Extended knowledge of (1R,2S)-(−)-2-Amino-1,2-diphenylethanol

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application In Synthesis of (1R,2S)-(−)-2-Amino-1,2-diphenylethanol. In my other articles, you can also check out more blogs about 23190-16-1

23190-16-1, Name is (1R,2S)-(−)-2-Amino-1,2-diphenylethanol, molecular formula is C6H5CH(NH2)CH(C6H5)OH, belongs to chiral-catalyst compound, is a common compound. In a patnet, once mentioned the new application about 23190-16-1, Application In Synthesis of (1R,2S)-(−)-2-Amino-1,2-diphenylethanol

Enantioselectivity in the allylboration of W-silylimines with a variety of chirally modified allylboron reagents has been examined. Optically active N-sulfonylarhino alcohols (16,17 and 19) derived from D-camphor and norephedrine were found to be efficient chiral ligands for the allylboration reagent. These reagents smoothly reacted with Ar-silylimines to give the corresponding homoallylic amines in a high level of enantioselectivity up to 96% ee.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application In Synthesis of (1R,2S)-(−)-2-Amino-1,2-diphenylethanol. In my other articles, you can also check out more blogs about 23190-16-1

Reference:
Chiral Catalysts,
Chiral catalysts – SlideShare