Citation: Rong Fan, Chen Tan, Yongguo Liu, Yun Wei, Xiaowen Zhao, Xinyuan Liu, Jiajing Tan, Hiroto Yoshida. A leap forward in sulfonium salt and sulfur ylide chemistry[J]. Chinese Chemical Letters, ;2021, 32(1): 299-312. doi: 10.1016/j.cclet.2020.06.003 shu

A leap forward in sulfonium salt and sulfur ylide chemistry


  • Author Bio:





    Jiajing Tan obtained his BS from University of Science and Technology of China in 2008. He received his PhD in 2013 under the supervision of Professor Hisashi Yamamoto at the University of Chicago. From 2013–2015, he worked at Merck & Co. Then, he started his academic career at Beijing University of Chemical and Technology. His current research interests are aryne chemistry and green chemistry.

  • * Corresponding authors.
    E-mail addresses: weiyun@mail.buct.edu.cn (Y. Wei), tanjj@mail.buct.edu.cn (J. Tan), yhiroto@hiroshima-u.ac.jp (H. Yoshida).
  • Received Date: 24 April 2020
    Revised Date: 21 May 2020
    Accepted Date: 1 June 2020
    Available Online: 3 June 2020

Figures(36)

  • Sulfonium salts and sulfur ylides are important S(Ⅳ) motifs, and have displayed many unique reactivities to provide simple, effective, and often stereoselective synthesis toward sulfur containing compounds. Impressive developments have been witnessed within this field during the past several years. In light of the increasing demand of organosulfur compounds across the range of chemical sciences, our aim of this review is to provide a concise overview of recent advances of sulfonium salt and sulfur ylide chemistry. Selected examples are organized in three parts on the basis of their role in organic reactions (reactants, intermediates and catalysts).
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    1. [1]

      (a) R.J. Cremlyn, An Introduction to Organosulfur Chemistry, John Wiley & Sons, Hoboken, 1996;
      (b) P.C.B. Page, Organosulfur Chemistry I., Springer, Heidelberg, 1999;
      (c) C.M. Rayner, Advances in Sulfur Chemistry, JAI Press, Greenwich, 2000;
      (d) A.Q. Acton, Sulfur Compounds: Advances in Research and Application, Scholarly Editions, Atlanta, 2012.

    2. [2]

      (a) E.A. Ilardi, E. Vitaku, J.T. Njardarson, J. Med. Chem. 57(2014) 2832-2842;
      (b) B.R. Smith, C.M. Eastman, J.T. Njardarson, J. Med. Chem. 57(2014) 9764-9773.

    3. [3]

      (a) K.L. Dunbar, D.H. Scharf, A. Litomska, C. Hertweck, Chem. Rev. 117(2017) 5521-5577;
      (b) M.H. Feng, B.Q. Tang, S. Liang, X.F. Jiang, Curr. Top. Med. Chem. 16(2016) 1200-1216.

    4. [4]

      (a) L.D. Wang, W. He, Z.K. Yu, Chem. Soc. Rev. 42(2013) 599-621;
      (b) S.G. Modha, V.P. Mehta, E.V. Van der Eycken, Chem. Soc. Rev. 42(2013) 5042-5055;
      (c) D. Kaiser, I. Klose, R. Oost, et al., Chem. Rev. 119(2019) 8701-8780.

    5. [5]

      (a) A.W. Johnson, R.B. Lacount, J. Am. Chem. Soc. 83(1961) 417-423;
      (b) E.J. Corey, M. Chaykovsky, J. Am. Chem. Soc. 84(1962) 867-868;
      (c) S.Q. Guo, N.N. Zhang, X.Z. Tang, et al., Chin. Chem. Lett. 30(2019) 406-408.

    6. [6]

      L. Kurti, B. Czako, Strategic Applications of Named Reactions in Organic Synthesis, Elsevier, Burlington, 2005, pp. 294-295.

    7. [7]

      (a) R. Oost, R.J.D. Neuhaus, J. Merad, N. Maulide, Sulfur Ylides in Organic Synthesis and Transition Metal Catalysis, Structure and Bonding, Springer, Berlin, Heidelberg, 2017;
      (b) J.D. Neuhaus, R. Oost, J. Merad, N. Maulide, Top. Curr. Chem. 376(2018) 15;
      (c) L.Q. Lu, T.R. Li, Q. Wang, W.J. Xiao, Chem. Soc. Rev. 46(2017) 4135-4149;
      (d) M. Mondal, S. Chen, N.J. Kerrigan, Molecules 23(2018) 738-767;
      (e) F. Pan, Z.J. Shi, ACS Catal. 4(2014) 280-288;
      (f) K. Gao, S. Otsuka, A. Baralle, et al., J. Synth. Org. Chem. Jpn. 74(2016) 1119-1127;
      (g) D.H. Ortgies, A. Hassanpour, F. Chen, et al., Eur. J. Org. Chem. 2016(2016) 408-425;
      (h) S. Otsuka, K. Nogi, H. Yorimitsu, Top. Curr. Chem. 376(2018) 13;
      (i) P. Chauhan, S. Mahajan, D. Enders, Chem. Rev. 114(2014) 8807-8864.

    8. [8]

      (a) T.J. Colacot, New Trends in Cross-Coupling: Theory and Applications, 4th. ed., Royal Society of Chemistry, British, 2014;
      (b) Á. Molnár, Palladium-Catalyzed Coupling Reactions: Practical Aspects and Future Developments, Wiley-VCH, Weinheim, Germany, 2013;
      (c) M.L. Crawley, B.M. Trost, Applications of Transition Metal Catalysis in Drug Discovery and Development, Wiley, New York, 2012;
      (d) J.J. Tan, Y.G. Chen, H.M. Li, N. Yasuda, J. Org. Chem. 79(2014) 8871-8876.

    9. [9]

      J. Srogl, G.D. Allred, L.S. Liebeskind, J. Am. Chem. Soc. 119(1997) 12376-12377.  doi: 10.1021/ja9726926

    10. [10]

      (a) Z.Y. Tian, Y.T. Hu, H.B. Teng, C.P. Zhang, Tetrahedron 59(2018) 299-309;
      (b) S.M. Wang, H.X. Song, X.Y. Wang, et al., Chem. Commun. (Camb. ) 52(2016) 11893-11896;
      (c) S.M. Wang, X.Y. Wang, H.L. Qin, C.P. Zhang, Chem. Eur. J. 22(2016) 6542-6546;
      (d) Z.Y. Tian, S.M. Wang, S.J. Jia, et al., Org. Lett. 19(2017) 5454-5457;
      (e) Z.Y. Tian, C.P. Zhang, Chem. Commun. (Camb. ) 55(2019) 11936-11939;
      (f) X.Y. Wang, H.X. Song, S.M. Wang, et al., Tetrahedron 72(2016) 7606-7612.

    11. [11]

      (a) D. Uno, H. Minami, S. Otsuka, et al., Chem. Asian J. 13(2018) 2397-2400;
      (b) H. Minami, K. Nogi, H. Yorimitsu, Org. Lett. 21(2019) 2518-2522;
      (c) H. Minami, S. Otsuka, K. Nogi, H. Yorimitsu, ACS Catal. 8(2018) 579-583.

    12. [12]

      D.C. Simkó, P. Elekes, V. Pázmándi, Z. Novák, Org. Lett. 20(2018) 676-679.  doi: 10.1021/acs.orglett.7b03813

    13. [13]

      P. Cowper, Y. Jin, M.D. Turton, et al., Angew. Chem. Int. Ed. 55(2016) 2564-2568.  doi: 10.1002/anie.201510666

    14. [14]

      M.H. Aukland, F.J.T. Talbot, J.A. Fernández-Salas, et al., Angew. Chem. Int. Ed. 57(2018) 9785-9789.  doi: 10.1002/anie.201805396

    15. [15]

      (a) D. Ravelli, S. Protti, M. Fagnoni, Chem. Rev. 116(2016) 9850-9913;
      (b) Q.Q. Zhou, Y.Q. Zou, L.Q. Lu, W.J. Xiao, Angew. Chem. Int. Ed. 58(2019) 1586-1604;
      (c) N.A. Romero, D.A. Nicewicz, Chem. Rev. 116(2016) 10075-10166.

    16. [16]

      I. Ghosh, L. Marzo, A. Das, et al., Acc. Chem. Res. 49(2016) 1566-1577.  doi: 10.1021/acs.accounts.6b00229

    17. [17]

      S. Donck, A. Baroudi, L. Fensterbank, et al., Adv. Synth. Catal. 355(2013) 1477-1482.  doi: 10.1002/adsc.201300040

    18. [18]

      S. Otsuka, K. Nogi, T. Rovis, H. Yorimitsu, Chem. Asian J. 14(2019) 532-536.  doi: 10.1002/asia.201801732

    19. [19]

      (a) F. Berger, M.B. Plutschack, J. Riegger, et al., Nature 567(2019) 223-228;
      (b) J.K. Li, J.T. Chen, R.C. Sang, et al., Nat. Chem. 12(2020) 56-62;
      (c) P.S. Engl, A.P. Häring, F. Berger, et al., J. Am. Chem. Soc. 141(2019) 13346-13351;
      (d) F. Ye, F. Berger, H. Jia, et al., Angew. Chem. Int. Ed. 58(2019) 14615-14619;
      (e) R.C. Sang, S.E. Korkis, W.Q. Su, et al., Angew. Chem. Int. Ed. 58(2019) 16161-16166.

    20. [20]

      C. Huang, J. Feng, R. Ma, et al., Org. Lett. 21(2019) 9688-9692.  doi: 10.1021/acs.orglett.9b03850

    21. [21]

      S. Rohrbach, A.J. Smith, J.H. Pang, et al., Angew. Chem. Int. Ed. 58(2019) 16368-16388.  doi: 10.1002/anie.201902216

    22. [22]

      (a) V. Bernard-Gauthier, T.L. Collier, S.H. Liang, N. Vasdev, Drug Discov. Today Technol. 25(2017) 19-26;
      (b) G. Pascali, L. Matesic, B. Zhang, et al., EJNMMI Radiopharm. Chem. 2(2017) 9-26.

    23. [23]

      (a) L.J. Mu, C.R. Fischer, J.P. Holland, et al., Eur. J. Org. Chem. 2012(2012) 889-892;
      (b) K. Sander, T. Gendron, E. Yiannaki, et al., Sci. Rep. 5(2015) 9941-9945.

    24. [24]

      T. Gendron, K. Sander, K. Cybulska, et al., J. Am. Chem. Soc. 140(2018) 11125-11132.  doi: 10.1021/jacs.8b06730

    25. [25]

      P. Xu, D. Zhao, F. Berger, et al., Angew. Chem. Int. Ed. 59(2020) 1956-1960.  doi: 10.1002/anie.201912567

    26. [26]

      (a) X.X. Ming, Z.Y. Tian, C.P. Zhang, Chem. Asian J. 14(2019) 3370-3379;
      (b) Z.Y. Tian, X.X. Ming, H.B. Teng, et al., Chem. Eur. J. 24(2018) 13744-13748.

    27. [27]

      J.N. Zhao, M. Kayumov, D.Y. Wang, A. Zhang, Org. Lett. 21(2019) 7303-7306.  doi: 10.1021/acs.orglett.9b02584

    28. [28]

      (a) Y.F. Liu, X.X. Shao, P.P. Zhang, et al., Org. Lett. 17(2015) 2752-2755;
      (b) J.S. Zhu, Y.F. Liu, Q.L. Shen, Angew. Chem. Int. Ed. 55(2016) 9050-9054;
      (c) Y.F. Liu, L. Lu, Q.L. Shen, Angew. Chem. Int. Ed. 56(2017) 9930-9934.

    29. [29]

      (a) C.F. Ni, M.Y. Hu, J.B. Hu, Chem. Rev. 115(2015) 765-825;
      (b) C. Zhang, Org. Biomol. Chem. 12(2014) 6580-6589;
      (c) S. Barata-Vallejo, B. Lantaño, A. Postigo, Chem. Eur. J. 20(2014) 16806-16829;
      (d) G.K. Liu, X. Li, W.B. Qin, et al., Chin. Chem. Lett. 30(2019) 1515-1518.

    30. [30]

      S. Verhoog, C.W. Kee, Y.L. Wang, et al., J. Am. Chem. Soc. 140(2018) 1572-1575.  doi: 10.1021/jacs.7b10227

    31. [31]

      (a) B. Waldecker, F. Kraft, C. Golz, M. Alcarazo, Angew. Chem. Int. Ed. 57(2018) 12538-12542;
      (b) X.D. Li, C. Golz, M. Alcarazo, Angew. Chem. Int. Ed. 58(2019) 9496-9500.

    32. [32]

      (a) Y. Xia, D. Qiu, J.B. Wang, Chem. Rev. 117(2017) 13810-13889;
      (b) M.P. Doyle, R. Duffy, M. Ratnikov, L. Zhou, Chem. Rev. 110(2010) 704-724;
      (c) Q.Q. Cheng, M.P. Doyle, Adv. Organomet. Chem. 66(2016) 1-31;
      (d) Z.F. Liu, X.F. Yue, Q. Wei, K.L. Han, Chin. Chem. Lett. 18(2007) 107-110.

    33. [33]

      (a) Z. Sheng, Z.K. Zhang, C.H. Chu, et al., Tetrahedron 73(2017) 4011-4022;
      (b) X.Y. Wang, X. Wang, J.B. Wang, Tetrahedron 75(2019) 949-964;
      (c) Z.K. Zhang, Z. Sheng, W.Z. Yu, et al., Nat. Chem. 9(2017) 970-976.

    34. [34]

      (a) X.H. Liu, H.F. Zheng, Y. Xia, et al., Acc. Chem. Res. 50(2017) 2621-2631;
      (b) X.B. Lin, Y. Tang, W. Yang, et al., J. Am. Chem. Soc. 140(2018) 3299-3305;
      (c) X. Lin, W. Yang, W.K. Yang, et al., Angew. Chem. Int. Ed. 58(2019) 13492-13498.

    35. [35]

      L.K. Meng, P. Wu, J. Fang, et al., J. Am. Chem. Soc. 141(2019) 11775-11780.  doi: 10.1021/jacs.9b04619

    36. [36]

      (a) X.F. Xu, C. Li, Z.H. Tao, Y.J. Pan, Green Chem. 19(2017) 1245-1249;
      (b) X.F. Xu, C. Li, M.T. Xiong, et al., Chem. Commun. (Camb. ) 53(2017) 6219-6222;
      (c) X.J. Yan, C. Li, X.F. Xu, et al., Tetrahedron 75(2019) 3081-3087.

    37. [37]

      (a) R. Hommelsheim, Y.J. Guo, Z. Yang, et al., Angew. Chem. Int. Ed. 58(2019) 1203-1207;
      (b) S. Jana, Z. Yang, C. Pei, et al., Chem. Sci. 10(2019) 10129-10134;
      (c) Z. Yang, Y.J. Guo, R.M. Koenigs, Chem. Eur. J. 25(2019) 6703-6706;
      (d) S. Jana, R.M. Koenigs, Asian J. Org. Chem. 8(2019) 683-686;
      (e) C. Empel, R.M. Koenigs, J. Flow Chem. 10(2020) 157-160.

    38. [38]

      J.H. Yang, J.Z. Wang, H.T. Huang, et al., Org. Lett. 21(2019) 2654-2657.  doi: 10.1021/acs.orglett.9b00647

    39. [39]

      K. Orłowska, K. Rybicka-Jasinska, P. Krajewski, D. Gryko, Org. Lett. 22(2020) 1018-1021.  doi: 10.1021/acs.orglett.9b04560

    40. [40]

      (a) J.R. Shi, Y.Y. Li, Y. Li, Chem. Soc. Rev. 46(2017) 1707-1719;
      (b) T. Roy, A.T. Biju, Chem. Commun. (Camb. ) 54(2018) 2580-2594;
      (c) T. Matsuzawa, S. Yoshida, T. Hosoya, Tetrahedron Lett. 59(2018) 4197-4208;
      (d) Y.W. Zeng, J.B. Hu, Synthesis 48(2016) 2137-2150;
      (e) H. Yoshida, K. Takaki, Synlett 23(2012) 1725-1732;
      (f) D.B. Werz, A.T. Biju, Angew. Chem. Int. Ed. 59(2020) 3385-3398.

    41. [41]

      (a) J.H. Chen, V. Palani, T.R. Hoye, J. Am. Chem. Soc. 138(2016) 4318-4321;
      (b) X. Xiao, T.R. Hoye, Nat. Chem. Biol. 10(2018) 838-844;
      (c) S.P. Ross, T.R. Hoye, Nat. Chem. Biol. 9(2017) 523-530.

    42. [42]

      Y.M. Li, C. Mück-Lichtenfeld, A. Studer, Angew. Chem. Int. Ed. 55(2016) 14435-14438.  doi: 10.1002/anie.201608144

    43. [43]

      (a) X.B. Xu, Z.H. Lin, Y.Y. Liu, et al., Org. Biomol. Chem. 15(2017) 2716-2720;
      (b) M. Thangaraj, R.N. Gaykar, T. Roy, A.T. Biju, J. Org. Chem. 82(2017) 4470-4476;
      (c) J.J. Tan, T.Y. Zheng, K. Xu, C.Y. Liu, Org. Biomol. Chem. 15(2017) 4946-4950.

    44. [44]

      T.Y. Zheng, J.J. Tan, R. Fan, et al., Chem. Commun. (Camb. ) 54(2018) 1303-1306.  doi: 10.1039/C7CC08553B

    45. [45]

      (a) R. Fan, B.B. Liu, T.Y. Zheng, et al., Chem. Commun. (Camb. ) 54(2018) 7081-7084;
      (b) H. Jian, Q. Wang, W.H. Wang, et al., Tetrahedron 74(2018) 2876-2883.

    46. [46]

      W.H. Ding, A.M. Yu, L. Zhang, X.T. Meng, Org. Lett. 21(2019) 9014-9018.  doi: 10.1021/acs.orglett.9b03417

    47. [47]

      (a) F.L. Liu, J.R. Chen, Y.Q. Zou, Q. Wei, W.J. Xiao, Org. Lett. 16(2014) 3768-3771;
      (b) H.Y. Li, L.J. Xing, M.M. Lou, et al., Org. Lett. 17(2015) 1098-1101;
      (c) H. Hazatika, K. Neog, A. Sharma, et al., J. Org. Chem. 84(2019) 5846-5854;
      (d) Y.M. Li, A. Studer, Org. Lett. 19(2017) 666-669;
      (e) Y.Y. Li, D.C. Qiu, R.R. Gu, et al., J. Am. Chem. Soc. 138(2016) 10814-10817;
      (f) X.J. Li, Y. Sun, X. Huang, et al., Org. Lett. 19(2017) 838-841;
      (g) T. Matsuzawa, K. Uchida, S. Yoshida, T. Hosoya, Org. Lett. 19(2017) 5521-5524;
      (h) D.L. Chen, Y. Sun, M.Y. Chen, et al., Org. Lett. 21(2019) 3986-3989.

    48. [48]

      (a) X.H. Ye, J. Wang, S.T. Ding, et al., Chem. Eur. J. 23(2017) 10506-10510;
      (b) J. Wang, S.Y. Zhang, C. Xu, et al., Angew. Chem. Int. Ed. 57(2018) 6915-6920.

    49. [49]

      A. Parodi, S. Battaglioli, Y. Liu, et al., Chem. Commun. (Camb. ) 55(2019) 9669-9672.  doi: 10.1039/C9CC04302K

    50. [50]

      Z.Q. He, F.F. Song, H. Sun, Y. Huang, J. Am. Chem. Soc. 140(2018) 2693-2699.  doi: 10.1021/jacs.8b00380

    51. [51]

      M.T. Taylor, J.E. Nelson, M.G. Suero, M.J. Gaunt, Nature 562(2018) 563-568.  doi: 10.1038/s41586-018-0608-y

    52. [52]

      (a) D.Y. Qian, J.W. Sun, Chem. Eur. J. 25(2019) 3740-3751;
      (b) V. Iaroshenko, Organophosphorus Chemistry: From Molecules to Applications, Wiley-VCH, Weinheim, 2019;
      (c) A. Golandaj, A. Ahmad, D. Ramjugernath, Adv. Synth. Catal. 359(2017) 3676-3706;
      (d) K. Ishihara, Proc. Jpn. Acad., Ser. B, Phys. Biol. Sci. 85(2009) 290-313;
      (e) C.Q. He, C.C. Lam, P.Y. Yu, et al., J. Org. Chem. 85(2020) 2618-2625;
      (f) T. Nakamura, K. Okuno, R. Nishiyori, S. Shirakawa, Chem. Asian J. 15(2020) 463-472.

    53. [53]

      S. kaneko, Y. Kumatabara, S. Shimizu, et al., Chem. Commun. (Camb. ) 53(2017) 119-122.  doi: 10.1039/C6CC08411G

    54. [54]

      (a) J.J. Tan, N. Yasuda, Org. Process Res. Dev. 19(2015) 1731-1746;
      (b) K. Maruoka, Proc. Jpn. Acad., Ser. B: Phys. Biol. Sci. 95(2019) 1-16;
      (c) R.J. Fox, J. Qiu, Org. Process Res. Dev. 24(2020) 235-241.

    55. [55]

      S.Y. Liu, K. Maruoka, S. Shirakawa, Angew. Chem. Int. Ed. 56(2017) 4819-4823.  doi: 10.1002/anie.201612328

    56. [56]

      (a) J. Yoshida, A. Shimizu, Y. Ashikari, et al., Bull. Chem. Soc. Jpn. 88(2015) 763-775;
      (b) S. Suga, K. Matsumoto, K. Ueoka, J. Yoshida, J. Am. Chem. Soc. 128(2006) 7710-7711;
      (d) Y. Ashikari, T. Nokami, J. Yoshida, J. Am. Chem. Soc. 133(2011) 11840-11843;
      (e) R. Hayashi, A. Shimizu, J. Yoshida, J. Am. Chem. Soc. 138(2016) 8400-8403;
      (f) R. Hayashi, A. Shimizu, J.A. Davies, et al., Angew. Chem. Int. Ed. 57(2018) 12891-12895.

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