Reference of 850222-40-1, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C–H bond functionalisation has revolutionised modern synthetic chemistry. 850222-40-1, Name is (S)-3-(Dimethylamino)-1-(3-methoxyphenyl)-2-methylpropan-1-one, SMILES is O=C(C1=CC=CC(OC)=C1)[C@@H](C)CN(C)C, belongs to chiral-catalyst compound. In a article, author is Yin, Yanli, introduce new discover of the category.
A radical-based asymmetric olefin difunctionalization strategy for rapidly forging all-carbon quaternary stereocenters alpha to diverse azaarenes is reported. Under cooperative photoredox and chiral Bronsted acid catalysis, cyclopropylamines with alpha-branched 2-vinylazaarenes can undergo a sequential two-step radical process, furnishing various valuable chiral azaarene-substituted cyclopentanes. The use of the rigid and confined C-2-symmetric imidodiphosphoric acid catalysts achieves high enantio- and diastereo-selectivities for these asymmetric [3 + 2] cycloadditions.
Reference of 850222-40-1, 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 850222-40-1 is helpful to your research.
Reference:
Chiral Catalysts,
,Chiral catalysts – SlideShare