Synthesis of CF3-substituted isoindolones via rhodium(III)-catalyzed carbenoid C-H functionalization of aryl hydroxamates

被引:4
|
作者
Vorobyeva, Daria V. [1 ]
Bubnova, Alexandra S. [1 ]
Buyanovskaya, Anastasiya G. [1 ]
Osipov, Sergey N. [1 ]
机构
[1] Russian Acad Sci, A N Nesmeyanov Inst Organoelement Cpds, Moscow 119991, Russia
基金
俄罗斯科学基金会;
关键词
aryl hydroxamates; C-H activation; diazo compounds; rhodium(III) catalysis; isoindolones; organofluorine compounds; ACID-DERIVATIVES; CYCLOADDITION; ACCESS; ISOINDOLINONES; INHIBITORS; ALKENES;
D O I
10.1016/j.mencom.2023.01.010
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An efficient method for the selective preparation of trifluoro-methyl-substituted isoindolones has been developed via Rh-III-catalyzed C-H activation/[4 + 1]-annulation of aryl hydroxamates with functionalized acceptor/acceptor diazo compounds as cross-coupling partners.
引用
收藏
页码:34 / 36
页数:3
相关论文
共 50 条
  • [31] Rhodium(III)-Catalyzed Synthesis of Naphthols via C-H Activation of Sulfoxonium Ylides
    Xu, Youwei
    Yang, Xifa
    Zhou, Xukai
    Kong, Lingheng
    Li, Xingwei
    ORGANIC LETTERS, 2017, 19 (16) : 4307 - 4310
  • [32] Cascade Synthesis of 3-Alkylidene Dihydrobenzofuran Derivatives via Rhodium(III)-Catalyzed Redox-Neutral C-H Functionalization/Cyclization
    Zhou, Zhi
    Liu, Guixia
    Chen, Yan
    Lu, Xiyan
    ORGANIC LETTERS, 2015, 17 (23) : 5874 - 5877
  • [33] Synthesis of 2-Substituted Quinolines via Rhodium(III)-Catalyzed C-H Activation of Imidamides and Coupling with Cyclopropanols
    Zhou, Xukai
    Qi, Zisong
    Yu, Songjie
    Kong, Lingheng
    Li, Yang
    Tian, Wan-Fa
    Li, Xingwei
    ADVANCED SYNTHESIS & CATALYSIS, 2017, 359 (10) : 1620 - 1625
  • [34] Enantioselective Synthesis of Spiroindenes by Enol-Directed Rhodium(III)-Catalyzed C-H Functionalization and Spiroannulation
    Chidipudi, Suresh Reddy
    Burns, David J.
    Khan, Imtiaz
    Lam, Hon Wai
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2015, 54 (47) : 13975 - 13979
  • [35] Natural scaffolds-inspired synthesis of CF3-substituted macrolides enabled by Rh-catalyzed C-H alkylation macrocyclization
    Bi, Tongyu
    Xu, Yi
    Xu, Xin
    Tang, Bixi
    Yang, Qing
    Zang, Yi
    Lin, Zhenyang
    Li, Jia
    Yang, Weibo
    CHINESE CHEMICAL LETTERS, 2022, 33 (04) : 2015 - 2020
  • [36] Arylation of heterocycles via rhodium-catalyzed C-H bond functionalization
    Lewis, JC
    Wiedemann, SH
    Bergman, RG
    Ellman, JA
    ORGANIC LETTERS, 2004, 6 (01) : 35 - 38
  • [37] An Ir(III)-catalyzed aryl C-H bond carbenoid functionalization cascade: access to 1,3-dihydroindol-2-ones
    Bai, Siyi
    Chen, Xun
    Hu, Xinwei
    Deng, Yuanfu
    Jiang, Huanfeng
    Zeng, Wei
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2017, 15 (17) : 3638 - 3647
  • [38] Rhodium(III)-catalyzed indole-directed carbenoid aryl C-H insertion/cyclization: access to 1,2-benzocarbazoles
    Zhang, Zhenhui
    Liu, Kunkun
    Chen, Xun
    Su, Shi-Jian
    Deng, Yuanfu
    Zeng, Wei
    RSC ADVANCES, 2017, 7 (49): : 30554 - 30558
  • [39] Rhodium(III) Catalyzed C(p3)-H Functionalization
    Han Gaoxu
    Xu Hongtao
    Hou Wei
    CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2022, 42 (02) : 391 - 423
  • [40] Iron(III)-Catalyzed Regioselective Synthesis of Electron-Rich Benzothiazoles from Aryl Isothiocyanates via C-H Functionalization
    Srinivas, Bokka
    Shakeena, Kotari
    Kota, Durgeswari Lakkavarapu
    Abhinav, Valeti
    Eswar, Pyla
    Sravani, Rongali Geetha
    Kumar, Anandam Sampath Pavan
    Indukuri, Kiran
    Dhanaraju, Kumpatla Ayyappa
    Kumar, Muthyala Murali Krishna
    Alla, Santhosh Kumar
    JOURNAL OF ORGANIC CHEMISTRY, 2023, 88 (07): : 4458 - 4471