Chiral diamides as efficient catalytic precursors for the borane-mediated asymmetric reduction of prochiral ketones

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Venkateswara Rao, Kalapala
dc.contributor.author Sekhara Reddy, Bhavanam
dc.date.accessioned 2022-03-27T09:01:58Z
dc.date.available 2022-03-27T09:01:58Z
dc.date.issued 2007-05-16
dc.description.abstract Chiral diamides [(2S)-5-oxo-2-(arylamino)carbonylpyrrolidines] derived from the abundantly available (S)-glutamic/(S)-pyroglutamic acids were successfully utilized as effective chiral catalytic precursors in the borane-mediated asymmetric reduction of prochiral ketones in refluxing toluene, to provide the corresponding secondary alcohols with up to 91% enantiomeric purities. © 2007 Elsevier Ltd. All rights reserved.
dc.identifier.citation Tetrahedron Asymmetry. v.18(8)
dc.identifier.issn 09574166
dc.identifier.uri 10.1016/j.tetasy.2007.03.034
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0957416607002935
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12300
dc.title Chiral diamides as efficient catalytic precursors for the borane-mediated asymmetric reduction of prochiral ketones
dc.type Journal. Article
dspace.entity.type
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