Sunden, Henrik; Rios, Ramon; Ibrahem, Ismail; Zhao, Gui-Ling; Eriksson, Lars; Cordova, Armando published the artcile< A highly enantioselective catalytic domino aza-Michael/aldol reaction: one-pot organocatalytic asymmetric synthesis of 1,2-dihydroquinolines>, Application of C9H7BrO, the main research area is stereoselective Michael aldol aminobenzaldehyde unsaturated aldehyde catalyst.
The highly enantioselective organocatalytic domino aza-Michael/aldol reaction is presented. The unprecedented, chiral amine-catalyzed asym. domino reactions between 2-aminobenzaldehydes and α,β-unsaturated aldehydes proceed with excellent chemo- and enantioselectivity to give the corresponding pharmaceutically valuable 1,2-dihydroquinolines in high yields with 90 to > 99 % ee.
Advanced Synthesis & Catalysis published new progress about Aldol condensation catalysts, stereoselective. 3893-18-3 belongs to class bromides-buliding-blocks, and the molecular formula is C9H7BrO, Application of C9H7BrO.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary