Recently I am researching about ENANTIOSELECTIVE SYNTHESIS; TRANSFER HYDROGENATION; ALIPHATIC-KETONES; SILICON-COMPOUNDS; PENTACOORDINATE; REAGENTS; PHOSPHORUS; REACTIVITY; COMPLEXES, Saw an article supported by the Northern Illinois University; Ryerson University. Name: 1-(4-Nitrophenyl)ethanone. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Skrypai, V; Varjosaari, SE; Azam, F; Gilbert, TM; Adler, MJ. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone
The asymmetric direct reductive amination of prochiral ketones with aryl amines using 1-hydrosilatrane with a chiral Bronsted acid catalyst is reported. This is the first known example of chiral Bronsted acid-catalyzed asymmetric reductive amination using a silane as the hydride source. The reaction features a highly practical reducing reagent and proceeds efficiently at room temperature without a specialized reaction setup or equipment to exclude air or moisture. This method provides high conversion and enantiomeric excess up to 84% of the desired chiral secondary amines with minimal side products.
Welcome to talk about 100-19-6, If you have any questions, you can contact Skrypai, V; Varjosaari, SE; Azam, F; Gilbert, TM; Adler, MJ or send Email.. Name: 1-(4-Nitrophenyl)ethanone
Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem