Synthesis 2014; 46(20): 2727-2733
DOI: 10.1055/s-0034-1379208
practical synthetic procedures
© Georg Thieme Verlag Stuttgart · New York

Pd(II)/Bu4NBr/DMSO Catalytic System for Practical Synthesis of Indoles and Pyrroles from Imines through Aerobic Dehydrogenative Cyclization

Wei Wen Tan
Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore   Fax: +6569711961   Email: nyoshikai@ntu.edu.sg
,
Xiaoya Hou
Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore   Fax: +6569711961   Email: nyoshikai@ntu.edu.sg
,
Naohiko Yoshikai*
Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore   Fax: +6569711961   Email: nyoshikai@ntu.edu.sg
› Author Affiliations
Further Information

Publication History

Received: 17 May 2014

Accepted after revision: 03 September 2014

Publication Date:
25 September 2014 (online)


Abstract

N-Aryl- and N-allylimines derived typically from substituted acetophenones undergo palladium(II)-catalyzed dehydrogenative cyclization reactions in the presence of tetrabutylammonium bromide and molecular oxygen in DMSO to afford indole and pyrrole derivatives, respectively, in moderate to good yields. The reactions are operationally simple and can be readily performed on multigram scales (up to 55 mmol).

Supporting Information

 
  • References

    • 1a d’Ischia M, Napolitano A, Pezzella A In Comprehensive Heterocyclic Chemistry III . Vol. 3. Katritzky AR, Ramsden CA, Scriven EF. V, Taylor RJ. K. Elsevier; Oxford: 2008: 353-388
    • 1b Fan H, Peng J, Hamann MT, Hu JF. Chem. Rev. 2008; 108: 264
    • 1c Kochanowska-Karamyan AJ, Hamann MT. Chem. Rev. 2010; 110: 4489
    • 1d Sundberg RJ. Indoles . Academic Press; San Diego: 1996
    • 2a Gribble GW. J. Chem. Soc., Perkin Trans. 1 2000; 1045
    • 2b Humphrey GR, Kuethe JT. Chem. Rev. 2006; 106: 2875
    • 2c Zeni G, Larock RC. Chem. Rev. 2006; 106: 4644
    • 2d Cacchi S, Fabrizi G. Chem. Rev. 2011; 111: PR215
    • 2e Platon M, Amardeil R, Djakovitch L, Hierso JC. Chem. Soc. Rev. 2012; 41: 3929
    • 2f Inman M, Moody CJ. Chem. Sci. 2013; 4: 29
  • 3 Yoshikai N, Wei Y. Asian J. Org. Chem. 2013; 2: 466 , and references cited therein

    • For recent examples of indole synthesis via C–H activation not cited in ref. 3, see:
    • 4a Wang C, Sun H, Fang Y, Huang Y. Angew. Chem. Int. Ed. 2013; 52: 5795
    • 4b Zhao D, Shi Z, Glorius F. Angew. Chem. Int. Ed. 2013; 52: 12426
    • 4c Liu B, Song C, Sun C, Zhou S, Zhu J. J. Am. Chem. Soc. 2013; 135: 16625
    • 4d Cajaraville A, López S, Varela JA, Saá C. Org. Lett. 2013; 15: 4576
    • 4e Wang C, Huang Y. Org. Lett. 2013; 15: 5294
    • 4f Ren L, Shi Z, Jiao N. Tetrahedron 2013; 69: 4408
    • 4g Piou T, Neuville L, Zhu J. Tetrahedron 2013; 69: 4415

      For recent examples of pyrrole synthesis via C–H activation not cited in ref. 3, see:
    • 5a Lian Y, Huber T, Hesp KD, Bergman RG, Ellman JA. Angew. Chem. Int. Ed. 2013; 52: 629
    • 5b Du J, Zhou B, Yang Y, Li Y. Chem. Asian J. 2013; 8: 1386
    • 5c Zhao M.-N, Ren Z.-H, Wang Y.-Y, Guan Z.-H. Org. Lett. 2014; 16: 608
    • 6a Åkermark B, Eberson L, Jonsson E, Pettersson E. J. Org. Chem. 1975; 40: 1365
    • 6b Knölker H.-J. Chem. Lett. 2009; 38: 8 ; and references cited therein
    • 7a Würtz S, Rakshit S, Neumann JJ, Dröge T, Glorius F. Angew. Chem. Int. Ed. 2008; 47: 7230
    • 7b Neumann JJ, Rakshit S, Dröge T, Würtz S, Glorius F. Chem. Eur. J. 2011; 17: 7298
  • 8 Wei Y, Deb I, Yoshikai N. J. Am. Chem. Soc. 2012; 134: 9098
  • 9 Shi Z, Glorius F. Angew. Chem. Int. Ed. 2012; 51: 9220

    • A similar Pd(II)-based aerobic catalytic system has been used for oxidative cyclization of o-alkynylanilines to indoles:
    • 10a Yao B, Wang Q, Zhu J. Angew. Chem. Int. Ed. 2012; 51: 5170
    • 10b Yao B, Wang Q, Zhu J. Angew. Chem. Int. Ed. 2012; 51: 12311
  • 11 Chen Z, Lu B, Ding Z, Gao K, Yoshikai N. Org. Lett. 2013; 15: 1966
    • 12a Shi Z, Suri M, Glorius F. Angew. Chem. Int. Ed. 2013; 52: 4892
    • 12b Meng L, Wu K, Liu C, Lei A. Chem. Commun. 2013; 49: 5853

      For reviews on palladium oxidase catalysis, see:
    • 13a Stahl SS. Angew. Chem. Int. Ed. 2004; 43: 3400
    • 13b Campbell AN, Stahl SS. Acc. Chem. Res. 2012; 45: 851
    • 13c Wu W, Jiang H. Acc. Chem. Res. 2012; 45: 1736
  • 14 Hajra A, Wei Y, Yoshikai N. Org. Lett. 2012; 15: 5488
  • 15 Girard SA, Hu X, Knauber T, Zhou F, Simon M.-O, Deng G.-J, Li C.-J. Org. Lett. 2012; 14: 5606