The important role of 3082-64-2

Reference of 3082-64-2, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about 3082-64-2 is helpful to your research.

Reference of 3082-64-2, Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. The appropriate choice of redox mediator can avoid electrode passivation and overpotential. 3082-64-2, Name is (R)-1-Phenylpropan-1-amine, SMILES is N[C@H](CC)C1=CC=CC=C1, belongs to chiral-catalyst compound. In a article, author is Zhu, Wen-Run, introduce new discover of the category.

A catalytic asymmetric oxa-1,3-dipolar cycloaddition of ketones with trifluoroethylamine-derived azomethine ylides has been developed using cinchona-derived bifunctional thiourea catalysts. This protocol provides an efficient methodology for the facile synthesis of chiral CF3-containing oxazolidines with moderate to excellent yields, excellent diastereoselectivities and enantioselectivities (58-98% yields, up to >20 : 1 dr and 98% ee). Remarkably, these oxazolidines could be facilely converted to CF3-containing 1,2-amino alcohols with vicinal stereogenic centers, which is a privileged structural motif in medicinal chemistry.

Reference of 3082-64-2, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about 3082-64-2 is helpful to your research.

Reference:
Chiral Catalysts,
,Chiral catalysts – SlideShare