Citation: Ding Gang, Wang Zeyu, Yin Zhongqiong, Yue Guizhou. Progress in Palladium-Catalyzed Tandem Reaction of Constructing Benzo-Five-Membered Heterocycles[J]. Chinese Journal of Organic Chemistry, ;2015, 36(1): 43-59. doi: 10.6023/cjoc201508012 shu

Progress in Palladium-Catalyzed Tandem Reaction of Constructing Benzo-Five-Membered Heterocycles

Ding Gang ^a,b ,
Wang Zeyu ^a ,
Yin Zhongqiong ^c ,
Yue Guizhou ^a,b,*,,

a.
College of Science, Sichuan Agricultural University, Ya'an, 625014
b.
College of Agricultural Sciences, Sichuan Agricultural University, Chengdu 611130
c.
College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130

Corresponding author: Yue Guizhou, yueguizhou@sicau.edu.cn
Received Date: 10 August 2015
Revised Date: 2 November 2015

Fund Project: the Science & Technology Department of Sichuan Province 2012JY0118

Figures(37)

The benzo-five-membered heterocycles existed extensively in many important natural products and also showed excellent bioactivites. Therefore, organic chemists around the world made efforts to develop the highly efficient methods of constructing these heterocycles. Recently, the syntheses of them via transition metal-catalyzed tandem reaction, especially palladium-catalyzed reaction, have been reported widely. This review emphasizes on the palladium-catalyzed tandem reaction of the formation of benzo-five-membered heterocycles and their derivatives reported since 2000.
- heterocycle,
- tandem reaction,
- palladium catalyst,
- synthesis
1. [1]
  Luize, P. S.; Ueda-Nakamura, T.; Filho, B. P. D.; Cortez, D. A. G.; Nakamura, C. V. Biol. Pharm. Bull. 2006, 29, 2126. doi: 10.1248/bpb.29.2126
2. [2]
  Galliford, C. V.; Scheidt, K. A. Angew. Chem., Int. Ed. 2007, 46, 8748. doi: 10.1002/(ISSN)1521-3773
3. [3]
  Li, H.; Ding, C.; Xu, B.; Hou, X. Acta Chim. Sinica 2014, 72, 765 (in Chinese). doi: 10.6023/A14040329
4. [4]
  Liu, J.; Zhu, Q.; Du, J.; Zhang, X. Chin. J. Org. Chem. 2015, 35, 15 (in Chinese). doi: 10.6023/cjoc201408014
5. [5]
  Ni, C.; Shen, A.; Cao, Y.; Ye, X. Chin. J. Org. Chem. 2014, 34, 278 (in Chinese). doi: 10.6023/cjoc201308031
6. [6]
  Ni, C.; Zhu, L.; Hu, J. Acta Chim. Sinica 2015, 73, 90 (in Chinese). doi: 10.6023/A14110758
7. [7]
  Xiao, Y.; Pan, Q.; Zhang, X. Acta Chim. Sinica 2015, 73, 383 (in Chinese). doi: 10.6023/A15010042
8. [8]
  Zhang, J.; Lu, Q.; Liu, C.; Lei, A. Chin. J. Org. Chem. 2015, 35, 743 (in Chinese). doi: 10.6023/cjoc201411028
9. [9]
  Zhang, Y.; Feng, B. Chin. J. Org. Chem. 2014, 34, 2406 (in Chinese). doi: 10.6023/cjoc201408030
10. [10]
  Bai, D.; Li, C.; Li, J.; Jia, X. Chin. J. Org. Chem. 2012, 32, 994 (in Chinese). doi: 10.6023/cjoc1202073
11. [11]
  Fang, S.; Lü, M.; Long, Y.; Yang, D. Chin. J. Org. Chem. 2011, 31, 1573 (in Chinese).
12. [12]
  Tang, S.; Liang, Y.; Liu, W.-J.; Li, J.-H. Chin. J. Org. Chem. 2004, 24, 1133 (in Chinese).
13. [13]
  Wang, N. Chin. J. Org. Chem. 2011, 31, 1319 (in Chinese).
14. [14]
  Culkin, D. A.; Hartwig, J. F. Acc. Chem. Res. 2003, 36, 234. doi: 10.1021/ar0201106
15. [15]
  Ritleng, V.; Sirlin, C.; Pfeffer, M. Chem. Rev. 2002, 102, 1731. doi: 10.1021/cr0104330
16. [16]
  Gang, F.; Xu, G.; Dong, T.; Yang, L.; Du, Z. Chin. J. Org. Chem. 2015, 35, 1428 (in Chinese). doi: 10.6023/cjoc201502020
17. [17]
  Sheng, R.-L.; Tang, S.; Zhou, D.; Li, Z.-H.; Fu, M.-J.; Jie, L.; Li, S.-H. Synthesis 2015, 47, 1567. doi: 10.1055/s-00000084
18. [18]
  Gansauer, A.; Hildebrandt, S.; Michelmann, A.; Dahmen, T.; von Laufenberg, D.; Kube, C.; Fianu, G. D.; Flowers, R. A. Angew. Chem., Int. Ed. 2015, 54, 7003. doi: 10.1002/anie.201501955
19. [19]
  Wei, X.-H.; Wu, Q.-X.; Yang, S.-D. Synlett 2015, 26, 1417. doi: 10.1055/s-00000083
20. [20]
  Fu, W.; Xu, F.; Fu, Y.; Zhu, M.; Yu, J.; Xu, C.; Zou, D. J. Org. Chem. 2013, 78, 12202. doi: 10.1021/jo401894b
21. [21]
  Grigg, R.; Sansano, J. M.; Santhakumar, V.; Sridharan, V.; Thangavelanthum, R.; Thornton-Pett, M.; Wilson, D. Tetrahedron 1997, 53, 11803. doi: 10.1016/S0040-4020(97)00754-0
22. [22]
  Grigg, R.; Sridharan, V. Tetrahedron 1999, 576, 65.
23. [23]
  Wei, H.-L. Ph.D. Dissertation, Lanzhou University, Lanzhou, 2010 (in Chinese).
24. [24]
  Shen, J.; Cheng, G.; Cui, X. Prog. Chem. 2012, 24, 1324 (in Chinese).
25. [25]
  Li, J.-H.; Song, R.-J.; Liu, Y.; Xie, Y.-X. Synthesis 2015, 47, 1195. doi: 10.1055/s-00000084
26. [26]
  Fretwell, P.; Grigg, R.; Sansano, J. M.; Sridharan, V.; Sukirthalingam, S.; Wilsona, D.; Redpathb, J. Tetrahedron 2000, 56, 7525. doi: 10.1016/S0040-4020(00)00659-1
27. [27]
  Casaschi, A.; Grigg, R.; Sansano, J. M. Tetrahedron 2000, 56, 7553. doi: 10.1016/S0040-4020(00)00661-X
28. [28]
  Jeffery, T. Tetrahedron 1996, 52, 10113. doi: 10.1016/0040-4020(96)00547-9
29. [29]
  Casaschi, A.; Grigg, R.; Sansano, J. M.; Wilsona, D.; Redpathb, J. Tetrahedron 2000, 56, 7541. doi: 10.1016/S0040-4020(00)00660-8
30. [30]
  Grigg, R.; MacLachlan, W. S.; MacPherson, D. T.; Sridharan, V.; Suganthan, S. Tetrahedron 2001, 57, 10335. doi: 10.1016/S0040-4020(01)01061-4
31. [31]
  Anwar, U.; Fielding, M. R.; Grigg, R.; Sridharan, V.; Urch, C. J. J. Org. Chem. 2006, 691, 1476. doi: 10.1016/j.jorganchem.2005.11.045
32. [32]
  Szlosek-Pinaud, M.; Diaz, P.; Martinez, J.; Lamaty, F. Tetrahedron 2007, 63, 3340. doi: 10.1016/j.tet.2007.02.035
33. [33]
  Grigg, R.; Mariani, E.; Sridharan, V. Tetrahedron Lett. 2001, 42, 8677. doi: 10.1016/S0040-4039(01)01811-1
34. [34]
  Szlosek-Pinaud, M.; Diaz, P.; Martinez, J.; Lamaty, F. Tetrahedron Lett. 2003, 44, 8657. doi: 10.1016/j.tetlet.2003.09.169
35. [35]
  Yanada, R.; Obika, S.; Inokuma, T.; Yanada, K.; Yamashita, M.; Ohta, S.; Takemoto, Y. J. Org. Chem. 2005, 70, 6972. doi: 10.1021/jo0508604
36. [36]
  Packer, G.; Lepre, K.; Kankanala, J.; Sridharan, V. RSC Adv. 2014, 4, 3457. doi: 10.1039/C3RA46906A
37. [37]
  Liu, P.; Huang, L.; Lu, Y.; Dilmeghani, M.; Baum, J.; Xiang, T.; Adams, J.; Tasker, A.; Larsen, R.; Faul, M. M. Tetrahedron Lett. 2007, 48, 2307. doi: 10.1016/j.tetlet.2007.01.156
38. [38]
  Kim, H. S.; Lee, H. S.; Kim, S. H.; Kim, J. N. Tetrahedron Lett. 2009, 50, 3154. doi: 10.1016/j.tetlet.2008.11.127
39. [39]
  Day, J.; Frederickson, M.; Hogg, C.; Johnson, C.; Meek, A.; Northern, J.; Reader, M.; Reid, G. Synlett 2015, 26, 2570. doi: 10.1055/s-00000083
40. [40]
  Grigg, R.; Savic, V.; Sridharan, V.; Terrier, C. Tetrahedron 2002, 58, 8613. doi: 10.1016/S0040-4020(02)00763-9
41. [41]
  Jaegli, S.; Erb, W.; Retailleau, P.; Vors, J. P.; Neuville, L.; Zhu, J. Chem. Eur. J.2010, 16, 5863. doi: 10.1002/chem.201000312
42. [42]
  Seashore-Ludlow, B.; Somfai, P. Org. Lett. 2010, 12, 3732. doi: 10.1021/ol1009703
43. [43]
  Liu, X.; Li, B.; Gu, Z. J. Org. Chem.2015, 80, 7547. doi: 10.1021/acs.joc.5b01126
44. [44]
  René, O.; Lapointe, D.; Fagnou, K. Org. Lett. 2009, 11, 4560. doi: 10.1021/ol901799p
45. [45]
  Kim, H. S.; Gowrisankar, S.; Kim, S. H.; Kim, J. N. Tetrahedron Lett. 2008, 49, 3858. doi: 10.1016/j.tetlet.2008.04.080
46. [46]
  Ruck, R. T.; Huffman, M. A.; Kim, M. M.; Shevlin, M.; Kandur, W V.; Davies, I. W. Angew. Chem., Int. Ed. 2008, 47, 4711. doi: 10.1002/(ISSN)1521-3773
47. [47]
  Piou, T.; Neuville, L.; Zhu, J. Angew. Chem., Int. Ed. 2012, 51, 11561. doi: 10.1002/anie.201206267
48. [48]
  Piou, T.; Neuville, L.; Zhu, J. Org. Lett. 2012, 14, 3760. doi: 10.1021/ol301616w
49. [49]
  Piou, T.; Bunescu, A.; Wang, Q.; Neuville, L.; Zhu, J. Angew. Chem., Int. Ed. 2013, 52, 12385. doi: 10.1002/anie.201306532
50. [50]
  Bunescu, A.; Piou, T.; Wang, Q.; Zhu, J. Org. Lett.2015, 17, 334. doi: 10.1021/ol503442n
51. [51]
  Wang, W.; Zhou, R.; Jiang, Z.-J.; Wang, X.; Fu, H.-Y.; Zheng, X.-L.; Chen, H.; Li, R.-X. Eur. J. Org. Chem.2015, 2015, 2579.
52. [52]
  Pinto, A.; Jia, Y.; Neuville, L.; Zhu, J. Eur. Chem. J.2007, 13, 961. doi: 10.1002/(ISSN)1521-3765
53. [53]
  Lee, H.-S.; Kim, K.-H.; Lim, J.-W.; Kim, J.-N. Bull. Korean Chem. Soc. 2011, 32, 1083. doi: 10.5012/bkcs.2011.32.3.1083
54. [54]
  Kamisaki, H.; Yasui, Y.; Takemoto, Y. Tetrahedron Lett. 2009, 50, 2589. doi: 10.1016/j.tetlet.2009.03.100
55. [55]
  Hande, S. M.; Nakajima, M.; Kamisaki, H.; Tsukano, C.; Takemoto, Y. Org. Lett. 2011, 13, 1828. doi: 10.1021/ol2003447
56. [56]
  Newman, S. G.; Lautens, M. J. Am. Chem. Soc. 2011, 133, 1778. doi: 10.1021/ja110377q
57. [57]
  Liu, X.; Ma, X.; Huang, Y.; Gu, Z. Org. Lett.2013, 15, 4814. doi: 10.1021/ol402210a
58. [58]
  Jiang, T. S.; Tang, R. Y.; Zhang, X. G.; Li, X. H.; Li, J. H. J. Org. Chem. 2009, 74, 8834. doi: 10.1021/jo901963g
59. [59]
  Jaegli, S.; Dufour, J.; Wei, H. L.; Piou, T.; Duan, X. H.; Vors, J. P.; Neuville, L.; Zhu, J. Org. Lett. 2010, 12, 4498. doi: 10.1021/ol101778c
60. [60]
  Wu, T.; Mu, X.; Liu, G. Angew. Chem., Int. Ed. 2011, 50, 12578. doi: 10.1002/anie.201104575
61. [61]
  Mu, X.; Wu, T.; Wang, H. Y.; Guo, Y. L.; Liu, G. J. Am. Chem. Soc. 2012, 134, 878. doi: 10.1021/ja210614y
62. [62]
  Kamijo, S.; Sasaki, Y.; Kanazawa, C.; Schüßeler, T.; Yamamoto, Y. Angew. Chem., Int. Ed.2005, 44, 7718. doi: 10.1002/(ISSN)1521-3773
63. [63]
  Miura, T.; Toyoshima, T.; Ito, Y.; Murakami, M. Chem. Lett. 2009, 38, 1174. doi: 10.1246/cl.2009.1174
64. [64]
  Miura, T.; Toyoshima, T.; Takahashi, Y.; Murakami, M. Org. Lett. 2009, 11, 2141. doi: 10.1021/ol900759f
65. [65]
  Toyoshima, T.; Mikano, Y.; Miura, T.; Murakami, M. Org. Lett. 2010, 12, 4584. doi: 10.1021/ol101892b
66. [66]
  Lira, R.; Wolfe, J. P. J. Am. Chem. Soc. 2004, 126, 13906. doi: 10.1021/ja0460920
67. [67]
  Schultz, D. M.; Wolfe, J. P. Org. Lett. 2010, 12, 1208. doi: 10.1021/ol902974j
68. [68]
  Thansandote, P.; Hulcoop, D. G.; Langer, M.; Lautens, M. J. Org. Chem.2009, 74, 1673. doi: 10.1021/jo802604g
69. [69]
  Cacchi, S.; Fabrizi, G.; Goggiamani, A.; Sferrazza, A. Org. Biomol. Chem. 2011, 9, 1727. doi: 10.1039/c0ob01052a
70. [70]
  Houlden, C. E.; Bailey, C. D.; Ford, J. G.; Gagne, M. R.; Lloyd-Jones, G. C.; Booker-Milburn, K. I. J. Am. Chem. Soc. 2008, 130, 10066. doi: 10.1021/ja803397y
71. [71]
  Agasti, S.; Maity, S.; Szabo, K. J.; Maiti, D. Adv. Synth. Catal. 2015, 357, 2331. doi: 10.1002/adsc.v357.10
72. [72]
  Pinto, A.; Neuville, L.; Zhu, J. Angew. Chem., Int. Ed.2007, 46, 3291. doi: 10.1002/(ISSN)1521-3773
73. [73]
  Tang, S.; Peng, P.; Pi, S. F.; Liang, Y.; Wang, N. X.; Li, J. H. Org. Lett. 2008, 10, 1179. doi: 10.1021/ol800080w
74. [74]
  Tang, S.; Peng, P.; Wang, Z.-Q.; Tang, B.-X.; Deng, C.-L.; Li, J.-H.; Zhong, P.; Wang, N.-X. Org. Lett. 2008, 10, 1875. doi: 10.1021/ol8006315
75. [75]
  An, G.; Zhou, W.; Zhang, G.; Sun, H.; Han, J.; Pan, Y. Org. Lett. 2010, 12, 4482. doi: 10.1021/ol101664y
76. [76]
  Wang, J. Y.; Su, Y. M.; Yin, F.; Bao, Y.; Zhang, X.; Xu, Y. M.; Wang, X. S. Chem. Commun. 2014, 50, 4108. doi: 10.1039/c3cc49315f
77. [77]
  Nicolai, S.; Erard, S.; Gonzalez, D. F.; Waser, J. Org. Lett. 2010, 12, 384. doi: 10.1021/ol9027286
78. [78]
  Yip, K.-T.; Yang, M.; Law, K.-L.; Zhu, N.-Y.; Yang, D. J. Am. Chem. Soc. 2006, 128, 3130. doi: 10.1021/ja060291x
79. [79]
  Yip, K. T.; Zhu, N. Y.; Yang, D. Org. Lett. 2009, 11, 1911. doi: 10.1021/ol900355h
80. [80]
  He, W.; Yip, K.-T.; Zhu, N.-Y.; Yang, D. Org. Lett. 2009, 11, 5626. doi: 10.1021/ol902348t
81. [81]
  Du, W.; Gu, Q.; Li, Z.; Yang, D. J. Am. Chem. Soc. 2015, 137, 1130. doi: 10.1021/ja5102739
82. [82]
  Mariampillai, B.; Alberico, D.; Bidau, V.; Lautens, M. J. Am. Chem. Soc. 2006, 128, 14436. doi: 10.1021/ja064742p
83. [83]
  Rudolph, A.; Rackelmann, N.; Turcotte-Savard, M.-O.; Lautens, M. J. Org. Chem. 2009, 74, 289. doi: 10.1021/jo802180h
84. [84]
  Wu, X. X.; Zhou, P. X.; Wang, L. J.; Xu, P. F.; Liang, Y. M. Chem. Commun. 2014, 50, 3882. doi: 10.1039/c4cc00809j
85. [85]
  Thansandote, P.; Raemy, M.; Rudolph, A.; Lautens, M. Org. Lett. 2007, 9, 5255. doi: 10.1021/ol702472u
86. [86]
  Muñiz, K. J. Am. Chem. Soc. 2007, 129, 14543.
87. [87]
  Ying, A.-G.; Ye, W.-D.; Liu, L.; Wu, G.-F.; Chen, X.-Z.; Qian, S.; Zhang, Q.-P. Chin. J. Org. Chem. 2008, 28, 2081 (in Chinese).
88. [88]
  John, J.; Indu, U.; Suresh, E.; Radhakrishnan, K. V. J. Am. Chem. Soc.2009, 131, 5402. doi: 10.1021/ja900306m
89. [89]
  Prakash, P.; Jijy, E.; Preethanuj, P.; Pihko, P. M.; Sarath Chand, S.; Radhakrishnan, K. V. Chem. Eur. J. 2013, 19, 10473. doi: 10.1002/chem.v19.32
90. [90]
  Chand, S. S.; Jijy, E.; Prakash, P.; Szymoniak, J.; Preethanuj, P.; Dhanya, B. P.; Radhakrishnan, K. V. Org. Lett. 2013, 15, 3338. doi: 10.1021/ol401374d
91. [91]
  Ramirez, T. A.; Wang, Q.; Zhu, Y.; Zheng, H.; Peng, X.; Cornwall, R. G.; Shi, Y. Org. Lett. 2013, 15, 4210. doi: 10.1021/ol401935c
92. [92]
  Zheng, H.; Zhu, Y.; Shi, Y. Angew. Chem., Int. Ed. 2014, 53, 11280. doi: 10.1002/anie.201405365
93. [93]
  Campbell, C. D.; Greenaway, R. L.; Holton, O. T.; Chapman, H. A.; Anderson, E. A. Chem. Commun. 2014, 50, 5187. doi: 10.1039/C3CC45634J
94. [94]
  Senadi, G. C.; Hu, W. P.; Boominathan, S. S.; Wang, J. J. Chem. Eur. J. 2015, 21, 998. doi: 10.1002/chem.201405933
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