IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v8y2017i1d10.1038_ncomms14641.html
   My bibliography  Save this article

Palladium-catalysed synthesis of triaryl(heteroaryl)methanes

Author

Listed:
  • Shuguang Zhang

    (Roy and Diana Vagelos Laboratories, University of Pennsylvania)

  • Byeong-Seon Kim

    (Roy and Diana Vagelos Laboratories, University of Pennsylvania)

  • Chen Wu

    (Roy and Diana Vagelos Laboratories, University of Pennsylvania)

  • Jianyou Mao

    (Institute of Advanced Synthesis, School of Chemistry and Molecular Engineering, Jiangsu National Synergetic Innovation Center for Advanced Materials, Nanjing Tech University)

  • Patrick J. Walsh

    (Roy and Diana Vagelos Laboratories, University of Pennsylvania
    Institute of Advanced Synthesis, School of Chemistry and Molecular Engineering, Jiangsu National Synergetic Innovation Center for Advanced Materials, Nanjing Tech University)

Abstract

Tetraarylmethane derivatives are desirable for a variety of applications, but difficult to access with modern C–C bond-forming reactions. Here we report a straightforward method for palladium-catalysed arylation of aryl(heteroaryl)methanes and diaryl(heteroaryl)methanes with aryl chlorides. This reaction enables introduction of various aryl groups to construct triaryl(heteroaryl)methanes via a C–H functionalization in good to excellent yield, and represents the first step towards a general transition metal catalysed synthesis of tetraarylmethanes.

Suggested Citation

  • Shuguang Zhang & Byeong-Seon Kim & Chen Wu & Jianyou Mao & Patrick J. Walsh, 2017. "Palladium-catalysed synthesis of triaryl(heteroaryl)methanes," Nature Communications, Nature, vol. 8(1), pages 1-8, April.
  • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms14641
    DOI: 10.1038/ncomms14641
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/ncomms14641
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/ncomms14641?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms14641. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.