1289423-47-7Relevant articles and documents
The construction of quaternary stereocenters by the Henry reaction: Circumventing the usual reactivity of substituted glyoxals
Blay, Gonzalo,Hernandez-Olmos, Victor,Pedro, Jose R.
supporting information; experimental part, p. 3768 - 3773 (2011/05/04)
The enantioselective Henry reaction between alkyl- and arylglyoxal hydrates and nitromethane catalyzed by CuII-iminopyridine complexes takes place regioselectively on the ketone carbonyl group to give chiral tertiary nitroaldols with high functional group density and enantiomeric excesses of up to 96 %. Both aromatic and aliphatic glyoxals are suitable substrates for this reaction.