Decarboxylative C(sp3)-N Cross-Coupling of Diacyl Peroxides with Nitrogen Nucleophiles
Zi-Liang Tang, Xuan-Hui Ouyang*, Ren-Jie Song and Jin-Heng Li*
*Key Laboratory of Jiangxi Province for Persistent Pollutants Control and Resources Recycle, Nanchang Hangkong University, Nanchang 330063, China, Email: xuanhuiouyang163.com, jhlihnu.edu.cn
Z. -L. Tang, X.-H. Ouyang, R.-J. Song, J.-H. Li, Org. Lett., 2021, 23, 1000-1004.
DOI: 10.1021/acs.orglett.0c04203
see article for more reactions
Abstract
A radical-mediated decarboxylative C(sp3)-N cross-coupling of diacyl peroxides with nitrogen nucleophiles, including indazoles, triazoles, indoles, and anilines provides a broad range of alkylated products. The primary and secondary alkyl radicals derived from corresponding diacyl peroxides were generated by copper catalysis or by merging copper catalysis and photoredox catalysis, respectively.
see article for more examples
Key Words
aryl amines, indazoles, N-heterocycles
ID: J54-Y2021