N,N-Dimethyl Glycine-Promoted Ullmann Coupling Reaction of Phenols and Aryl Halides

Dawei Ma* and Qian Cai
State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China
Org. Lett., 2003, 5 (21), pp 3799–3802
DOI: 10.1021/ol0350947
Publication Date (Web): September 26, 2003
Copyright © 2003 American Chemical Society
*

In papers with more than one author, the asterisk indicates the name of the author to whom inquiries about the paper should be addressed.

, madw@pub.sioc.ac.cn

Abstract

Abstract Image

Ullmann-type diaryl ether synthesis can be performed at 90 °C using either aryl iodides or aryl bromides as the substrates under the assistance of N,N-dimethylglycine.

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History

  • Published In Issue October 16, 2003
  • Received June 16, 2003
    Revised August 26, 2003

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