Towards chiral diamines as chiral catalytic precursors for the borane-mediated enantioselective reduction of prochiral ketones

dc.contributor.author	Basavaiah, Deevi
dc.contributor.author	Das, Utpal
dc.contributor.author	Roy, Suparna
dc.date.accessioned	2022-03-27T09:01:46Z
dc.date.available	2022-03-27T09:01:46Z
dc.date.issued	2009-01-01
dc.description.abstract	Two chiral diamines (3S)-3-anilinomethyl-1,2,3,4-tetrahydroisoquinoline (1) and (2R)-2- anilinomethylpiperidine (2) have been employed as chiral catalytic sources in the borane-mediated asymmetric reduction of prochiral ketones thus providing the resulting secondary alcohols in good enantiomeric purities (up to 81% ee). © Indian Academy of Sciences.
dc.identifier.citation	Journal of Chemical Sciences. v.121(6)
dc.identifier.issn	09743626
dc.identifier.uri	10.1007/s12039-009-0112-x
dc.identifier.uri	http://link.springer.com/10.1007/s12039-009-0112-x
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/12294
dc.subject	(2R)-2- anilinomethylpiperidine
dc.subject	(3S)-3-Anilinomethyl-1,2,3,4-tetrahydroisoquinoline
dc.subject	(S)-phenylalanine
dc.subject	Asymmetric reduction
dc.title	Towards chiral diamines as chiral catalytic precursors for the borane-mediated enantioselective reduction of prochiral ketones
dc.type	Journal. Article
dspace.entity.type

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