Discovery of C3H8O2

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Application 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 Application of 4254-15-3

Application of 4254-15-3, Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction by binding to a specific portion of an enzyme and thus slowing or preventing a reaction from occurring. In a document type is Article, and a compound is mentioned, 4254-15-3, Name is (S)-Propane-1,2-diol, introducing its new discovery.

Stereo selective formation of cyclic carbamates was achieved by the intramolecular trapping of a tert-butyldimethylsilyloxycarbonyl group with allylic esters upon activation with fluoride and cat. Pd(O). The reactive conformation is proposed to be D. The highly stereo;elective reaction of 2 allylic esters allowed a detailed reaction mechanism to be proposed which accounts for the observed selectivities.

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Application 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 Application 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