Alberg David G, Poulsen Thomas B, Bertelsen Søren, Christensen Kasper L, Birkler Rune D, Johannsen Mogens, Jørgensen Karl Anker
Center for Catalysis, Department of Chemistry, Aarhus University, Aarhus C, Denmark.
Bioorg Med Chem Lett. 2009 Jul 15;19(14):3888-91. doi: 10.1016/j.bmcl.2009.03.128. Epub 2009 Mar 28.
The aldol reaction of the endogeneous compounds acetone and methylglyoxal has been studied using organocatalysis in relation to biologically relevant non-enzymatic reactions. Under preparative conditions, 3-hydroxy-2,5-hexadione, known as Henze's ketol, is formed in high yield and with enantioselectivities up to 88% ee. Furthermore, Henze's ketol is also formed under simulated physiological conditions at micromolar scale, indicating that this reaction might take place in living organisms.