1356827-93-4Relevant articles and documents
Exploring the potential of some yeast strains in the stereoselective synthesis of aldol reaction products and its reduced 1,3-dialcohol derivatives
Andreu, Cecilia,Del Olmo, Marcelli
, p. 57 - 61 (2013/06/27)
The behavior of two yeast strains has been studied under different conditions. Both microorganims catalyzed the aldol reaction between activated aldehydes and acetone when a large amount of the latter was present in the reaction medium producing, with mod
One-pot chemoenzymatic synthesis of chiral 1,3-diols using an enantioselective aldol reaction with chiral Zn2+ complex catalysts and enzymatic reduction using oxidoreductases with cofactor regeneration
Sonoike, Shotaro,Itakura, Toshinari,Kitamura, Masanori,Aoki, Shin
experimental part, p. 64 - 74 (2012/04/04)
We previously reported on enantioselective aldol reactions of acetone and some aldehydes catalyzed by chiral Zn2+ complexes of L-prolyl-pendant [12]aneN4 (L-ZnL1) and L-valyl-pendant [12]aneN 4 (L-ZnL2/sup