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Progress in Chemistry 2014, Vol. 26 Issue (04): 592-608 DOI: 10.7536/PC130904 Previous Articles   Next Articles

• Review •

Drug Synthesis via C—H Bond Functionalization

Gong Hao, Yang Yiwen, Kuang Chunxiang*   

  1. Department of Chemistry, Tongji University, Shanghai 200092, China
  • Received: Revised: Online: Published:
  • Supported by:

    The work was supported by the National Natural Science Foundation of China (No.21272174)

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The C—H bond functionalization by transition metal is one of the essential contents in organic chemistry. And it has become an enabling tool in the synthesis of drugs. This review describes the classical reactions of C—H bond functionalization and focus on arylation, alkenylation, alkylation, halogenation, hydroxylation, amination, and insertion which provide a simple and rapid way for the drug synthesis. The detail of the applications and relevant mechanisms are also described. Finally we look forward to its development prospects in this field.

Contents
1 Introduction
2 C—C bond formation
2.1 sp2 C—H functionalization assisted by the directing group
2.2 sp2 C—H functionalization without the directing group
2.3 sp3 C—H functionalization assisted by the directing group
2.4 sp3 C—H functionalization without the directing group
3 C—H insertion
4 C—X bond formation
4.1 C—X bond formation assisted by the directing group
4.2 C—X bond formation without the directing group
5 Conclusion and outlook

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[1] Van H R, Verberg G. Trav. Chim. Pays-Bas, 1965, 84: 1263.
[2] Fujiwara Y, Moritani I, Danno S. J. Am. Chem. Soc., 1969, 91: 7166.
[3] Gol’dshleger N F, Tyabin M B, Shilov A E. Zh. Fiz. Khim., 1969, 43: 2174.
[4] 郭兴伟(Guo X W), 李志平(Li Z P), 李朝军(Li C J). 化学进展(Prog. Chem. ), 2010, 22(7): 1434.
[5] Quirk J, Thornton M, Kirkpatrick P. Nature, 2003, 2: 769.
[6] Taber D F, Neubert T D, Rheingold A L. J. Am. Chem. Soc., 2002, 124: 12416.
[7] 刘伟(Liu W. ), 毕艳兰(Bi Y L), 有机化学(Chin. J. Org. Chem. ), 2012, 32: 1041.
[8] Ouellet S G, Roy A, Molinaro C, Angelaud R, Marcoux J F, O’Shea P D, Davies I W. J. Org. Chem., 2011, 76: 1436.
[9] Seki M, Nagahama M. J. Org. Chem., 2011, 76: 10198.
[10] Wang G W, Yuan T T, Li D D. Angew. Chem. Int. Ed., 2011, 50: 1380.
[11] Blanchot M, Candito D A, Larnaud F, Lautens M. Org. Lett., 2011, 13, 6: 1486.
[12] Miao J M, Ge H B. Org. Lett., 2013, 15, 12: 2930.
[13] Wang J, Rosingana M, Watson D J, Discordia R P, Soundarajan N, Li W-S. Tetrahedron Letters, 2001 42: 8935.
[14] Tsuji J. Synthesis, 1984, 369.
[15] Lafrance M, Blaquiere N, Fagnou K. Chem. Commun., 2004, 2874.
[16] Leblanc M, Fagnou K. Org. Lett., 2005, 7, 14: 2849.
[17] Tomori H, Fox J M, Buchwald S L. J. Org. Chem., 2000, 65, 17: 5334.
[18] Vorogushin A V, Predeus A V, Wulff W D, Hansen H J. J. Org. Chem., 2003, 68, 15: 5826.
[19] Gauthier D R, Limanto J, Devine P N, Desmond R A, Szumigala R H J, Foster B S, Volante R P. J. Org. Chem., 2005, 70: 5938.
[20] Lafrance M, Gorelsky S I, Fagnou K. J. Am. Chem. Soc., 2007, 129, 47: 14570.
[21] Caron L, Campeau L C, Fagnou K. Org. Lett., 2008, 10, 20: 4533.
[22] Gaulier S M, McKay R, Swain N A. Tetrahedron Letters, 2011, 52(45): 6000.
[23] Kiser E J, Magano J, Shine R J, Chen M H. Org. Process Res. Dev., 2012, 16, 2: 255.
[24] Hennessy E J, Buchwald S L. J. Am. Chem. Soc., 2003, 125(40): 12084.
[25] 王勇(Wang Y), 程国林(Cheng G L), 崔秀灵(Cui X L). 有机化学(Chin. J. Org. Chem. ), 2012, 32: 2018.
[26] Campeau L C, Rousseaux S, Fagnou K. J. Am. Chem. Soc., 2005, 127: 18020.
[27] Youssif S. ARKIVOC, 2001, (i): 242.
[28] Leclerc J P, Fagnou K. Angew. Chem. Int. Ed., 2006, 45: 7781.
[29] Campeau L C, Bertrand-Laperle M, Leclerc J P, Villemure E, Gorelsky S, Fagnou K. J. Am. Chem. Soc., 2008, 130: 3276.
[30] Campeau L C, Sun H Y, Gorelsky S I, Stuart D R, Fagnou K. J. Org. Chem., 2010, 75: 8180.
[31] Campeau L C, Stuart D R, Leclerc J P, Bertrand-Laperle M, Villemure E, Sun H Y, Lasserre S, Guimond N, Lecavallier M, Fagnou K. J. Am. Chem. Soc., 2009, 131: 3291.
[32] Schipper D J, El-Salfiti M, Whipp C J, Fagnou K. Tetrahedron, 2009, 65: 4977.
[33] Quirk J, Thornton M, Kirkpatrick P. Nature, 2003, 2: 769.
[34] Capdeville R, Buchdunger E, Zimmermann J, Matter A. Nature, 2002, 1: 493.
[35] Friesen R W, Brideau C, Chan C C, Charleson S, DeschênesD, Dubé D, Ethier D, Fortin R, Gauthier J Y, Girard Y, Gordon R, Greig G M, Riendeau D, Savoie C, Wang Z, Wong E, Visco D, Xu L J, Young R N. Biorg. Med. Chem. Lett., 1998, 8, 2777.
[36] Campeau L C, Bertrand-Laperle M, Leclerc J P, Villemure E, Gorelsky S, Fagnou K. J. Am. Chem. Soc., 2008, 130: 3276.
[37] Ye M, Gao G L, Edmunds A J, Worthington P A, Morris J A, Yu J Q. J. Am. Chem. Soc., 2011, 133(47): 19090.
[38] Yokooji A, Okazawa T, Satoh T, Miura M, Nomura M. Tetrahedron, 2003, 59(30): 5685.
[39] Liegault B, Lapointe D, Caron L, Vlassova A, Fagnou K. J. Org. Chem., 2009, 74: 1826.
[40] Joo J M, Touré B B, Sames D. J. Org. Chem., 2010, 75: 4911.
[41] Shibahara F, Yamaguchi E, Murai T. Chem. Commun., 2010, 46: 2471.
[42] Shibahara F, Yamaguchi E, Murai T. J. Org. Chem., 2011, 76: 2680.
[43] Canivet J, Yamaguchi J, Ban I, Itami K. Org. Lett., 2009, 11, 8: 1733.
[44] Yamamoto T, Muto K, Komiyama M, Canivet J, Yamaguchi J, Itami K. Chem. Eur. J., 2011, 17: 10113.
[45] Kirchberg S, Tani S, Ueda K, Yamaguchi J, Studer A, Itami K. Angew. Chem. Int. Ed., 2011, 50, 10: 2387.
[46] Baran P S, Richter J M, Lin D W. Angew. Chem. Int. Ed., 2005, 44: 609.
[47] Jahn U, Harmann P. Chem. Commun., 1998, 2: 209.
[48] Besselivre F, Piguel S, Mahuteau-Betzer F, Grierson D S. Org. Lett., 2008, 10, 18: 4029.
[49] Xu X, Liu Y, Park C M. Angew. Chem. Int. Ed., 2012, 51: 9372.
[50] He G, Chen G. Angew. Chem. Int. Ed., 2011, 50: 5192.
[51] Muratake H, Hayakawa A, Natsume M. Tetrahedron Lett., 1997, 38: 7577.
[52] Martin C L, Overman L E, Rohde J M. J. Am. Chem. Soc., 2008, 130: 7568.
[53] Chaumontet M, Piccardi R, Baudoin O. Angew. Chem. Int. Ed., 2009, 48: 179.
[54] Kirmse W. Angew. Chem. Int. Ed. Engl., 1997, 36: 1164.
[55] Davies L, Beckwith J. Chem. Rev., 2003, 103: 2861.
[56] Astada M, Hashimoto S. Tetrahedron Letters, 1998, 39: 79.
[57] Anada M, Mita O, Watanabe H, Kitagaki S, Hashimoto S. Synlett, 1999, 1775.
[58] Axten J M, Ivy R, Krim L, Winkler J D. J. Am. Chem. Soc., 1999, 121, 27: 6511.
[59] Davies L, Stafford G, Hansen T. Org. Lett., 1999, 1, 2: 233.
[60] Davies L, Walji M, Townsend R J. Tetrahedron Lett., 2002. 43: 4981.
[61] Davies L, Gregg M, Tetrahedron Lett., 2002, 43(28): 4951.
[62] Davies L, Ni A. Chem. Commun., 2006, 3110.
[63] Taber D F, Neubert T D, Rheingold A L. J. Am. Chem. Soc., 2002, 124: 12416.
[64] Yun S Y, Zheng J C, Lee D. J. Am. Chem. Soc., 2009, 131: 8413.
[65] Kodama H, Katsuhira T, Nishida T, Hino T, Tsubata K. WO2001083421A1, 2001.
[66] Mei T S, Wang D H, Yu J Q. Org. Lett., 2010, 12(14): 3140.
[67] Xiao B, Gong T J, Xu J, Liu Z J, Liu L. J. Am. Chem. Soc., 2011, 133: 1466.
[68] Li Y, Ding Y J, Wang J Y, Wang X S. Org. Lett., 2013, 15(11): 2574.
[69] Woodward R B, Heusler K, Gosteli J, Naegeli P, Oppolzer W, Ramage R, Ranganathan S, Vorbruggen H. J. Am. Chem. Soc., 1966, 88, 4: 852.
[70] Wehn P M, Bois J D. J. Am. Chem. Soc., 2002, 124: 12950.
[71] McNeill E, Bois J D. J. Am. Chem. Soc., 2010, 132: 10202.
[72] Bullock K, Chong P, Davis R, Elitzin V, Hatcher M, Jackson M, Liu B, Patterson D, Powers J, Salmons M, Tabet E, Toczko M. Top Catal., 2012, 55: 446.
[73] 王晔峰(Wang Y F), 曾京辉(Zeng J H), 崔晓瑞(Cui X R). 有机化学(Chin. J. Org. Chem)., 2012, 32: 1041.

[1] .  Catalysts Used in Addition Copolymerization of Ethylene and Norbornene [J]. Progress in Chemistry, 2010, 22(10): 2024-2032.
[2] Wu Pingyi,Ji Shengfu**,Hu Linhua,Li Chengyue. Preparation and Catalytic Applications of Transition Metal Assembled into the Channels of Mesoporous Molecular Sieves [J]. Progress in Chemistry, 2007, 19(04): 437-443.
[3] Zhenming Chen1, Jinhua Liu 2, Tao, Junhua2,3**. Biocatalysis for Green Chemistry and Drug Development [J]. Progress in Chemistry, 2007, 19(012): 1919-1927.
[4] Chen Liyi,Yang Haijian,Sun Wenhua**. Advances of Olefin Polymerization in Aqueous Solutions [J]. Progress in Chemistry, 2003, 15(05): 401-.
[5] Shen Haoyu,Jin Guoxin**. New Type Late Transition Metal Catalysts for Olefin Polymerization ——Nickel-based Olefin Polymerization Catalysts [J]. Progress in Chemistry, 2003, 15(01): 60-.