C-H functionalization enabled by multiple isocyanides

被引:5
|
作者
Gao, Mingchun [1 ]
Lu, Shaohang [1 ]
Xu, Bin [1 ,2 ,3 ]
机构
[1] Shanghai Univ, Peoples Hosp Nantong 6, Shanghai Engn Res Ctr Organ Repair, Dept Chem,Affiliated Nantong Hosp,Sch Med,Innovat, Shanghai 200444, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
[3] Shanghai Univ, Joint Int Res Lab Biomat & Biotechnol Organ Repair, Minist Educ, Shanghai 200444, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
HIGHLY REGIOSELECTIVE SYNTHESIS; PALLADIUM-CATALYZED SYNTHESIS; MU-ETHYNEDIYL COMPLEXES; CROSS-CYCLOADDITION; EFFICIENT SYNTHESIS; TERMINAL ALKYNES; DOUBLE INSERTION; MULTICOMPONENT REACTIONS; TRANSITION-METALS; ORGANIC-SYNTHESIS;
D O I
10.1039/d4cs00028e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Past decades have witnessed significant advance of isocyanides as a class of versatile organic synthons as well as their broad applications in multi-component reactions (MCRs) and other tandem reactions. Reactions involving multiple isocyanides allow the construction of molecules with further diversification and complexity, while C-H functionalization emphasizes the advantages of high atom economy, broad substrate availability and great synthetic efficiency. This promising synergistic strategy of C-H functionalization involving multiple isocyanides provides a variety of valuable synthetic methods for organic chemists' toolbox and offers considerable potential in pharmaceutical chemistry and materials science as well. The present review outlines in detail various reaction types of C-H functionalization enabled by multiple isocyanides, and the relevant mechanistic rationale is discussed. This review outlines in detail strategies for state-of-the-art synthetic routes and demonstrates various interactions from the synergistic combination of C-H functionalization with multiple isocyanides to establish the complicated reactions.
引用
收藏
页码:10147 / 10170
页数:24
相关论文
共 50 条
  • [1] Metal-catalyzed C-H functionalization involving isocyanides
    Song, Bingrui
    Xu, Bin
    CHEMICAL SOCIETY REVIEWS, 2017, 46 (04) : 1103 - 1123
  • [2] Electrochemical Benzylic C-H Functionalization with Isocyanides
    Tang, Shanyu
    Guillot, Regis
    Grimaud, Laurence
    Vitale, Maxime R.
    Vincent, Guillaume
    ORGANIC LETTERS, 2022, 24 (11) : 2125 - 2130
  • [3] C-H bond functionalization reactions enabled by photobiocatalytic cascades
    Li, Yuanying
    Yuan, Bo
    Sun, Zhoutong
    Zhang, Wuyuan
    GREEN SYNTHESIS AND CATALYSIS, 2021, 2 (03): : 267 - 274
  • [4] Transient Ligand-Enabled Transition Metal-Catalyzed C-H Functionalization
    Niu, Ben
    Yang, Ke
    Lawrence, Brianna
    Ge, Haibo
    CHEMSUSCHEM, 2019, 12 (13) : 2955 - 2969
  • [5] Multiple Catalytic C-H Bond Functionalization for Natural Product Synthesis
    Baudoin, Olivier
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2020, 59 (41) : 17798 - 17809
  • [6] A Sustainable Access Route to Carbazoles via C-H/C-H Oxidative Functionalization/Cyclization of Arylamines
    Brufani, Giulia
    Chen, Shaomin
    Di Erasmo, Benedetta
    Afanasenko, Anastasiia
    Gu, Yanlong
    Li, Chao-Jun
    Vaccaro, Luigi
    ACS SUSTAINABLE CHEMISTRY & ENGINEERING, 2024, 12 (22): : 8562 - 8572
  • [7] Iron-Catalyzed C-H Functionalization Processes
    Cera, Gianpiero
    Ackermann, Lutz
    TOPICS IN CURRENT CHEMISTRY, 2016, 374 (05)
  • [8] Silver-Mediated Oxidative C-H/C-H Functionalization: A Strategy To Construct Polysubstituted Furans
    He, Chuan
    Guo, Sheng
    Ke, Jie
    Hao, Jing
    Xu, Huan
    Chen, Hongyi
    Lei, Aiwen
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (13) : 5766 - 5769
  • [9] Ligand and counteranion enabled regiodivergent C-H bond functionalization of naphthols with α-aryl-α-diazoesters
    Yu, Zhunzhun
    Li, Yongfeng
    Zhang, Peichao
    Liu, Lu
    Zhang, Junliang
    CHEMICAL SCIENCE, 2019, 10 (26) : 6553 - 6559
  • [10] Palladium-catalyzed enantioselective C-H functionalization via C-H palladation
    Zhan, Bei-Bei
    Jin, Liang
    Shi, Bing-Feng
    TRENDS IN CHEMISTRY, 2022, 4 (03): : 220 - 235