Thathagar Mehul B, Rothenberg Gadi
van't Hoff Institute for Molecular Sciences, University of Amsterdam, Nieuwe Achtergracht 166, 1018 WV, Amsterdam, The Netherlands.
Org Biomol Chem. 2006 Jan 7;4(1):111-5. doi: 10.1039/b513450a. Epub 2005 Nov 23.
The advantages of combining heterogeneous catalysis and aryl chloride substrates for cross-coupling are introduced. A heterogeneous Pd/C catalyst is used for activating aryl bromides and electron withdrawing aryl chlorides via a one-pot 'domino' HALEX-Sonogashira reaction. No ligand or co-catalyst is required, and the cross-coupling products are obtained in moderate to good yields. The influence of the solvent, base, iodide source and catalyst is evaluated. The catalyst is reusable for at least six consecutive reaction cycles. A variation on this reaction using catalytic amounts of KI is also proposed.
介绍了将多相催化与芳基氯底物用于交叉偶联的优点。一种多相Pd/C催化剂用于通过一锅法“多米诺”HALEX- Sonogashira反应活化芳基溴化物和吸电子芳基氯。无需配体或助催化剂,交叉偶联产物的收率为中等至良好。评估了溶剂、碱、碘化物源和催化剂的影响。该催化剂可重复使用至少六个连续反应循环。还提出了使用催化量的KI对该反应进行的改进。