37413-49-3

Upstream product

• 1196-57-2 quinoxalin-2⁽¹⁾-one 
• 6479-18-1 1-methyl-2(1H)-quinoxalinone 
• 5720-06-9 2-Methoxyphenylboronic acid 
• 27993-89-1 3-(2-methoxy-phenyl)-1H-quinoxalin-2-one 

Downstream Products

• 1255772-62-3 3-(2-methoxyphenyl)-1-methyl-3,4-dihydroquinoxalin-2(1H)-one 

Relevant academic research and scientific papers

Palladium(II)-catalyzed oxidative arylation of quinoxalin-2(1 H)-ones with arylboronic acids

A straightforward palladium-catalyzed oxidative C-3 arylation of quinoxalin-2(1H)-ones with arylboronic acids is reported. This 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

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.