Room temperature palladium catalysed coupling of acyl chlorides with terminal alkynes

Research output: Contribution to journalArticleResearchpeer review

Authors

  • Russell J. Cox
  • Dougal J. Ritson
  • Thomas A. Dane
  • John Berge
  • Jonathan P.H. Charmant
  • Anob Kantacha

External Research Organisations

  • University of Bristol
  • GlaxoSmithKline GmbH and Co. KG
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Details

Original languageEnglish
Pages (from-to)1037-1039
Number of pages3
JournalChemical communications
Issue number8
Publication statusPublished - 28 Feb 2005
Externally publishedYes

Abstract

Conditions are reported for the facile, high-yielding coupling of acyl chlorides with terminal alkynes in a reaction involving palladium and copper iodide; the reaction is tolerant of a wide variety of acyl chlorides and terminal alkynes and provides a convenient one-pot route to acetylenic ketones.

ASJC Scopus subject areas

Cite this

Room temperature palladium catalysed coupling of acyl chlorides with terminal alkynes. / Cox, Russell J.; Ritson, Dougal J.; Dane, Thomas A. et al.
In: Chemical communications, No. 8, 28.02.2005, p. 1037-1039.

Research output: Contribution to journalArticleResearchpeer review

Cox, R. J., Ritson, D. J., Dane, T. A., Berge, J., Charmant, J. P. H., & Kantacha, A. (2005). Room temperature palladium catalysed coupling of acyl chlorides with terminal alkynes. Chemical communications, (8), 1037-1039. https://doi.org/10.1039/b414826f
Cox RJ, Ritson DJ, Dane TA, Berge J, Charmant JPH, Kantacha A. Room temperature palladium catalysed coupling of acyl chlorides with terminal alkynes. Chemical communications. 2005 Feb 28;(8):1037-1039. doi: 10.1039/b414826f
Cox, Russell J. ; Ritson, Dougal J. ; Dane, Thomas A. et al. / Room temperature palladium catalysed coupling of acyl chlorides with terminal alkynes. In: Chemical communications. 2005 ; No. 8. pp. 1037-1039.
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