Li, Chenghao published the artcileRuthenium-catalyzed enantioselective hydrogenation of quinoxalinones and quinazolinones, Application In Synthesis of 1885-29-6, the main research area is quinoxalinone ruthenium catalyst enantioselective hydrogenation; dihydroquinoxalinone preparation; quinazolinone ruthenium catalyst enantioselective hydrogenation; dihydroquinazolinone preparation.
An efficient Ru-catalyzed enantioselective hydrogenation of quinoxalinone and quinazolinone derivatives was successfully developed, provided a straightforward and facile access to chiral dihydroquinoxalinones and dihydroquinazolinones with excellent results (89-98% yields, up to 98% ee). Importantly, the key enantiopure dihydroquinoxalinone intermediate towards the synthesis of a bioactive BRD4 inhibitor was conveniently synthesized by this catalytic hydrogenation methodol.
Organic Chemistry Frontiers published new progress about Aromatic diamines Role: RCT (Reactant), RACT (Reactant or Reagent). 1885-29-6 belongs to class nitriles-buliding-blocks, name is 2-Aminobenzonitrile(Flakes or Chunks), and the molecular formula is C7H6N2, Application In Synthesis of 1885-29-6.
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts