Striving to exploit alkyl electrophiles: challenge and choice in transition metal-catalyzed cross-coupling reactions of sulfones

被引:8
|
作者
Liu, Mengli [1 ]
Zheng, Yannan [1 ]
Qiu, Guanyinsheng [1 ,2 ]
Wu, Jie [2 ,3 ]
机构
[1] Jiaxing Univ, Coll Biol Chem Sci & Engn, 118 Jiahang Rd, Jiaxing 314001, Peoples R China
[2] Fudan Univ, Dept Chem, 220 Handan Rd, Shanghai 200433, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, 345 Lingling Rd, Shanghai 200032, Peoples R China
来源
ORGANIC CHEMISTRY FRONTIERS | 2018年 / 5卷 / 17期
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
ALLYLIC GRIGNARD-REAGENTS; QUATERNARY CARBONS; HALIDES; TERTIARY; DERIVATIVES; STEREOCENTERS; ALLYLATION; CENTERS;
D O I
10.1039/c8qo00632f
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
For cross-coupling reactions of alkyl electrophiles, alkyl halides, alkyl tosylates, alkyl acetates and alkyl sulfones exhibit high reaction efficiency when various transition metal catalysts and reaction partners are employed. As crystalline and readily available alkyl electrophiles, alkyl sulfones in radical cross-coupling reactions open a new avenue for modularly generating diverse alkyl compounds. It is believed that more transformations using sulfones as electrophiles will be developed in the near future.
引用
收藏
页码:2615 / 2617
页数:3
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