Visible-light-mediated cobaloxime-catalyzed isomerization and hydroalkenylation of bicyclo[1.1.0]butanes

被引:0
|
作者
Mao, Ben [1 ,2 ]
Jiang, Sheng-Hao [1 ,2 ]
Xiong, Zheng [1 ,2 ]
Wei, Yin [3 ]
Shi, Min [1 ,2 ,3 ]
机构
[1] East China Univ Sci & Technol, Key Lab Adv Mat, 130 Meilong Rd, Shanghai 200237, Peoples R China
[2] East China Univ Sci & Technol, Inst Fine Chem, Sch Chem & Mol Engn, 130 Meilong Rd, Shanghai 200237, Peoples R China
[3] Chinese Acad Sci, Univ Chinese Acad Sci, Shanghai Inst Organ Chem, Ctr Excellence Mol Synth, 345 Lingling Rd, Shanghai 200032, Peoples R China
来源
ORGANIC CHEMISTRY FRONTIERS | 2025年 / 12卷 / 06期
基金
中国国家自然科学基金;
关键词
HYDROGEN; SYSTEM;
D O I
10.1039/d5qo00020c
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Bicyclo[1.1.0]butanes have received extensive attention from chemists in recent years and diverse approaches to access transformations of such strained molecules have been explored. Although cobalt catalysis has become a promising field in organic synthesis, the cobalt-catalyzed strain-release strategy of bicyclobutanes is still underdeveloped. Herein, we disclose a visible-light-driven cobaloxime-catalyzed protocol for bicyclo[1.1.0]butane transformations. A range of cyclobutene and alkenylated cyclobutane products have been obtained in moderate to excellent yields with excellent functional group tolerance. Synthetic applications of this protocol were conducted with several transformations. Moreover, a series of control experiments and spectroscopic experiments were performed to demonstrate the reaction mechanism.
引用
收藏
页码:1958 / 1965
页数:8
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