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Please use this identifier to cite or link to this item: http://dspace.library.iitb.ac.in/jspui/handle/10054/12402

Title: Enantioselective Synthesis of Phenyl-ethanolamines Through Application of Chiral Sulfoxide
Authors: SIVAKUMAR, AV
LAHOTI, AM
BHAT, SV
Keywords: asymmetric reduction
amino-acids
hydrogenation
cyanohydrins
derivatives
resolution
chemistry
alcohols
ketones
oxides
Issue Date: 2009
Publisher: TAYLOR & FRANCIS INC
Citation: SYNTHETIC COMMUNICATIONS, 39(18), 3338-3347
Abstract: Efficient enantioselective synthesis of (R)- and (S)-enantiomers of 2-(tert-butylamino)-1-(p-methoxyphenyl)-ethanol has been achieved in high enantiomeric excess by using asymmetric sulfoxide as a chiral auxiliary. The present synthetic approach was further extended to the asymmetric synthesis of (R)-salbutamol.
URI: http://dx.doi.org/10.1080/00397910902765578
http://dspace.library.iitb.ac.in/xmlui/handle/10054/12402
http://hdl.handle.net/10054/12402
ISSN: 0039-7911
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