From Quaternary Carbon to Tertiary C(sp3)-Si and C(sp3)-Ge Bonds: Decyanative Coupling of Malononitriles with Chlorosilanes and Chlorogermanes Enabled by Ni/Ti Dual Catalysis

被引:7
作者
Chen, Zi-Hao [1 ,2 ]
Zheng, Yu-Qing [1 ,2 ]
Huang, Hong-Gui [1 ,2 ]
Wang, Ke-Hao [1 ,2 ]
Gong, Jun-Lin [1 ,2 ]
Liu, Wen-Bo [1 ,2 ,3 ]
机构
[1] Wuhan Univ, Hubei Res Ctr Fundamental Sci Chem, Engn Res Ctr Organosilicon Cpds & Mat, Hubei Key Lab Organ & Polymer Optoelect Mat,Minist, Wuhan 430072, Peoples R China
[2] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
C-H SILYLATION; NICKEL; HALIDES; ALKYL; ARYL; FUNCTIONALIZATION; ELECTROPHILES; EPOXIDES; ARENES; LIGAND;
D O I
10.1021/jacs.4c04495
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition-metal-catalyzed C-Si/Ge cross-coupling offers promising avenues for the synthesis of organosilanes/organogermanes, yet it is fraught with long-standing challenges. A Ni/Ti-catalyzed strategy is reported here, allowing the use of disubstituted malononitriles as tertiary C(sp(3)) coupling partners to couple with chlorosilanes and chlorogermanes, respectively. This method enables the catalytic cleavage of the C(sp(3))-CN bond of the quaternary carbon followed by the formation of C(sp(3))-Si/C(sp(3))-Ge bonds from ubiquitously available starting materials. The efficiency and generality are showcased by a broad scope for both of the coupling partners, therefore holding the potential to synthesize structurally diverse quaternary organosilanes and organogermanes that were difficult to access previously.
引用
收藏
页码:14445 / 14452
页数:8
相关论文
共 68 条
[1]  
[Anonymous], 1998, CHEM ORGANIC SILICON, V2
[2]  
Auner N., 2004, ORGANOSILICON CHEM
[3]   C(sp3)-Si Cross-Coupling [J].
Baehr, Susanne ;
Xue, Weichao ;
Oestreich, Martin .
ACS CATALYSIS, 2019, 9 (01) :16-24
[4]   Divergent titanium-mediated allylations with modulation by nickel or palladium [J].
Campana, Araceli G. ;
Bazdi, Btissam ;
Fuentes, Noelia ;
Robles, Rafael ;
Cuerva, Juan M. ;
Oltra, J. Enrique ;
Porcel, Susana ;
Echavarren, Antonio M. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (39) :7515-7519
[5]   Carbon-Germanium Bond Formation via Low-Valent Cobalt- Catalyzed Cross-Electrophile Coupling [J].
Chen, Haifeng ;
Zhu, Chen ;
Yue, Huifeng ;
Rueping, Magnus .
ACS CATALYSIS, 2023, 13 (10) :6773-6780
[6]   Rhodium-Catalyzed Intermolecular C-H Silylation of Arenes with High Steric Regiocontrol [J].
Cheng, Chen ;
Hartwig, John F. .
SCIENCE, 2014, 343 (6173) :853-857
[7]   Transition metal-catalyzed alkyl-alkyl bond formation: Another dimension in cross-coupling chemistry [J].
Choi, Junwon ;
Fu, Gregory C. .
SCIENCE, 2017, 356 (6334)
[8]   Silicon-Carbon Bond Formation via Nickel-Catalyzed Cross-Coupling of Silicon Nucleophiles with Unactivated Secondary and Tertiary Alkyl Electrophiles [J].
Chu, Crystal K. ;
Liang, Yufan ;
Fu, Gregory C. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2016, 138 (20) :6404-6407
[9]   Palladium-Catalyzed Cross-Coupling of Silyl Electrophiles with Alkylzinc Halides: A Silyl-Negishi Reaction [J].
Cinderella, Andrew P. ;
Vulovic, Bojan ;
Watson, Donald A. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2017, 139 (23) :7741-7744
[10]   Nickel-Catalyzed Cross-Electrophile C(sp3)-Si Coupling of Unactivated Alkyl Bromides with Vinyl Chlorosilanes [J].
Duan, Jicheng ;
Wang, Yuquan ;
Qi, Liangliang ;
Guo, Peng ;
Pang, Xiaobo ;
Shu, Xing-Zhong .
ORGANIC LETTERS, 2021, 23 (20) :7855-7859