Synthesis 2011(1): 23-29  
DOI: 10.1055/s-0030-1258348
PSP
© Georg Thieme Verlag Stuttgart ˙ New York

Efficient Preparation of Polyfunctional Indoles via a Zinc Organometallic Variation of the Fischer Indole Synthesis

Zhi-Guang Zhanga,b, Benjamin A. Haaga, Jin-Shan Lib, Paul Knochel*a
a Department Chemie, Ludwig-Maximilians-Universität München, Butenandtstr. 5-13, Haus F, 81377 Munich, Germany
Fax: +49(89)218077680; e-Mail: paul.knochel@cup.uni-muenchen.de;
b State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, P. R. of China
Further Information

Publication History

Received 28 October 2010
Publication Date:
03 December 2010 (online)

Abstract

Functionalized organozinc reagents readily react with various aryldiazonium salts furnishing regioselectively polyfunctional indoles after heating with microwave irradiation. This new organometallic variation of the Fischer indole synthesis tolerates a wide range of functional groups and can be readily scaled up.

    References

  • 1a Sundberg RT. Indoles   Academic Press; London: 1996. 
  • 1b Comprehensive Heterocyclic Chemistry II   Vol. 2:  Katritzky AR. Rees CW. Scriven EFV. Pergamon Press; Oxford: 1996.  p.207-257  
  • 1c Sundberg RJ. In Comprehensive Heterocyclic Chemistry II   Vol. 2:  Katritzky AR. Ress CW. Scriven EFV. Bird CW. Pergamon Press; Oxford: 1996. 
  • 1d Joule A. In Science of Synthesis   Vol. 10:  Thomas EJ. Thieme; Stuttgart: 2000.  Chap. 10.13.
  • 2a Humphrey GR. Kuethe JT. Chem. Rev.  2006,  106:  2875 
  • 2b Zeni G. Larock RC. Chem. Rev.  2004,  104:  2285 
  • 3 Cacchi S. Fabrizi G. Chem. Rev.  2005,  105:  2873 
  • 4a Fischer E. Jourdan F. Ber. Dtsch. Chem. Ges.  1883,  16:  2241 
  • 4b Robinson B. The Fischer Indole Synthesis   Wiley-Interscience; New York: 1982. 
  • 5 Handbook of Functionalized Organometallics   Knochel P. Wiley-VCH; Weinheim: 2005. 
  • 6 Haag BA. Zhang Z.-G. Li J.-S. Knochel P. Angew. Chem. Int. Ed.  2010,  49: in press; DOI: anie.201005319
  • 7 Erdik E. Organozinc Reagents in Organic Synthesis   CRC-Press; Boca Raton: 1996. 
  • 8a Dong Z. Manolikakes G. Li J. Knochel P. Synthesis  2009,  681 
  • 8b Despotopoulou C. Gignoux C. McConnell D. Knochel P. Synthesis  2009,  3661 
  • 8c Monzon G. Knochel P. Synlett  2010,  304 
  • 8d Metzger A. Argyo C. Knochel P. Synthesis  2010,  882 
  • 9 Krasovskiy A. Malakhov V. Gavryushin A. Knochel P. Angew. Chem. Int. Ed.  2006,  45:  6040 
  • 10a Piller FM. Appukkuttan P. Gavryushin A. Helm M. Knochel P. Angew. Chem. Int. Ed.  2008,  47:  6802 
  • 10b Piller FM. Metzger A. Schade MA. Haag BA. Gavryushin A. Knochel P. Chem. Eur. J.  2009,  15:  7192 
  • 11a Haag BA. Peng Z. Knochel P. Org. Lett.  2009,  11:  4270 
  • 11b Sapountzis I. Knochel P. Angew. Chem. Int. Ed.  2004,  43:  897 
  • 12a Rice LM. Hertz E. Freed ME. J. Med. Chem.  1964,  7:  313 
  • 12b Baxter BL. Gluckman MI. Nature  1969,  223:  750 
  • 13 Chen J. Hu Y. Synth. Commun.  2006,  36:  1485