I2-Mediated Site-Selective C-H Functionalization: Access to p-Amino-Substituted Unsymmetrical Benzils and Quinoxalines from Sulfoxonium Ylides

被引:3
|
作者
Saini, Rahul Kumar [1 ]
Borpatra, Paran J. [1 ]
Chaubey, Trayambek Nath [1 ]
Pandey, Satyendra Kumar [1 ]
机构
[1] Banaras Hindu Univ, Inst Sci, Dept Chem, Varanasi 221005, Uttar Pradesh, India
来源
JOURNAL OF ORGANIC CHEMISTRY | 2024年 / 89卷 / 08期
关键词
ONE-POT SYNTHESIS; METHYL KETONES; CATALYZED OXIDATION; EFFICIENT SYNTHESIS; ORTHO-HALOGENATION; ALPHA-KETOAMIDES; IN-VITRO; ANILINES; DERIVATIVES; ALKYNES;
D O I
10.1021/acs.joc.3c02975
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An I2-mediated approach for selective C-H functionalization of unprotected aniline derivatives for synthesizing benzils and quinoxaline derivatives from sulfoxonium ylides has been described. Aniline derivatives and sulfoxonium ylides ornamented with different functional groups showed good compatibility. They afforded the corresponding products with moderate to high yields via a mild and simple procedure. Finally, we validated the practicality of this method by scaling up the reaction and further conversion of the synthesized derivatives into other valuable molecules.
引用
收藏
页码:5536 / 5545
页数:10
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