Pd-catalyzed copper-free carbonylative Sonogashira reaction of aryl iodides with alkynes for the synthesis of alkynyl ketones and flavones by using water as a solvent

B Liang, M Huang, Z You, Z Xiong, K Lu…

Index: Liang, Bo; Huang, Mengwei; You, Zejin; Xiong, Zhengchang; Lu, Kui; Fathi, Reza; Chen, Jiahua; Yang, Zhen Journal of Organic Chemistry, 2005 , vol. 70, # 15 p. 6097 - 6100

Full Text: HTML

Citation Number: 133

Abstract

The Pd-catalyzed copper-free carbonylative Sonogashira coupling reaction to synthesize alkynyl ketones from terminal alkynes and aryl iodides was achieved by using water as a solvent. The reaction was carried out at room temperature under balloon pressure of CO with Et3N as a base. The developed method was successfully applied to the synthesis of flavones.

Related Articles:

Pd-catalyzed coupling reaction of acid chlorides with terminal alkynes using 1-(2-pyridylethynyl)-2-(2-thienylethynyl) benzene ligand

[Atobe, Shingo; Masuno, Haruna; Sonoda, Motohiro; Suzuki, Yuki; Shinohara, Hiroyuki; Shibata, Satoshi; Ogawa, Akiya Tetrahedron Letters, 2012 , vol. 53, # 14 p. 1764 - 1767]

More Articles...