Nature Communications (Sep 2016)

Boron-mediated sequential alkyne insertion and C–C coupling reactions affording extended π-conjugated molecules

  • Yoshiaki Shoji,
  • Naoki Tanaka,
  • Sho Muranaka,
  • Naoki Shigeno,
  • Haruka Sugiyama,
  • Kumiko Takenouchi,
  • Fatin Hajjaj,
  • Takanori Fukushima

DOI
https://doi.org/10.1038/ncomms12704
Journal volume & issue
Vol. 7, no. 1
pp. 1 – 7

Abstract

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Coupling reactions to form C–C bonds typically require transition metals. Here the authors report that an organoboron compound can allow sequential alkyne insertion and unusual oxidative deborylation/Csp2 –Csp2 coupling, enabling the transformation of acetylenes into extended π-conjugated molecules.