language.iso en_US
dc.publisher American Chemical Society
dc.title Asymmetric synthesis of α-Arylcyclohexenones catalyzed by Diphenylprolinol Silyl Ether
dc.type Article
dc.relation.journal The Journal of Organic Chemistry


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