Pd/C-catalyzed aerobic oxidative C-H alkenylation of arenes in γ-valerolactone (GVL)

被引:8
作者
Anastasiou, Ioannis [1 ]
Ferlin, Francesco [1 ]
Viteritti, Orlando [1 ]
Santoro, Stefano [1 ]
Vaccaro, Luigi [1 ]
机构
[1] Univ Perugia, Dipt Chim Biol & Biotecnol, Lab Green SOC, Via Elce di Sotto 8, I-06123 Perugia, Italy
来源
MOLECULAR CATALYSIS | 2021年 / 513卷
基金
欧盟地平线“2020”;
关键词
C-H alkenylation; Green solvents; Oxygen; Heterogeneous catalysis; Fujiwara-Moritani reaction; N BOND FORMATION; AROMATIC-SUBSTITUTION; OXIDASE CATALYSIS; MOLECULAR-OXYGEN; HIGHLY EFFICIENT; HECK REACTION; ACTIVATION; OLEFINS; FUNCTIONALIZATION; ANNULATION;
D O I
10.1016/j.mcat.2021.111787
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A novel methodology for the heterogeneous palladium-catalyzed C-H alkenylation of N-methoxybenzamides and anilides is presented. This approach is based on the use of commercially available Pd/C as catalyst and molecular oxygen as terminal oxidant, in combination with a substoichiometric amount of benzoquinone. Furthermore, the reaction can be conducted in non-toxic biomass-derived gamma-valerolactone (GVL) as reaction medium. The catalytic system exploited high activity leading to good isolated yields to several interesting products. In addition, the catalyst showed a remarkable stability in the reaction conditions, allowing its recycling in consecutive reaction runs.
引用
收藏
页数:7
相关论文
共 76 条
  • [1] Cobalt-Catalyzed C-H Arylations, Benzylations, and Alkylations with Organic Electrophiles and Beyond
    Ackermann, Lutz
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2014, 79 (19) : 8948 - 8954
  • [2] Carboxylate-Assisted Transition-Metal-Catalyzed C-H Bond Functionalizations: Mechanism and Scope
    Ackermann, Lutz
    [J]. CHEMICAL REVIEWS, 2011, 111 (03) : 1315 - 1345
  • [3] C2-H Arylation of Indoles Catalyzed by Palladium-Containing Metal-Organic-Framework in γ-Valerolactone
    Anastasiou, Ioannis
    Van Velthoven, Niels
    Tomarelli, Elena
    Lombi, Aurora
    Lanari, Daniela
    Liu, Pei
    Bals, Sara
    De Vos, Dirk E.
    Vaccaro, Luigi
    [J]. CHEMSUSCHEM, 2020, 13 (10) : 2786 - 2791
  • [4] Ruthenium(II) oxidase catalysis for C-H alkenylations in biomass-derived γ-valerolactone
    Bechtoldt, Alexander
    Baumert, Marcel E.
    Vaccaro, Luigi
    Ackermann, Lutz
    [J]. GREEN CHEMISTRY, 2018, 20 (02) : 398 - 402
  • [5] Ruthenium Oxidase Catalysis for Site-Selective C-H Alkenylations with Ambient O2 as the Sole Oxidant
    Bechtoldt, Alexander
    Tirler, Carina
    Raghuvanshi, Keshav
    Warratz, Svenja
    Kornhaass, Christoph
    Ackermann, Lutz
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2016, 55 (01) : 264 - 267
  • [6] Mild aerobic oxidative palladium (II) catalyzed C-H bond functionalization: Regioselective and switchable C-H alkenylation and annulation of pyrroles
    Beck, EM
    Grimster, NP
    Hatley, R
    Gaunt, MJ
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (08) : 2528 - 2529
  • [7] Selective Pd-catalyzed oxidative coupling of anilides with olefins through C-H bond activation at room temperature
    Boele, MDK
    van Strijdonck, GPF
    de Vries, AHM
    Kamer, PCJ
    de Vries, JG
    van Leeuwen, PWNM
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (08) : 1586 - 1587
  • [8] Continuous flow transfer hydrogenation of biomass derived methyl levulinate over Zr containing zeolites: Insights into the role of the catalyst acidity
    Cabanillas, Matilde
    Franco, Ana
    Lazaro, Noelia
    Balu, Alina M.
    Luque, Rafael
    Pineda, Antonio
    [J]. MOLECULAR CATALYSIS, 2019, 477
  • [9] Rh(III)-Catalyzed Cascade Oxidative Olefination/Cyclization of Picolinamides and Alkenes via C-H Activation
    Cai, Shangun
    Chen, Chao
    Shao, Peng
    Xi, Chanjuan
    [J]. ORGANIC LETTERS, 2014, 16 (11) : 3142 - 3145
  • [10] Polarclean/Water as a Safe and Recoverable Medium for Selective C2-Arylation of Indoles Catalyzed by Pd/C
    Campana, Filippo
    Massaccesi, Beatrice Maria
    Santoro, Stefano
    Piermatti, Oriana
    Vaccaro, Luigi
    [J]. ACS SUSTAINABLE CHEMISTRY & ENGINEERING, 2020, 8 (44): : 16441 - 16450