期刊
ADVANCED SYNTHESIS & CATALYSIS
卷 359, 期 9, 页码 1515-1521出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201700070
关键词
arylhydrazines; benzo[g]quinoxalinones; iodosylbenzene (PHIO)-promoted reaction; pyrido[3; 4-b]pyrazinones; transition metal-free oxidative arylation
资金
- National Research Foundation of Korea (NRF) - Korea government (MSIP) [NRF-2014R1A2A1A11052391]
- Nano Material Technology Development Program [2012M3A7B4049675]
A transition metal-free iodosobenzene-promoted direct oxidative 3-arylation of quinoxalin-2(H)-ones was developed using various arylhydrazines under air. The protocol affords a variety of 3-arylquinoxalin-2(H)-one derivatives in moderate to good yields. This method provides a rapid access to biologically interesting benzo[g]quinoxalinones and pyrido[3,4-b]pyrazinones. The present methodology features high functional group tolerance including base-sensitive groups as well as allyl- and benzyl-substituted quinoxalin-2(H)-ones under mild reaction conditions.
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