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 |
|