IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v7y2016i1d10.1038_ncomms11698.html
   My bibliography  Save this article

Fast, greener and scalable direct coupling of organolithium compounds with no additional solvents

Author

Listed:
  • Erik B. Pinxterhuis

    (Faculty of Mathematics and Natural Sciences, Stratingh Institute for Chemistry, University of Groningen)

  • Massimo Giannerini

    (Faculty of Mathematics and Natural Sciences, Stratingh Institute for Chemistry, University of Groningen)

  • Valentín Hornillos

    (Faculty of Mathematics and Natural Sciences, Stratingh Institute for Chemistry, University of Groningen)

  • Ben L. Feringa

    (Faculty of Mathematics and Natural Sciences, Stratingh Institute for Chemistry, University of Groningen)

Abstract

Although the use of catalytic rather than stoichiometric amounts of metal mediator in cross-coupling reactions between organic halides and organometallic counterparts improves significantly the atom economy and waste production, the use of solvents and stoichiometric generation of main-group byproducts (B, Sn and Zn) hamper the ‘greenness’ and industrial efficiency of these processes. Here we present a highly selective and green Pd-catalysed cross-coupling between organic halides and organolithium reagents proceeding without additional solvents and with short reaction times (10 min). This method bypasses a number of challenges previously encountered in Pd-catalysed cross-coupling with organolithium compounds such as strict exclusion of moisture, dilution and slow addition. Operational ease of this protocol combines the use of industrially viable catalysts loadings (down to 0.1 mol%), scalability of the process (tested up to 120 mmol) and exceptionally favourable environmental impact (E factors in several cases as low as 1).

Suggested Citation

  • Erik B. Pinxterhuis & Massimo Giannerini & Valentín Hornillos & Ben L. Feringa, 2016. "Fast, greener and scalable direct coupling of organolithium compounds with no additional solvents," Nature Communications, Nature, vol. 7(1), pages 1-7, September.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms11698
    DOI: 10.1038/ncomms11698
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/ncomms11698
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/ncomms11698?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:7:y:2016:i:1:d:10.1038_ncomms11698. 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.