1255772-62-3Relevant academic research and scientific papers
Assisted tandem palladium(II)/palladium(0)-catalyzed C-and N-Arylations of quinoxalin-2(1H)-ones in water
Carrr, Amandine,Brion, Jean-Daniel,Alami, Mouad,Messaoudi, Samir
supporting information, p. 3821 - 3830 (2015/01/16)
A straightforward assisted tandem palladium(II)-and palladium(0)-catalyzed direct C-3 and N-4 arylation of quinoxalin-2(1H)-ones with boronic acids and aryl halides in water as safe and cheap solvent is reported. This environmentally friendly catalytic protocol is compatible with a wide range of functional groups and allows construction of various biologically important quinoxalin-2(1H)-one backbones.
The first general, highly enantioselective lewis base organocatalyzed hydrosilylation of benzoxazinones and quinoxalinones
Xue, Zhou-Yang,Jiang, Yan,Peng, Xiao-Zhi,Yuan, Wei-Cheng,Zhang, Xiao-Mei
supporting information; experimental part, p. 2132 - 2136 (2010/11/04)
The first general, highly enantioselective hydrosilylation of benzoxazinones and quinoxalinones has been developed. The chiral Lewis base organocatalysis that are readily accessible from (1S,2R)-ephedrine and (1R,2S)-ephedrine promoted the title reaction to afford various chiral dihydrobenzoxazinones and dihydroquinoxalinones with good yields as well as good enantioselectivities.
