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Gold(III) Chloride/Silver Triflate: A Highly Efficient Catalyst for Ring-Opening Reaction of Aziridines with Electron-Rich Arenes

  1. Xiaoyu Sun1,
  2. Wei Sun1,
  3. Renhua Fan1,
  4. Jie Wu1,2

Article first published online: 6 SEP 2007

DOI: 10.1002/adsc.200700101

Issue

Advanced Synthesis & Catalysis

Advanced Synthesis & Catalysis

Volume 349, Issue 13, pages 2151–2155, September 3, 2007

Additional Information

How to Cite

Sun, X., Sun, W., Fan, R. and Wu, J. (2007), Gold(III) Chloride/Silver Triflate: A Highly Efficient Catalyst for Ring-Opening Reaction of Aziridines with Electron-Rich Arenes. Adv. Synth. Catal., 349: 2151–2155. doi: 10.1002/adsc.200700101

Author Information

  1. 1

    Department of Chemistry, Fudan University, 220 Handan Road, Shanghai 200433, People's Republic of China, Fax: (+86)-216-510-2412

  2. 2

    State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai 200032, People's Republic of China

Publication History

  1. Issue published online: 18 SEP 2007
  2. Article first published online: 6 SEP 2007
  3. Manuscript Revised: 1 JUL 2007
  4. Manuscript Received: 20 FEB 2007

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Keywords:

  • arenes;
  • aziridines;
  • gold(III) chloride;
  • ring-opening reaction;
  • silver triflate

Abstract

Gold(III) chloride/silver triflate was found to a highly efficient catalyst in the ring-opening of aziridines with electron-rich arenes and the desired β-arylamines were afforded in good to excellent yields under mild reaction conditions.

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