You Should Know Something about 4254-15-3

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Electric Literature of 4254-15-3, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about Electric Literature of 4254-15-3

Electric Literature of 4254-15-3, New Advances in Chemical Research in 2021. Irreversible inhibitors are therefore the equivalent of poisons in heterogeneous catalysis. 4254-15-3, Name is (S)-Propane-1,2-diol, molecular formula is C3H8O2, belongs to chiral-oxygen-ligands compounds. In a Article，once mentioned of 4254-15-3

A series of -amino alcohols derivatives were synthesized from (R)-2-amino-1-butanol and (S)-1,2-propanediol, and they have been used as organocatalaysts in the racemic ring opening of epoxide in good yields with high enantiomeric excess (up to 97%). Copyright

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Electric Literature of 4254-15-3, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about Electric Literature of 4254-15-3

Reference：
Synthesis and Crystal Structure of a Chiral C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur–nitrogen–oxygen ligand derived from aminothiourea and sodium D-camphor-β-sulfonate