Pd-Catalyzed Cross-Couplings: On the Importance of the Catalyst Quantity Descriptors, mol % and ppm

被引:37
|
作者
Horbaczewskyj, Christopher S. [1 ]
Fairlamb, Ian J. S. [1 ]
机构
[1] Univ York, York YO10 5DD, North Yorkshire, England
基金
英国工程与自然科学研究理事会;
关键词
palladium; ppm palladium; cross-coupling; Suzuki-Miyaura; Kumada; Negishi; Stille; Heck; Sonogashira; cyanation; direct arylation; Buchwald-Hartwig amination cross-coupling; quantification; synthesis; catalysis; C-H ARYLATION; BUCHWALD-HARTWIG AMINATION; SUZUKI-MIYAURA COUPLINGS; ELECTRON-RICH OLEFINS; UNACTIVATED ARYL CHLORIDES; FREE SONOGASHIRA COUPLINGS; KUMADA-CORRIU COUPLINGS; NITRO-GROUP REDUCTIONS; CARBON BOND FORMATION; ONE-POT SYNTHESIS;
D O I
10.1021/acs.oprd.2c00051
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
ABSTRACT: This Review examines parts per million (ppm) palladium concentrations in catalytic cross-coupling reactions and their relationship with mole percentage (mol %). Most studies in catalytic cross-coupling chemistry have historically focused on the concentration ratio between (pre)catalyst and the limiting reagent (substrate), expressed as mol %. Several recent papers have outlined the use of "ppm level" palladium as an alternative means of describing catalytic cross-coupling reaction systems. This led us to delve deeper into the literature to assess whether "ppm level" palladium is a practically useful descriptor of catalyst quantities in palladium-catalyzed cross-coupling reactions. Indeed, we conjectured that many reactions could, unknowingly, have employed low "ppm levels" of palladium (pre)catalyst, and generally, what would the spread of ppm palladium look like across a selection of studies reported across the vast array of the cross-coupling chemistry literature. In a few selected examples, we have examined other metal catalyst systems for comparison with palladium.
引用
收藏
页码:2240 / 2269
页数:30
相关论文
共 50 条
  • [1] ppm-Level Pd-catalyzed cross-couplings in water at room temperature
    Lipshutz, Bruce
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2015, 249
  • [2] Deciphering complexity in Pd-catalyzed cross-couplings
    Clarke, George E.
    Firth, James D.
    Ledingham, Lyndsay A.
    Horbaczewskyj, Chris S.
    Bourne, Richard A.
    Bray, Joshua T. W.
    Martin, Poppy L.
    Eastwood, Jonathan B.
    Campbell, Rebecca
    Pagett, Alex
    Macquarrie, Duncan J.
    Slattery, John M.
    Lynam, Jason M.
    Whitwood, Adrian C.
    Milani, Jessica
    Hart, Sam
    Wilson, Julie
    Fairlamb, Ian J. S.
    NATURE COMMUNICATIONS, 2024, 15 (01)
  • [3] Pd-Catalyzed Decarbonylative Cross-Couplings of Aroyl Chlorides
    Malapit, Christian A.
    Ichiishi, Naoko
    Sanford, Melanie S.
    ORGANIC LETTERS, 2017, 19 (15) : 4142 - 4145
  • [4] Tris(trimethylsilyl)silanes and germanes in Pd-catalyzed cross-couplings
    Wang, ZZ
    Wnuk, SF
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2005, 230 : U3084 - U3084
  • [5] Mechanism of Cu/Pd-Catalyzed Decarboxylative Cross-Couplings: A DFT Investigation
    Fromm, Andreas
    van Wuellen, Christoph
    Hackenberger, Dagmar
    Goossen, Lukas J.
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2014, 136 (28) : 10007 - 10023
  • [6] Preparation of Solid Organozinc Pivalates and their Reaction in Pd-Catalyzed Cross-Couplings
    Ellwart, Mario
    Chen, Yi-Hung
    Tuellmann, Carl Phillip
    Malakhov, Vladimir
    Knochel, Paul
    ORGANIC SYNTHESES, 2018, 95 : 127 - +
  • [7] Mechanism of Cu/Pd-catalyzed decarboxylative cross-couplings: A DFT investigation
    Gooßen, L.J. (goossen@chemie.uni-kl.de), 1600, American Chemical Society (136):
  • [8] Pd-catalyzed decarboxylative cross-couplings of potassium malonate monoesters with aryl halides
    Feng, Yi-Si
    Wu, Wei
    Xu, Zhong-Qiu
    Li, Yan
    Li, Ming
    Xu, Hua-Jian
    TETRAHEDRON, 2012, 68 (09) : 2113 - 2120
  • [9] Atom-efficient Pd-catalyzed cross-couplings of chloroarenes with triarylbismuth reagents
    Rao, Maddali L. N.
    Meka, Suresh
    TETRAHEDRON LETTERS, 2019, 60 (34)
  • [10] Pd-catalyzed, cu(I)-mediated cross-couplings of bisarylthiocyclobutenediones with boronic acids and organostannanes
    Aguilar-Aguilar, Angelica
    Liebeskind, Lanny S.
    Pena-Cabrera, Eduardo
    JOURNAL OF ORGANIC CHEMISTRY, 2007, 72 (22): : 8539 - 8542