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Room temperature palladium catalysed coupling of acyl chlorides with terminal alkynes.
Chem Commun (Camb). 2005 Feb 28CC

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.

Authors+Show Affiliations

Cox RJ
School of Chemistry, University of Bristol, Cantock's Close, Bristol, UKBS8 1TS. r.j.cox@bris.ac.uk
Ritson DJ
No affiliation info available
Dane TA
No affiliation info available
Berge J
No affiliation info available
Charmant JP
No affiliation info available
Kantacha A
No affiliation info available

MeSH

AlkynesBenzoatesCatalysisCopperIodidesMolecular StructurePalladiumTemperature

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

15719108

Citation

Cox, Russell J., et al. "Room Temperature Palladium Catalysed Coupling of Acyl Chlorides With Terminal Alkynes." Chemical Communications (Cambridge, England), 2005, pp. 1037-9.
Cox RJ, Ritson DJ, Dane TA, et al. Room temperature palladium catalysed coupling of acyl chlorides with terminal alkynes. Chem Commun (Camb). 2005.
Cox, R. J., Ritson, D. J., Dane, T. A., Berge, J., Charmant, J. P., & Kantacha, A. (2005). Room temperature palladium catalysed coupling of acyl chlorides with terminal alkynes. Chemical Communications (Cambridge, England), (8), 1037-9.
Cox RJ, et al. Room Temperature Palladium Catalysed Coupling of Acyl Chlorides With Terminal Alkynes. Chem Commun (Camb). 2005 Feb 28;(8)1037-9. PubMed PMID: 15719108.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Room temperature palladium catalysed coupling of acyl chlorides with terminal alkynes. AU - Cox,Russell J, AU - Ritson,Dougal J, AU - Dane,Thomas A, AU - Berge,John, AU - Charmant,Jonathan P H, AU - Kantacha,Anob, Y1 - 2005/01/10/ PY - 2005/2/19/pubmed PY - 2007/3/22/medline PY - 2005/2/19/entrez SP - 1037 EP - 9 JF - Chemical communications (Cambridge, England) JO - Chem Commun (Camb) IS - 8 N2 - 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. SN - 1359-7345 UR - https://www.unboundmedicine.com/medline/citation/15719108/Room_temperature_palladium_catalysed_coupling_of_acyl_chlorides_with_terminal_alkynes_ DB - PRIME DP - Unbound Medicine ER -