Unsymmetric N-Aryl Substituent Effects on Chiral NHC-Cu: Enantioselectivity and Reactivity Enhancement by Ortho-H and Syn-Configuration

Xi, Jianwei1,2,3; Ng, Elvis Wang Hei1,2,3,4; Ho, Chun-Yu1,2,3

2022-12-01

10.1021/acscatal.2c03942

ACS Catalysis   影响因子和分区

2155-5435

The N-aryl substituent effects on chiral C1 NHC's configuration and noncovalent interactions were studied by Cu catalyzed borylation. An inconspicuous N-aryl ortho-H, which can be found in many chiral C1 NHC designs, is now explored as a nonclassical hydrogen bonding site to achieve higher chiral induction ability. According to density functional theory (DFT) calculations, it cooperates with other noncovalent interactions, resulting in an unusual dual maxima shape e.r.-Hammett plot. A 2,6-unsymmetric substituted N-aryl on the other side also allowed for better chiral induction ability (similar to 3-fold e.r. increase) and higher relative reactivity (increase to 20:1). A catalyst with a syn- configuration between the NHC core Ph and the bulkier N-aryl o- substituent, which is supported by the crystal structures, the DFT calculations, and nuclear magnetic resonance (NMR), was found to be more effective than the more regularly hypothesized catalyst with an anti-configuration. A well-defined chiral NHC-Cu catalyst was then developed for highly enantioselective B-substituted quaternary center synthesis, which is effective for both E-/Z-enones (up to 98% e.e.) and substitution patterns with limited steric differences at beta-positions.

N-heterocyclic carbenes Cu catalysis enantioselective borylation chiral quaternary center noncovalent interactions insertions energy decomposition analysis

SCI ; EI

英语

第一 ; 通讯

Laboratory of Catalysis[2020B121201002] ; SUSTech["Y01501808","Y01506014"] ; NSFC[22071096]

Chemistry

Chemistry, Physical

WOS:000916650100001

AMER CHEMICAL SOC

20225213289159

Catalysis ; Copper compounds ; Crystal structure ; Density functional theory ; Enantioselectivity ; Hydrogen bonds ; Ions ; Nuclear magnetic resonance ; Organic compounds ; Substitution reactions

Physical Chemistry:801.4 ; Chemical Reactions:802.2 ; Chemical Agents and Basic Industrial Chemicals:803 ; Chemical Products Generally:804 ; Organic Compounds:804.1 ; Probability Theory:922.1 ; Atomic and Molecular Physics:931.3 ; Quantum Theory; Quantum Mechanics:931.4 ; Crystal Lattice:933.1.1

Web of Science

1.Southern Univ Sci & Technol SUSTech, Guangdong Prov Key Lab Catalysis, Shenzhen 518055, Peoples R China
2.Southern Univ Sci & Technol SUSTech, Shenzhen Grubbs Inst, Shenzhen 518055, Peoples R China
3.Southern Univ Sci & Technol SUSTech, Dept Chem, Shenzhen 518055, Peoples R China
4.Univ Hong Kong, Dept Chem, Hong Kong, Peoples R China

Xi, Jianwei,Ng, Elvis Wang Hei,Ho, Chun-Yu. Unsymmetric N-Aryl Substituent Effects on Chiral NHC-Cu: Enantioselectivity and Reactivity Enhancement by Ortho-H and Syn-Configuration[J]. ACS Catalysis,2022,13(1):407-421.

Xi, Jianwei,Ng, Elvis Wang Hei,&Ho, Chun-Yu.(2022).Unsymmetric N-Aryl Substituent Effects on Chiral NHC-Cu: Enantioselectivity and Reactivity Enhancement by Ortho-H and Syn-Configuration.ACS Catalysis,13(1),407-421.

Xi, Jianwei,et al."Unsymmetric N-Aryl Substituent Effects on Chiral NHC-Cu: Enantioselectivity and Reactivity Enhancement by Ortho-H and Syn-Configuration".ACS Catalysis 13.1(2022):407-421.