Synlett 2012; 23(19): 2723-2728
DOI: 10.1055/s-0032-1317169
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© Georg Thieme Verlag Stuttgart · New York

Acid-Catalyzed Ring-Opening Isomerizations of Cyclopropenes

Lien H. Phun
School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA 30332, USA   Fax: +1(404)8947452   Email: stefan.france@chemistry.gatech.edu
,
Joel Aponte-Guzman
School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA 30332, USA   Fax: +1(404)8947452   Email: stefan.france@chemistry.gatech.edu
,
Stefan France*
School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA 30332, USA   Fax: +1(404)8947452   Email: stefan.france@chemistry.gatech.edu
› Author Affiliations
Further Information

Publication History

Received: 09 July 2012

Accepted after revision: 06 August 2012

Publication Date:
31 October 2012 (online)


Abstract

Acid-catalyzed cyclopropene cycloisomerizations are discussed as a means to generate ring systems. Herein, the recent results obtained in our group are contrasted with previous examples in the literature. Particular emphasis is placed on the mode of activation which, for our case, results in a different ring-opening mechanism than previously observed. The potential of the method as a tool for organic chemists is demonstrated by the synthesis of a host of benzo-fused heteroaromatic and heterobiaryl products.

 
  • References and Notes

  • 1 Randic M, Borcic S. J. Chem. Soc. A 1967; 586
  • 2 For cyclopropenes, the term ‘cycloisomerization’ refers to a structural reorganization resulting in the formation of a new ring that occurs upon ring opening.
    • 3a Rubin M, Rubina M, Gevorgyan V. Chem. Rev. 2007; 107: 3117
    • 3b Miege F, Meyer C, Cossy J. Beilstein J. Org. Chem. 2011; 7: 717
  • 4 Zhu Z.-B, Wei Y, Shi M. Chem. Soc. Rev. 2011; 40: 5534
  • 5 Chuprakov S, Gevorgyan V. Org. Lett. 2007; 9: 4463
    • 6a Rinehart KL. Jr, Goldberg SI, Tarimu CL, Culbertson TP. J. Am. Chem. Soc. 1961; 83: 225
    • 6b Kircher HW. J. Org. Chem. 1964; 29: 1979
  • 7 Breslow R. Rearrangements in Small Ring Compounds . In Molecular Rearrangements . de Mayo P. Interscience Publishers; New York: 1963: 233-294
  • 8 Kudryavtseva GA, Nesmeyanova OA. Izv. Akad. Nauk SSSR, Ser. Khim. 1974; 2357
  • 9 Padwa A, Wannamaker MW, Dyszlewski AD. J. Org. Chem. 1987; 52: 4760
  • 10 Shao L.-X, Zhang Y.-P, Qi M.-H, Shi M. Org. Lett. 2007; 9: 117
  • 11 Kotha S, Misra S, Halder S. Tetrahedron 2008; 64: 10775
  • 12 Zhu Z.-B, Shi M. J. Org. Chem. 2009; 74: 2481
    • 13a Zhu Z.-B, Shi M. Chem.–Eur. J. 2008; 14: 10219
    • 13b Zhu Z.-B, Wei Y, Shi M. Chem.–Eur. J. 2009; 15: 7543 ; the regioisomeric indene formed is shown in Figure 2

      For representative reviews see:
    • 14a Mel'nikov MY, Budynina EM, Ivanova OA, Trushkov IV. Mendeleev Commun. 2011; 21: 293
    • 14b Lebold TP, Kerr MA. Pure Appl. Chem. 2010; 82: 1797
    • 14c Yu M, Pagenkopf BL. Tetrahedron 2005; 61: 321
    • 14d Reissig HU, Zimmer R. Chem. Rev. 2003; 103: 1151
    • 15a Patil DV, Phun LH, France S. Org. Lett. 2010; 12: 5684
    • 15b Phun LH, Patil DV, Cavitt MA, France S. Org. Lett. 2011; 13: 1952
    • 15c Patil DV, Cavitt MA, Grzybowski P, France S. Chem. Commun. 2011; 47: 10278
    • 15d Patil DV, Cavitt MA, France S. Heterocycles 2012; 84: 1363

      For recent examples see:
    • 16a Liu Y, Ma S. Chem. Sci. 2011; 2: 811
    • 16b Chen J, Ma S. J. Org. Chem. 2009; 74: 5595
    • 16c Wang Y, Lam HW. J. Org. Chem. 2009; 74: 1353
    • 16d Yang Y, Fordyce EA. F, Chen FY, Lam HW. Angew. Chem. Int. Ed. 2008; 47: 7350
  • 17 Phun LH, Aponte-Guzman J, France S. Angew. Chem. Int. Ed. 2012; 51: 3198
  • 18 González-Bobes F, Fenster MD. B, Kiau S, Kolla L, Kolotuchin S, Soumeillant M. Adv. Synth. Catal. 2008; 350: 813
  • 19 Briones JF, Davies HM. Tetrahedron 2011; 67: 4313
  • 20 The cyclopropenation reaction is under kinetic control. The cyclopropene represents the kinetic product while the furan represents the thermodynamic product. Depending on the substrate and which Rh(II) catalyst is used the ratio of the two products varies. This represents an update from the original publication.
  • 21 When α-diazo-1,3-diketones were used with alkynes under the standard cyclopropenation conditions, cyclopropenes were observed, as only benzo-fused products were obtained. We suspect the formation of a more reactive rhodium carbenoid.
  • 22 van Alem K, Lodder G, Zuilhof H. J. Phys. Chem. A 2002; 106: 10681