ChemBeads-Enabled Photoredox High-Throughput Experimentation Platform to Improve C(sp2)-C(sp3) Decarboxylative Couplings

被引:14
作者
Gesmundo, Nathan J. [1 ]
Tu, Noah P. [1 ]
Sarris, Kathy A. [1 ]
Wang, Ying [1 ]
机构
[1] AbbVie Inc, N Chicago, IL 60064 USA
来源
ACS MEDICINAL CHEMISTRY LETTERS | 2023年 / 14卷 / 14期
关键词
High-throughput experimentation; chemical-coated glass beads; ChemBeads; photoredox catalysis; C(sp2)-C(sp3) cross-coupling; decarboxylative coupling; parallel library synthesis; NICKEL CATALYSIS; MERGING PHOTOREDOX; ARYLATION; SALTS; BATCH;
D O I
10.1021/acsmedchemlett.2c00538
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Enthusiasm surrounding nickel/photoredox C(sp2)-C(sp3) cross-couplings is very high; however, these methods are sometimes challenged by complex drug-like substrates in discovery chemistry. In our hands this has been especially true of the decarboxylative coupling, which has lagged behind other photoredox couplings in internal adoption and success. Herein, the development of a photoredox high-throughput experimentation platform to optimize challenging C(sp2)-C(sp3) decar-boxylative couplings is described. Chemical-coated glass beads (Chem-Beads) and a novel parallel bead dispenser are used to expedite the high-throughput experimentation process and identify improved coupling conditions. In this report, photoredox high-throughput experimentation is utilized to dramatically improve low-yielding decarboxylative C(sp2)- C(sp3) couplings, and libraries, using conditions not previously identified in the literature.
引用
收藏
页码:521 / 529
页数:9
相关论文
共 50 条
  • [41] 16-Electron Nickel(0)-Olefin Complexes in Low-Temperature C(sp2)- C(sp3) Kumada Cross-Couplings
    Lutz, Sigrid
    Nattmann, Lukas
    Noethling, Nils
    Cornella, Josep
    [J]. ORGANOMETALLICS, 2021, 40 (14) : 2220 - 2230
  • [42] Photochemical C-H bond coupling for (hetero)aryl C(sp2)-C(sp3) bond construction
    Zhao, Yating
    Xia, Wujiong
    [J]. ORGANIC & BIOMOLECULAR CHEMISTRY, 2019, 17 (20) : 4951 - 4963
  • [43] Synergistic Merger of Ketone, Halogen Atom Transfer (XAT), and Nickel-Mediated C(sp3)-C(sp2) Cross-Electrophile Coupling Enabled by Light
    Tripathy, Alisha Rani
    Bisoyi, Akash
    Arya, P.
    Venugopal, Sreelakshmi
    Yatham, Veera Reddy
    [J]. ACS ORGANIC & INORGANIC AU, 2023, 4 (02): : 229 - 234
  • [44] Theoretical study on the concerted catalysis of Ir/Ni for amino radical transfer for C(sp2)-C(sp3) bond formation
    Li, Hui
    Zheng, He
    [J]. DALTON TRANSACTIONS, 2024, 53 (44) : 18047 - 18053
  • [45] Visible light-induced aerobic photooxidative cleavage of C(sp3)-C(sp2) σ-bonds of allylarenes
    Tang, Jinyu
    Zhao, Xi
    Ni, Jinxuan
    Huo, Yanping
    Gao, Yang
    Li, Xianwei
    Liu, Yan
    Maruoka, Keiji
    Chen, Qian
    [J]. ORGANIC CHEMISTRY FRONTIERS, 2024, 11 (22): : 6385 - 6392
  • [46] Selective Oxidative Decarbonylative Cleavage of Unstrained C(sp3)-C(sp2) Bond: Synthesis of Substituted Benzoxazinones
    Verma, Ajay
    Kumar, Sangit
    [J]. ORGANIC LETTERS, 2016, 18 (17) : 4388 - 4391
  • [47] Palladium-Catalyzed C(sp3)-Si Bonds Transformation for Constructing Trifluoropropyl (Hetero)arenes through C(sp3)-C(sp2) Cross-Coupling Reactions
    Liu Junjun
    Lu Taotao
    Ma Ping
    Zhao Qingyang
    Yee, Kwong Fuk
    [J]. CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2024, 44 (04) : 1319 - 1326
  • [48] Photoredox C(sp3)-C(sp2) Cross-Dehydrogenative Coupling of Xanthene with β-keto Moiety using MoS2 Quantum Dot (QD) Catalyst.
    Deore, Jiteshkumar P.
    De, Mrinmoy
    [J]. ADVANCED SYNTHESIS & CATALYSIS, 2022, 364 (17) : 3049 - 3058
  • [49] Intramolecular PdII-catalyzed dehydrogenative C(sp3)-C(sp2) coupling: an alternative to Pd0-catalyzed C(sp3)-H arylation from aryl halides?
    Pierre, Cathleen
    Baudoin, Olivier
    [J]. TETRAHEDRON, 2013, 69 (22) : 4473 - 4478
  • [50] Pd(II)-Catalyzed Chemoselective Acetoxylation of C(sp2)-H and C(sp3)-H Bonds in Tertiary Amides
    Vijaykumar, Muniyappa
    Punji, Benudhar
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2021, 86 (12) : 8172 - 8181