1204698-90-7

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 117184-95-9 4-(4-chlorophenyl)-4-hydroxybutan-2-one 
• 30626-03-0 (3E)-4-(4-chlorophenyl)-3-buten-2-one 

Relevant academic research and scientific papers

Exploring the potential of some yeast strains in the stereoselective synthesis of aldol reaction products and its reduced 1,3-dialcohol derivatives

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

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

Catalytic 1,3-difunctionalisation of organic backbones through a highly stereoselective, one-pot, boron conjugate-addition/reduction/oxidation process

A simple one-pot, three-step synthetic route to chiral 1,3-amino alcohols and 1,3-diols has been established. Considering the overall stereocontrol of the synthetic protocol, the first and key step is an enantioselective β-boration of α,β-unsaturated imin

Sequential and modular synthesis of chiral 1,3-diols with two stereogenic centers: Access to all four stereoisomers by combination of organo- and biocatalysis

Chemical Equitation Presentation Biocompatible: A modular chemoenzymatic synthesis (see scheme) based on asymmetric organo- and biocatalytic reaction sequences allows the sequential construction of both stereogenic centers of 1,3-diols and leads to all fo