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Issue 21, 2007
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Enantioselectivity in the boron aldol reactions of methyl ketones

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Abstract

DFT computed transition states quantitatively explain the surprising stereochemical outcome of unsubstituted enolborinates in diastereoselective and enantioselective boron aldol reactions.

Graphical abstract: Enantioselectivity in the boron aldol reactions of methyl ketones

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Publication details

The article was received on 29 Mar 2007, accepted on 20 Apr 2007 and first published on 01 May 2007


Article type: Communication
DOI: 10.1039/B704786J
Citation: Chem. Commun., 2007, 2124-2126
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    Enantioselectivity in the boron aldol reactions of methyl ketones

    J. M. Goodman and R. S. Paton, Chem. Commun., 2007, 2124
    DOI: 10.1039/B704786J

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