Metal-Free Transformation of Sulfonyl Oxime Ethers with Amines to Oxime Ethers

被引:6
|
作者
Zhang, Jia-Yuan [1 ]
Hu, Jinglin [1 ]
Li, Xiao-Xuan [1 ]
Tang, Wei-Ke [1 ]
Feng, Yi-Si [1 ,2 ]
机构
[1] Hefei Univ Technol, Sch Chem & Chem Engn, Anhui Prov Key Lab Adv Catalyt Mat & React Engn S, Hefei 230009, Peoples R China
[2] Anhui Prov Lab Heterocycl Chem, Maanshan 243110, Peoples R China
来源
JOURNAL OF ORGANIC CHEMISTRY | 2021年 / 86卷 / 18期
基金
中国国家自然科学基金;
关键词
C-H ARYLATION; N-ALKOXYIMIDOYL BROMIDES; IN-SITU; ASYMMETRIC-SYNTHESIS; VISIBLE-LIGHT; ASCORBIC-ACID; (HETERO)ARENES; PHOTOREDOX; REDUCTION; DONORS;
D O I
10.1021/acs.joc.1c01197
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Sulfonyl oxime ethers undergo facile radical substitutions with various amines to yield the corresponding oxime ethers. An efficient arylation of sulfonyl oxime ethers was accomplished under ambient temperature and metal-free conditions, with a wide range of functional group tolerance. Mechanistic investigations indicate that a phenyl radical is involved in the catalytic cycle.
引用
收藏
页码:12676 / 12682
页数:7
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