Pd-catalyzed Suzuki-Miyaura cross-coupling of pentafluorophenyl esters

Jonathan Buchspies, Daniel J. Pyle, Huixin He, Michal Szostak

Research output: Contribution to journalArticlepeer-review

9 Scopus citations


Although the palladium-catalyzed Suzuki-Miyaura cross-coupling of aryl esters has received significant attention, there is a lack of methods that utilize cheap and readily accessible Pd-phosphane catalysts, and can be routinely carried out with high cross-coupling selectivity. Herein, we report the first general method for the cross-coupling of pentafluorophenyl esters (pentafluorophenyl = pfp) by selective C–O acyl cleavage. The reaction proceeds efficiently using Pd(0)/phosphane catalyst systems. The unique characteristics of pentafluorophenyl esters are reflected in the fully selective cross-coupling vs. phenolic esters. Of broad synthetic interest, this report establishes pentafluorophenyl esters as new, highly reactive, bench-stable, economical, ester-based, electrophilic acylative reagents via acyl-metal intermediates. Mechanistic studies strongly support a unified reactivity scale of acyl electrophiles by C(O)–X (X = N, O) activation. The reactivity of pfp esters can be correlated with barriers to isomerization around the C(acyl)–O bond.

Original languageEnglish (US)
Article number3134
Issue number12
StatePublished - Nov 29 2018

All Science Journal Classification (ASJC) codes

  • Drug Discovery
  • Analytical Chemistry
  • Chemistry (miscellaneous)
  • Molecular Medicine
  • Physical and Theoretical Chemistry
  • Pharmaceutical Science
  • Organic Chemistry


  • Aryl esters
  • Cross-coupling
  • C–O activation
  • Pd-catalysis
  • Suzuki-Miyaura

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