Synlett 2016; 27(16): 2301-2313
DOI: 10.1055/s-0035-1561470
account
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Spirocyclic and Fused Cyclic Compounds by Transition-Metal-Catalyzed Intramolecular Friedel–Crafts-Type Reactions of Phenol Derivatives

Tetsuhiro Nemoto*
a   Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1, Inohana, Chuo-ku, Chiba 260-8675, Japan
b   Molecular Chirality Research Center, Chiba University, 1-33, Yayoi-cho, Inage-ku, Chiba 263-8522, Japan   Email: tnemoto@faculty.chiba-u.jp
,
Yasumasa Hamada
a   Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1, Inohana, Chuo-ku, Chiba 260-8675, Japan
› Author Affiliations
Further Information

Publication History

Received: 13 April 2016

Accepted after revision: 09 May 2016

Publication Date:
25 July 2016 (online)


Abstract

This account describes the development of novel dearomatization reactions of phenols using transition-metal-catalyzed ipso-Friedel–Crafts-type processes. In general, phenols function as O-nucleo­philes in transition-metal-catalyzed allylic substitution reactions, providing the corresponding aryl ethers. We found that, however, an intramolecular ipso-Friedel–Crafts allylic alkylation of phenols proceeded smoothly in the presence of a palladium catalyst, producing various spiro[4.5]cyclohexadienone derivatives. This finding led us to launch detailed investigations into this type of reaction. Pd-catalyzed intramolecular Friedel–Crafts allylic alkylation of phenols was next examined to synthesize 10-vinyl 9,10-dihydrophenanthrene derivatives. This reaction was successfully extended to a catalytic asymmetric process. We also developed a novel synthetic method for spiro[5.5]cyclohexadienones based on a Pd-catalyzed intramolecular ipso-Friedel–Crafts-type addition of phenols to η3-propargylpalladium(II) intermediates. Mechanistic studies revealed that the present reaction proceeds through a rearomatization-assisted oxidative addition. Moreover, a Au-catalyzed intramolecular ipso-Friedel–Crafts alkenylation of phenols with a terminal alkyne is discussed.

1 Introduction

2 Pd-Catalyzed Intramolecular Friedel–Crafts Allylic Alkylation of Phenols

2.1 Synthesis of Spirocyclohexadienone Derivatives by Pd-Catalyzed Intramolecular ipso-Friedel–Crafts Allylic Alkylation of Phenols

2.2 Mechanistic Considerations

2.3 Application to Cascade Reaction Processes

2.4 Asymmetric Synthesis of Dihydrophenanthrene Derivatives by Pd-Catalyzed Asymmetric Intramolecular Friedel–Crafts Allylic Alkylation of Phenols

3 Dearomatization of Phenols by Activation of Propargyl Carbonates with a Pd Catalyst

4 Au-Catalyzed Intramolecular ipso-Friedel–Crafts Alkenylation of Phenols

5 Summary and Outlook

 
  • References


    • For reviews, see:
    • 1a Roche ST, Porco Jr JA. Angew. Chem. Int. Ed. 2011; 50: 4068
    • 1b Zhuo C.-X, Zhang W, You S.-L. Angew. Chem. Int. Ed. 2012; 51: 12662
    • 2a Tamura Y, Yakura T, Haruta J, Kita Y. J. Org. Chem. 1987; 52: 3927
    • 2b Dohi T, Maruyama A, Yoshimura M, Morimoto K, Tohma H, Kita Y. Angew. Chem. Int. Ed. 2005; 44: 6193
    • 2c Dohi T, Maruyama A, Minamitsuji Y, Takenaga N, Kita Y. Chem. Commun. 2007; 1224
    • 2d Dohi T, Minamitsuji Y, Maruyama A, Hirose S, Kita Y. Org. Lett. 2008; 10: 3559
    • 2e Dohi T, Maruyama A, Takenaga N, Senami K, Minamitsuji Y, Fujioka H, Caemmerer SB, Kita Y. Angew. Chem. Int. Ed. 2008; 47: 3787
    • 2f Uyanik M, Yasui T, Ishihara K. Angew. Chem. Int. Ed. 2010; 49: 2175

      For selected examples, see: Metal-mediated methods
    • 3a Pigge FC, Coniglio JJ, Dalvi R. J. Am. Chem. Soc. 2006; 128: 3498
    • 3b Chiba S, Zhang L, Lee J.-Y. J. Am. Chem. Soc. 2010; 132: 7266
    • 3c Matsuura BS, Condie AG, Buff RC, Karahalis GJ, Stephenson CR. J. Org. Lett. 2011; 13: 6320
    • 3d Rousseaux S, García-Fortanet J, Del Aguila Sanchez MA, Buchwald SL. J. Am. Chem. Soc. 2011; 133: 9282
    • 3e Xiao Q, Jackson JJ, Basak A, Bowler JM, Miller BG, Zakarian A. Nat. Chem. 2013; 5: 410
    • 3f Li Y, Zhang L, Zhang L, Wu Y, Gong Y. Eur. J. Org. Chem. 2013; 8039
    • 3g Xu R.-Q, Gu Q, Wu W.-T, Zhao Z.-A, You S.-L. J. Am. Chem. Soc. 2014; 136: 15469
    • 3h Zheng J, Wang S.-B, Zheng C, You S.-L. J. Am. Chem. Soc. 2015; 137: 4880
    • 3i Luo L, Zheng H, Liu J, Wang H, Wang Y, Luan X. Org. Lett. 2016; 18: 2082
    • 3j Yuan Z, Wei W, Lin A, Yao H. Org. Lett. 2016; 18: 3307

    • Radical cyclization:
    • 3k González-López de Turiso F, Curran DP. Org. Lett. 2005; 7: 151
    • 3l Lanza T, Leardini R, Minozzi M, Nanni D, Spagnolo P, Zanardi G. Angew. Chem. Int. Ed. 2008; 47: 9439
    • 3m Zhang H, Gu Z, Xu P, Hu H, Cheng Y, Zhu C. Chem. Commun. 2016; 52: 477

    • Halocyclization
    • 3n Zhang X, Larock RC. J. Am. Chem. Soc. 2005; 127: 12230
    • 3o Tang B.-X, Tang D.-J, Tang S, Yu Q.-F, Zhang Y.-H, Liang Y, Zhong P, Li J.-H. Org. Lett. 2008; 10: 1063
    • 3p Yin Q, You S.-L. Org. Lett. 2012; 14: 3526
    • 4a Winstein S, Baird R. J. Am. Chem. Soc. 1957; 79: 756
    • 4b Masamune S. J. Am. Chem. Soc. 1961; 83: 1009
    • 4c Baird R, Winstein S. J. Am. Chem. Soc. 1962; 84: 788
    • 5a Lalic G, Corey EJ. Org. Lett. 2007; 9: 4921
    • 5b Dai M, Danishefsky SJ. Tetrahedron Lett. 2008; 49: 6610
    • 5c Magnus P, Sane N, Fauber BP, Lynch V. J. Am. Chem. Soc. 2009; 131: 16045
    • 5d Eey ST.-C, Lear MJ. Org. Lett. 2010; 12: 5510
  • 6 For a preceding personal account, see: Nemoto T, Hamada Y. J. Synth. Org. Chem., Jpn. 2015; 73: 977

    • For reviews on transition-metal-catalyzed allylic substitution reactions, see:
    • 7a Trost BM, Crawley ML. Chem. Rev. 2003; 103: 2921
    • 7b Lu Z, Ma S. Angew. Chem. Int. Ed. 2008; 47: 258
  • 8 Nemoto T, Ishige Y, Yoshida M, Kohno Y, Kanematsu M, Hamada Y. Org. Lett. 2010; 12: 5020
  • 9 Yoshida M, Nemoto T, Zhao Z, Ishige Y, Hamada Y. Tetrahedron: Asymmetry 2012; 23: 859
  • 10 Wu Q.-F, Liu W.-B, Zhuo C.-X, Rong Z.-Q, Ye K.-Y, You S.-L. Angew. Chem. Int. Ed. 2011; 50: 4455
    • 11a Zhuo C.-X, You S.-L. Angew. Chem. Int. Ed. 2013; 52: 10056
    • 11b Zhuo C.-X, You S.-L. Adv. Synth. Catal. 2014; 356: 2020
  • 12 For a review see: Tsuji J. Palladium Reagents and Catalysts: New Perspectives for the 21st Century . John Wiley & Sons, Ltd; Chichester: 2004. Chap. 3.2.9.2
  • 13 Nemoto T, Nozaki T, Yoshida M, Hamada Y. Adv. Synth. Catal. 2013; 355: 2693
  • 14 Yoshida M, Nozaki T, Nemoto T, Hamada Y. Tetrahedron 2013; 69: 9609
  • 15 Suzuki Y, Nemoto T, Kakugawa K, Hamajima A, Hamada Y. Org. Lett. 2012; 14: 2350
  • 16 Suzuki Y, Matsuo N, Nemoto T, Hamada Y. Tetrahedron 2013; 69: 5913
  • 17 For an example of Ir-catalyzed asymmetric intramolecular Friedel–Crafts allylic alkylation of phenols, see: Xu Q.-L, Dai L.-X, You S.-L. Org. Lett. 2012; 14: 2579
  • 18 Tsutsumi K, Ogoshi S, Nishiguchi S, Kurosawa H. J. Am. Chem. Soc. 1998; 120: 1938

    • For reviews, see:
    • 19a Tsuji J. Palladium Reagents and Catalysts: New Perspectives for the 21st Century . John Wiley & Sons, Ltd; Chichester: 2004. Chap. 6
    • 19b Guo L.-N, Duan X.-H, Liang Y.-M. Acc. Chem. Res. 2011; 44: 111
  • 20 Nemoto T, Zhao Z, Yokosaka T, Suzuki Y, Wu R, Hamada Y. Angew. Chem. Int. Ed. 2013; 52: 2217
  • 21 Nemoto T, Wu R, Zhao Z, Yokosaka T, Hamada Y. Tetrahedron 2013; 69: 3403

    • For reviews, see:
    • 22a Bandini M. Chem. Soc. Rev. 2011; 47: 1358
    • 22b de Mendoza P, Echavarren AM. Pure. Appl. Chem. 2010; 82: 801
  • 23 Nemoto T, Matsuo N, Hamada Y. Adv. Synth. Catal. 2014; 356: 2417
  • 24 For an example of Au-catalyzed intramolecular dearomatization of naphthols through an alkyne carbocyclization process, see: Wu W.-T, Xu R.-Q, Zhang L, You S.-L. Chem. Sci. 2016; 7: 3427