Cu-Catalyzed Synthesis of Benzoxazole with Phenol and Cyclic Oxime

被引:9
|
作者
Wang, Zheng-Hai [1 ]
Wang, Dong-Hui [1 ,2 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Organ Chem, Lab Synthet & Self Assembly Chem Organ Funct Mol, Univ Chinese Acad Sci, Shanghai 200032, Peoples R China
[2] Nanjing Univ Chinese Med, Dept Pharm, Nanjing 210023, Peoples R China
基金
国家重点研发计划;
关键词
DEHYDROGENATIVE AMINATION; BOND FUNCTIONALIZATION; EFFICIENT SYNTHESIS; H AMINATION; COPPER; CYCLIZATION; ALKYLATION; AMINES;
D O I
10.1021/acs.orglett.1c04322
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A Cu-catalyzed straightforward synthesis of benzoxazoles from free phenols and cyclic oxime esters is reported. The mild reaction conditions tolerate various electron-withdrawing and electron-donating functional groups on both substrates, affording benzoxazoles in moderate to good yields. With this protocol, largescale syntheses of Ezutromid and Flunoxaprofe in one or two steps are demonstrated. A catalytic mechanism, which includes Cu-catalyzed amination via inner-sphere electron transfer and consequent annulation, is proposed.
引用
收藏
页码:782 / 785
页数:4
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