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Lookup NU author(s): Dr Simon Jones
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The dependency of the enantioselectivity on the solvent and hydride source for the asymmetric reduction of acetophenone catalysed by the oxazaborolidine derived from cis-(1R,2S)-1-amino-indan-2-ol have been investigated. 11B NMR studies have implied that monomer/dimer ratios are important for achieving high enantioselectivities. © 2003 Elsevier Ltd. All rights reserved.
Author(s): Gilmore NJ, Jones S
Publication type: Article
Publication status: Published
Journal: Tetrahedron: Asymmetry
ISSN (print): 0957-4166
ISSN (electronic): 1362-511X
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