Synlett

Dimethylaminomethylphosphonic acid derivatives-promoted CuI-catalyzed synthesis of aryl ethers

Y Jin, J Liu, Y Yin, H Fu, Y Jiang, Y Zhao

Index: Jin, Ying; Liu, Jinyong; Yin, Yingwu; Fu, Hua; Jiang, Yuyang; Zhao, Yufen Synlett, 2006 , # 10 p. 1564 - 1568

Full Text: HTML

Citation Number: 13

Abstract

Abstract An inexpensive and efficient catalyst system for synthesis of aryl ethers has been developed by using 20 mol% CuI as the catalyst, 30 mol% dimethylaminomethylphosphonic acid derivatives as the new ligands, K 2 CO 3 as the base and toluene as the solvent. This is the first example using aminophosphonates as the ligands for Ullmann ether coupling reaction.

Related Articles:

Metal??Free Arylation of Oxygen Nucleophiles with Diaryliodonium Salts

[Jalalian, Nazli; Petersen, Tue B.; Olofsson, Berit Chemistry--A European Journal, 2012 , vol. 18, # 44 p. 14140 - 14149,10]

Selective One??Pot Access to Symmetrical or Unsymmetrical Diaryl Ethers by Copper??Catalyzed Double Arylation of a Simple Oxygen Source

[Tlili, Anis; Monnier, Florian; Taillefer, Marc Chemistry - A European Journal, 2010 , vol. 16, # 41 p. 12299 - 12302]

Regioselective conversion of arylboronic acids to phenols and subsequent coupling to symmetrical diaryl ethers

[Simon; Salzbrunn; Surya Prakash; Petasis; Olah Journal of Organic Chemistry, 2001 , vol. 66, # 2 p. 633 - 634]

Electrochemical fluorination of aromatic compounds in anhydrous HF

[Shainyan; Danilevich Russian Journal of Organic Chemistry, 2006 , vol. 42, # 2 p. 214 - 219]

More Articles...