Talk:Carbon–hydrogen bond activation

Latest comment: 7 years ago by InternetArchiveBot in topic External links modified

External links modified edit

Hello fellow Wikipedians,

I have just modified one external link on Carbon–hydrogen bond activation. Please take a moment to review my edit. If you have any questions, or need the bot to ignore the links, or the page altogether, please visit this simple FaQ for additional information. I made the following changes:

When you have finished reviewing my changes, please set the checked parameter below to true or failed to let others know (documentation at {{Sourcecheck}}).

This message was posted before February 2018. After February 2018, "External links modified" talk page sections are no longer generated or monitored by InternetArchiveBot. No special action is required regarding these talk page notices, other than regular verification using the archive tool instructions below. Editors have permission to delete these "External links modified" talk page sections if they want to de-clutter talk pages, but see the RfC before doing mass systematic removals. This message is updated dynamically through the template {{source check}} (last update: 18 January 2022).

  • If you have discovered URLs which were erroneously considered dead by the bot, you can report them with this tool.
  • If you found an error with any archives or the URLs themselves, you can fix them with this tool.

Cheers.—InternetArchiveBot (Report bug) 01:01, 15 November 2016 (UTC)Reply

Check in a statement of Historical Overview edit

The statement "the first transition metal-mediated intermolecular C–H activation of unactivated and completely saturated hydrocarbons by oxidative addition" must be revised. Shilov system seems to be the first one.

Bibliography: Crabtree, R. H. Alkane C-H Activation and Functionalization with Homogeneous Transition Metal Catalysts: A Century of Progress - A New Millennium in Prospect. J. Chem. Soc. Dalt. Trans. 2001, No. 17, 2437–2450.

Quote of the bibliography: "Even though these results were mostly either ignored or met with disbelief at first, they can now be seen as the origin of the organometallic class of alkane oxidations." (pag. 2442)