(2S)-2-Anilinomethylpyrrolidine: an efficient in situ recyclable chiral catalytic source for the borane-mediated asymmetric reduction of prochiral ketones in refluxing toluene
(2S)-2-Anilinomethylpyrrolidine: an efficient in situ recyclable chiral catalytic source for the borane-mediated asymmetric reduction of prochiral ketones in refluxing toluene
| dc.contributor.author | Basavaiah, Deevi | |
| dc.contributor.author | Rao, Kalapala Venkateswara | |
| dc.contributor.author | Reddy, Bhavanam Sekhara | |
| dc.date.accessioned | 2022-03-27T09:02:13Z | |
| dc.date.available | 2022-03-27T09:02:13Z | |
| dc.date.issued | 2006-04-03 | |
| dc.description.abstract | (2S)-2-Anilinomethylpyrrolidine was successfully utilized as a chiral catalytic source in the borane-mediated asymmetric reduction of prochiral ketones in refluxing toluene to provide the corresponding secondary alcohols with enantiomeric excesses up to 91%. The potential of (2S)-2-anilinomethylpyrrolidine as an in situ recyclable chiral catalytic source in the borane-mediated chiral reduction processes has also been demonstrated. © 2006 Elsevier Ltd. All rights reserved. | |
| dc.identifier.citation | Tetrahedron Asymmetry. v.17(7) | |
| dc.identifier.issn | 09574166 | |
| dc.identifier.uri | 10.1016/j.tetasy.2006.03.021 | |
| dc.identifier.uri | https://www.sciencedirect.com/science/article/abs/pii/S095741660600200X | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/12307 | |
| dc.title | (2S)-2-Anilinomethylpyrrolidine: an efficient in situ recyclable chiral catalytic source for the borane-mediated asymmetric reduction of prochiral ketones in refluxing toluene | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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