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 |
|