文献类型：期刊文献

中文题名：Quinim配体的探索及其在镍催化烯烃的不对称胺甲酰基-烷基化反应的应用

英文题名：Exploration of Quinim Ligand in Ni-Catalyzed Enantioselective Reductive Carbamoyl-Alkylation of Alkene

作者：吴利城[1];伍贤青[1];曲景平[1];陈宜峰[1]

机构：[1]华东理工大学化学与分子工程学院、费林加诺贝尔奖科学家联合研究中心、材料生物学与动态化学前沿科学中心,上海200237

年份：2023

卷号：43

期号：12

起止页码：4239

中文期刊名：有机化学

外文期刊名：Chinese Journal of Organic Chemistry

收录：CSTPCD;;Scopus;WOS:【SCI-EXPANDED(收录号:WOS:001163473600014)】；北大核心:【北大核心2020】；CSCD:【CSCD2023_2024】；

基金：Project supported by the National Natural Science Foundation of China (No. 22171079), the Natural Science Foundation of Shanghai (No. 21ZR1480400), the Shanghai Rising-Star Program (No. 20QA1402300), the Shanghai Municipal Science and Technology Major Project (No. 2018SHZDZX03), the Program of Introducing Talents of Discipline to Universities (No. B16017), the China Postdoctoral Science Foundation (No. 2021M701197), the Shanghai Sailing Program (No. 23YF1408800) and the Fundamental Research Funds for the Central Universities.

语种：中文

中文关键词：Quinim配体;镍催化剂;季碳手性中心;γ-内酰胺

外文关键词：Quinim ligand;nickel catalysis;quaternary stereocenters;γ-lactam

摘要：发展手性配体是不对称催化的核心任务之一.本工作报道了镍催化1,1-二取代烯烃衍生的胺甲酰氯与烷基碘代物的不对称还原胺甲酰基-烷基化反应,构建了一系列对映选择性富集的α,α-双烷基取代的吡咯烷酮化合物.通过对Quinim配体的广泛探索,发现p-tolQuinim至1-NapQuinim配体的革新是该反应成功的关键,能以高收率、高对映选择性及出色的官能团容忍性得到多样的α-位含有季碳中心的γ-内酰胺化合物.此外,研究发现,新发展的Ni/1-NapQuinim催化体系也能提高α-单烷基取代γ-内酰胺的合成效率及对映选择性.
The development of new chiral ligand constitutes the cornerstone of asymmetric catalysis.An asymmetric synthesis ofα,α-dialkylated pyrrolidinones enabled by Ni-catalyzed reductive carbamoyl-alkylation of 1,1-disubstituted alkenetethered carbamoyl chlorides and primary alkyl iodides is presented.After extensive investigation of Quinim ligands,it is found that the evolution of chiral ligand p-tolQuinim to 1-NapQuinim is critical for formation of the all-carbon quaternary center in high yield and enantioselectivity and broad functional group tolerance.The newly developed catalytic system that combines nickel salts and the 1-NapQuinim ligand also improves both the yield and enantioselectivity in the synthesis ofα-monoalkylatedγ-lactams.