Synthesis of Enantioenriched 1,2-cis Disubstituted Cycloalkanes by Convergent NiH Catalysis

被引:18
作者
Chen, Changpeng [1 ]
Guo, Wenqing [1 ]
Qiao, Deyong [1 ]
Zhu, Shaolin [1 ,2 ,3 ]
机构
[1] Nanjing Univ, Chem & Biomed Innovat Ctr ChemB, Sch Chem & Chem Engn, State Key Lab Coordinat Chem,Jiangsu Key Lab Adv O, Nanjing 210093, Peoples R China
[2] Henan Normal Univ, Sch Chem & Chem Engn, Xinxiang 453007, Peoples R China
[3] Shanghai Jiao Tong Univ, Shanghai Key Lab Mol Engn Chiral Drugs, Shanghai 200240, Peoples R China
基金
中国博士后科学基金;
关键词
Alkenes; Alkylation; Asymmetric Catalysis; Isomerization; Nickel; REMOTE; HYDROALKYLATION; OLEFINS; FUNCTIONALIZATION; HYDROARYLATION; CARBOXYLATION; HYDROCARBONS; ARYLATION; ALKENES; ALKYNES;
D O I
10.1002/anie.202308320
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Enantioenriched multi-substituted cycloalkanes constitute an essential class of compounds in pharmaceuticals, natural products and agrochemicals. Here we report an NiH-catalyzed asymmetric migratory hydroalkylation process for the efficient and selective construction of such compounds. Through a dynamic kinetic asymmetric transformation (DYKAT), easily accessible racemic and isomeric mixtures of cycloalkenes could be directly utilized as starting materials, convergently producing thermo-dynamically disfavored chiral 1,2-cis disubstituted cycloalkanes bearing vicinal stereocenters with high levels of regio-, diastereo- and enantioselectivity. In addition, prochiral cyclic alkenes can be also employed, and deliver chiral 1,2-cis disubstituted cycloalkanes through desymmetrization process.
引用
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页数:5
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