Synthesis of chiral α-diarylacetic esters by stereospecific 1,2-aryl migration promoted by in situ generated acetals from benzoins
Synthesis of chiral α-diarylacetic esters by stereospecific 1,2-aryl migration promoted by in situ generated acetals from benzoins
| dc.contributor.author | Kothapalli, Raveendra Babu | |
| dc.contributor.author | Niddana, Ramana | |
| dc.contributor.author | Balamurugan, Rengarajan | |
| dc.date.accessioned | 2022-03-27T08:39:25Z | |
| dc.date.available | 2022-03-27T08:39:25Z | |
| dc.date.issued | 2014-03-07 | |
| dc.description.abstract | A simple protocol for the synthesis of α-diarylacetic esters from benzoins is described. In situ generated acetal assists rapid 1,2-aryl migration in a stereospecific manner, paving the way to make enantioenriched α-diarylacetic esters from easily accessible enantiopure benzoins. © 2014 American Chemical Society. | |
| dc.identifier.citation | Organic Letters. v.16(5) | |
| dc.identifier.issn | 15237060 | |
| dc.identifier.uri | 10.1021/ol500292c | |
| dc.identifier.uri | https://pubs.acs.org/doi/10.1021/ol500292c | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/11386 | |
| dc.title | Synthesis of chiral α-diarylacetic esters by stereospecific 1,2-aryl migration promoted by in situ generated acetals from benzoins | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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