A new chiral catalytic source with an N-P=O structural framework containing a proximal hydroxyl group for the borane-mediated asymmetric reduction of prochiral ketones
A new chiral catalytic source with an N-P=O structural framework containing a proximal hydroxyl group for the borane-mediated asymmetric reduction of prochiral ketones
| dc.contributor.author | Basavaiah, Deevi | |
| dc.contributor.author | Reddy, Gone Jayapal | |
| dc.contributor.author | Chandrashekar, Vanampally | |
| dc.date.accessioned | 2022-03-27T09:02:31Z | |
| dc.date.available | 2022-03-27T09:02:31Z | |
| dc.date.issued | 2004-01-12 | |
| dc.description.abstract | (5S)-2-[(1R,2R,3S,5R)-2-Hydroxy-2,6,6-trimethylbicyclo[3.1.1] heptan-3-yloxy]-1,3-diaza-2-phospha-2-oxo-3-phenylbicyclo[3.3.0]octane has been successfully employed as a novel chiral catalytic source (4mol%) for borane-mediated asymmetric reduction of prochiral ketones thus providing the resulting secondary alcohols with up to 96% enantiomeric excess. © 2003 Elsevier Ltd. All rights reserved. | |
| dc.identifier.citation | Tetrahedron Asymmetry. v.15(1) | |
| dc.identifier.issn | 09574166 | |
| dc.identifier.uri | 10.1016/j.tetasy.2003.11.002 | |
| dc.identifier.uri | https://www.sciencedirect.com/science/article/abs/pii/S0957416603009066 | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/12316 | |
| dc.title | A new chiral catalytic source with an N-P=O structural framework containing a proximal hydroxyl group for the borane-mediated asymmetric reduction of prochiral ketones | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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