Crystallization assisted dynamic kinetic resolution for the synthesis of (R)-ß-methylphenethylamine.

This study explores a combination of the concept of enantioselective enzymatic synthesis of ß-chiral amines through transamination with in situ product crystallization (ISPC) to overcome product inhibition. Using 2-phenylpropanal as a readily available and easily racemizing substrate of choice, (R)-ß-methylphenethylamine ((R)-2-phenylpropan-1-amine) concentrations of up to 250 mM and enantiomeric excesses of up to 99 % are achieved when using a commercially available transaminase from Ruegeria pomeroyi in a fed-batch based dynamic kinetic resolution reaction on preparative scale. The source of substrate decomposition during the reaction is also investigated and the resulting unwanted byproduct formation is successfully reduced to insignificant levels.

Merging High-Pressure Syngas Metal Catalysis and Biocatalysis in Tandem One-Pot Processes for the Synthesis of Non-chiral and Chiral Alcohols from Alkenes in Water.

While simultaneously proceeding reactions are among the most fascinating features of biosynthesis, this concept of tandem processes also offers high potential in the chemical industry in terms of less waste production and improved process efficiency and sustainability. Although examples of one-pot chemoenzymatic syntheses exist, the combination of completely different reaction types is rare. In this work, we demonstrate that extreme "antipodes" of the "worlds of catalysis" such as syngas-based high-pressure hydroformylation and biocatalyzed reduction can be combined within a tandem­type one-pot process in water, which both play an outstanding role as individual reactions. No significant deactivation was found for either the biocatalyst or the chemocatalyst. A proof­of­concept for the one-pot process starting from 1-octene was established with >99% conversion and 80% isolated yield of the desired alcohol isomers. All necessary components for hydroformylation and biocatalysis were added to the reactor from the beginning. This concept has been extended to chiral products by conducting the hydroformylation of styrene and an enzymatic dynamic kinetic resolution in a tandem mode, leading to an excellent conversion of >99% and an enantiomeric ratio of 91:9 to (S)­2-phenylpropanol. The overall process runs in water under mild and energy-saving conditions, without any need for intermediate isolation.