Issue 38, 2007

Direct asymmetric catalytic 1,2-addition of RZnX to aldehydes promoted by AlMe3 and reversal of expected stereochemistry

Abstract

Addition of AlMe3 to commercial THF solutions of RZnX (R = aryl, functionalised aryl, vinyl; X = Br, I) simultaneously promotes Schlenk equilibria (leading to competent nucleophiles) and the formation of an Al–Zn-ligand catalyst delivering 80–90% ee for Ar1CH(OH)Ar2 formation from aldehydes.

Graphical abstract: Direct asymmetric catalytic 1,2-addition of RZnX to aldehydes promoted by AlMe3 and reversal of expected stereochemistry

Supplementary files

Article information

Article type
Communication
Submitted
12 Jul 2007
Accepted
26 Jul 2007
First published
15 Aug 2007

Chem. Commun., 2007, 3945-3947

Direct asymmetric catalytic 1,2-addition of RZnX to aldehydes promoted by AlMe3 and reversal of expected stereochemistry

J. Shannon, D. Bernier, D. Rawson and S. Woodward, Chem. Commun., 2007, 3945 DOI: 10.1039/B710681E

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