Synthesis 2015; 47(23): 3645-3668
DOI: 10.1055/s-0035-1560646
short review
© Georg Thieme Verlag Stuttgart · New York

Recent Advances in Transition-Metal-Catalyzed Silylations of Arenes with Hydrosilanes: C–X Bond Cleavage or C–H Bond Activation­ Synchronized with Si–H Bond Activation

Zheng Xu*
a   Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Education, Hangzhou Normal University, No 1378, Wenyi West Road, Science Park of HZNU, Hangzhou, P. R. of China   Email: zhengxu@hznu.edu.cn   Email: liwenxu@hznu.edu.cn
,
Wei-Sheng Huang
a   Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Education, Hangzhou Normal University, No 1378, Wenyi West Road, Science Park of HZNU, Hangzhou, P. R. of China   Email: zhengxu@hznu.edu.cn   Email: liwenxu@hznu.edu.cn
,
Jin Zhang
a   Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Education, Hangzhou Normal University, No 1378, Wenyi West Road, Science Park of HZNU, Hangzhou, P. R. of China   Email: zhengxu@hznu.edu.cn   Email: liwenxu@hznu.edu.cn
,
Li-Wen Xu*
a   Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Education, Hangzhou Normal University, No 1378, Wenyi West Road, Science Park of HZNU, Hangzhou, P. R. of China   Email: zhengxu@hznu.edu.cn   Email: liwenxu@hznu.edu.cn
b   State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou, P. R. of China
› Author Affiliations
Further Information

Publication History

Received: 31 July 2015

Accepted after revision: 12 September 2015

Publication Date:
08 October 2015 (online)


Dedicated to Professor Xue-Long Hou on the occasion of his 60th birthday

Abstract

Arylsilanes are valuable organosilicon compounds and attract significant research interest due to their promising applications in organic synthesis. The development of aromatic C–Si cross-coupling reactions represents a major challenge in both organosilicon chemistry and organic synthesis. A number of investigations are focused on developing transition-metal-catalyzed Si–C coupling reactions due to the associated high atom economy and superior functional group compatibility. This review describes recent advances in transition-metal-catalyzed selective silylations of aryl C–H and C–X (X = halide) bonds with hydrosilanes.

1 Introduction

2 Silylation of Arenes with Hydrosilanes via Aryl C–H Bond Activation

2.1 Rhodium-Catalyzed Dehydrogenative Silylations

2.2 Iridium-Catalyzed Dehydrogenative Silylations

2.3 Ruthenium-Catalyzed Dehydrogenative Silylations

2.4 Platinum-Catalyzed Dehydrogenative Silylations

2.5 Other Transition-Metal-Catalyzed Dehydrogenative Silylations

3 Silylation of Arenes with Hydrosilanes via Aryl C–X Bond Cleavage

3.1 Palladium-Catalyzed Silylations of Aryl Halides

3.2 Rhodium-Catalyzed Silylations of Aryl Halides

3.3 Platinum-Catalyzed Silylations of Aryl Halides

4 Conclusion

 
  • References

    • 1a Schranck J, Tlili A, Beller M. Angew. Chem. Int. Ed. 2014; 53: 9426
    • 1b Toutov AA, Liu WB, Betz KN, Fedorov A, Stoltz BM, Grubbs RH. Nature 2015; 518: 80
  • 2 Kakiuchi F, Kochi T, Murai S. Synlett 2014; 25: 2390
  • 3 Cheng C, Hartwig JF. Chem. Rev. 2015; 115: 8946
  • 4 Kuhl N, Hopkinson MN, Wencel-Delord J, Glorius F. Angew. Chem. Int. Ed. 2012; 51: 10236
  • 5 Mo J, Wang L, Liu Y, Cui X. Synthesis 2015; 47: 439
  • 6 Shintani R. Asian J. Org. Chem. 2015; 4: 510
  • 7 Hartwig JF. Acc. Chem. Res. 2012; 45: 864
  • 8 Choi J, Goldman AS In Iridium Catalysis . Andersson PG. Springer; Heidelberg: 2011
  • 9 Xu Z, Xu L.-W. ChemSusChem 2015; 8: 2176
  • 10 Sharma R, Kumar R, Kumar I, Singh B, Sharma U. Synthesis 2015; 47: 2347
  • 11 Sakakura T, Tokunaga Y, Sodeyama T, Tanaka M. Chem. Lett. 1987; 16: 2375
  • 12 Ezbiansky K, Djurovich PI, LaForest M, Sinning DJ, Zayes R, Berry DH. Organometallics 1998; 17: 1455
  • 13 Cheng C, Hartwig JF. Science 2014; 343: 853
  • 14 Cheng C, Hartwig JF. J. Am. Chem. Soc. 2014; 136: 12064
  • 15 Ureshino T, Yoshida T, Kuninobu Y, Takai K. J. Am. Chem. Soc. 2010; 132: 14324
  • 16 Xu L.-W. Angew. Chem. Int. Ed. 2012; 51: 12932
  • 17 Xu L.-W, Li L, Lai G.-Q, Jiang J.-X. Chem. Soc. Rev. 2011; 40: 1777
  • 18 Kuninobu Y, Yamauchi K, Tamura N, Seiki T, Takai K. Angew. Chem. Int. Ed. 2013; 52: 1520
  • 19 Shibata T, Shizuno T, Sasaki T. Chem. Commun. 2015; 51: 7802
  • 20 Zhang Q.-W, An K, Liu L.-C, Yue Y, He W. Angew. Chem. Int. Ed. 2015; 54: 6918
  • 21 Murai M, Matsumoto K, Takeuchi Y, Takai K. Org. Lett. 2015; 17: 3102
  • 22 Lee T, Wilson TW, Berg R, Ryberg P, Hartwig JF. J. Am. Chem. Soc. 2015; 137: 6742
  • 23 Gustavson WA, Epstein PS, Curtis MD. Organometallics 1982; 1: 884
  • 24 Saiki T, Nishio Y, Ishiyama T, Miyaura N. Organometallics 2006; 25: 6068
  • 25 Ishiyama T, Sato K, Nishio Y, Miyaura N. Angew. Chem. Int. Ed. 2003; 42: 5346
  • 26 Ishiyama T, Sato K, Nishio Y, Saiki T, Miyaura N. Chem. Commun. 2005; 5065
  • 27 Lu B, Falck JR. Angew. Chem. 2008; 120: 7618
  • 28 Simmons EM, Hartwig JF. J. Am. Chem. Soc. 2010; 132: 17092
  • 29 Kuznetsov A, Onishi Y, Inamoto Y, Gevorgyan V. Org. Lett. 2013; 15: 2498
  • 30 Choi G, Tsurugi H, Mashima K. J. Am. Chem. Soc. 2013; 135: 13149
  • 31 Ishiyama T, Saiki T, Kishida E, Sasaki I, Ito H, Miyaura N. Org. Biomol. Chem. 2013; 11: 8162
  • 32 Cheng C, Hartwig JF. J. Am. Chem. Soc. 2015; 137: 592
  • 33 Murai M, Takami K, Takai K. Chem. Eur. J. 2015; 21: 4566
  • 34 Murai M, Takami K, Takeshima H, Takai K. Org. Lett. 2015; 17: 1798
  • 35 Wakaki T, Kanai M, Kuninobu Y. Org. Lett. 2015; 17: 1758
  • 36 Kakiuchi F, Igi K, Matsumoto M, Chatani N, Murai S. Chem. Lett. 2001; 422
  • 37 Kakiuchi F, Matsumoto M, Tsuchiya K, Igi K, Hayamizu T, Chatani N, Murai S. J. Organomet. Chem. 2003; 686: 134
  • 38 Sakurai T, Matsuoka Y, Hanataka T, Fukuyama N, Namikoshi T, Watanabe S, Murata M. Chem. Lett. 2012; 41: 374
  • 39 Takada K, Hanataka T, Namikoshi T, Watanabe S, Murata M. Adv. Synth. Catal. 2015; 357: 2229
  • 40 Ihara H, Suginome M. J. Am. Chem. Soc. 2009; 131: 7502
  • 41 Mita T, Tanaka H, Michigami K, Sato Y. Synlett 2014; 25: 1291
  • 42 Mita T, Michigami K, Sato Y. Org. Lett. 2012; 14: 3462
  • 43 Klare HF. T, Oestreich M, Ito J, Nishiyama H, Ohki Y, Tatsumi K. J. Am. Chem. Soc. 2011; 133: 3312
  • 44 Omann L, Oestreich M. Angew. Chem. Int. Ed. 2015; 54: 10276
  • 45 Uchimaru Y, El Sayed AM. M, Tanaka M. Organometallics 1993; 12: 2065
  • 46 Tsukada N, Hartwig JF. J. Am. Chem. Soc. 2005; 127: 5022
  • 47 Murata M, Fukuyama N, Wada J, Watanabe S, Masuda Y. Chem. Lett. 2007; 36: 910
    • 48a Kakiuchi F, Tanaka Y, Chatani N, Murai S. J. Organomet. Chem. 1993; 456: 45
    • 48b Sunada Y, Soejima H, Nagashima H. Organometallics 2014; 33: 5936
  • 49 Oyamada J, Nishiura M, Hou Z. Angew. Chem. Int. Ed. 2011; 50: 10720
  • 50 Murata M, Suzuki K, Watanabe S, Masuda Y. J. Org. Chem. 1997; 62: 8569
  • 51 Boukherroub R, Chatgilialoglu C, Manuel G. Organometallics 1996; 15: 1508
  • 52 Manoso AS, DeShong P. J. Org. Chem. 2001; 66: 7449
  • 53 Denmark SE, Kallemeyn JM. Org. Lett. 2003; 5: 3483
  • 54 Murata M, Ohara H, Oiwa R, Watanabe S, Masuda Y. Synthesis 2006; 1771
  • 55 Murata M, Ota K, Yamasaki H, Watanabe S, Masuda Y. Synlett 2007; 1387
  • 56 Gu W, Liu S, Silverman RB. Org. Lett. 2002; 4: 4171
  • 57 Iranpoor N, Firouzabadi H, Azadi R. J. Organomet. Chem. 2010; 695: 887
  • 58 Yamanoi Y. J. Org. Chem. 2005; 70: 9607
  • 59 Yamanoi Y, Taira T, Sato J, Nakamula I, Nishihara H. Org. Lett. 2007; 9: 4543
  • 60 Lesbani A, Kondo H, Yabusaki Y, Nakai M, Yamanoi Y, Nishihara H. Chem. Eur. J. 2010; 16: 13519
  • 61 Kurihara Y, Yamanoi Y, Nishihara H. Chem. Commun. 2013; 49: 11275
  • 62 Kurihara Y, Nishikawa M, Yamanoi Y, Nishihara H. Chem. Commun. 2012; 48: 11564
  • 63 Lesbani A, Kondo H, Sato J, Yamanoi Y, Nishihara H. Chem. Commun. 2010; 46: 7784
  • 64 Iizuka M, Kondo Y. Eur. J. Org. Chem. 2008; 2008: 1161
  • 65 Murata M, Ishikura M, Nagata M, Watanabe S, Masuda Y. Org. Lett. 2002; 4: 1843
  • 66 Murata M, Yamasaki H, Ueta T, Nagata M, Ishikura M, Watanabe S, Masuda Y. Tetrahedron 2007; 63: 4087
  • 67 Murata M, Yamasaki H, Uogishi K, Watanabe S, Masuda Y. Synthesis 2007; 2944
  • 68 Yamanoi Y, Nishihara H. Tetrahedron Lett. 2006; 47: 7157
  • 69 Yamanoi Y, Nishihara H. J. Org. Chem. 2008; 73: 6671
  • 70 Hamze A, Provot O, Alami M, Brion J.-D. Org. Lett. 2006; 8: 931