Synthesis of Dibenzotropones by Alkyne-Carbonyl Metathesis

J Org Chem. 2021 Nov 5;86(21):14420-14432. doi: 10.1021/acs.joc.1c01132. Epub 2021 Oct 28.

Abstract

Dibenzocycloheptanones (dibenzotropones) were prepared by Brønsted acid mediated intramolecular alkyne-carbonyl metathesis (ACM) reactions. The cyclization precursors are readily available by Sonogashira reaction of 2-bromobenzoyl chloride with terminal alkynes, followed by Suzuki reactions with benzaldehydes. The ACM reactions are highly modular and atom economic and allow for the construction of two regioisomeric series of dibenzotropones.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes*
  • Benzaldehydes*
  • Cyclization

Substances

  • Alkynes
  • Benzaldehydes