Domino reactions based on Pd-catalyzed C-H bond activation

Progress in Chemistry

Volumn 24, Issue 7, 2012, Pages 1324-1336

  Shen, Jinhai ^a   Cheng, Guolin ^a   Cui, Xiuling ^a  

^a HUAQIAO UNIVERSITY   (China)

Author keywords

C H activation; Domino reaction; Organic synthesis; Palladium catalyst

Indexed keywords

EID: 84866176396     PISSN: 1005281X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (63)

1. Wender P A, Miller B L. Nature, 2009, 460(7252): 197-201
2. Tietze L F. Chem. Rev., 1996, 96(1): 115-136
3. Tietze L F, Brasche G, Gericke K M. Domino Reactions in Organic Synthesis. Weinheim: Wiley-VCH, 2006
4. Heck R F. Comprehensive Organic Synthesis, Vol. 4 (eds. Trost B M, Fleming I). Oxford: Pergamon, 1991. 833
5. Trost B M, Crawley M L. Chem. Rev., 2003, 103: 2921-2944
6. Tamao K, Kiso Y, Sumitani K, Kumada M. J. Am. Chem. Soc., 1972, 94(26): 9268-9269
7. Stille J K. Angew. Chem. Int. Ed., 1986, 25: 508-524
8. Negishi E I, Hu Q, Huang Z, Qian M, Wang G. Aldrichimica Acta, 2005, 38: 71-88
9. Miyaura N, Suzuki A. Chem. Rev., 1995, 95: 2457-2483
10. Tamejiro H. J. Organomet. Chem., 2002, 653(1/2): 58-61
11. Chen X, Engle K M, Wang D H, Yu J Q. Angew. Chem. Int. Ed., 2009, 48(28): 5094-5115
12. Shi Z J. Prog. Chem., 2010, 22(7): 1414-1433
13. Lyons T W, Sanford M S. Chem. Rev., 2010, 110: 1147-1169
14. Le Bras J, Muzart J.Chem. Rev., 2011, 111(3): 1170-1214
15. Negishi E, de Meijere A. Handbook of Organopalladium Chemistry for Organic Synthesis. John Wiley & Sons Inc., 2002
16. Han X L, Liu G X, Lu X Y. Org. Chem., 2005, 25(10): 1182-1197
17. Shindoh N, Takemoto Y, Takasu K. Chem. Eur. J., 2009, 15(45): 12168-12179
18. Oestreich M. The Mizoroki-Heck Reaction. John Wiley & Sons Inc., 2009. 1-42
19. Furuta T, Asakawa T, Iinuma M, Fujii S, Tanaka K, Kan T. Chem. Commun., 2006, 3648-3650
20. Ruck K T, Huffman M A, Kim M M, Shevlin M, Kandur W V, Davies I W. Angew. Chem. Int. Ed., 2008, 47(25): 4711-4714
21. Satyanarayana G, Maichle-Moessmer C, Maier M E. Chem. Commun., 2009, 1571-1573
22. Hu Y, Yu C, Ren D, Hu Q, Zhang L, Cheng D. Angew. Chem. Int. Ed., 2009, 48(30): 5448-5451
23. Hu Y, Ouyang Y, Qu Y, Hu Q, Yao H. Chem. Commun., 2009, 4575-4577
24. Hu Y, Ken D, Zhang L, Lin X, Wan J. Eur. J. Org. Chem., 2010, 4454-4459
25. Kené O, Lapointe D, Eagnou K. Org. Lett., 2009, 11(20): 4560-4563
26. Zeni G, Larock K C. Chem. Rev., 2004, 104(5): 2285-2310
27. Lu Z, Hu C, Guo J, Li J, Cui Y, Jia Y. Org. Lett., 2009, 12(3): 480-483
28. Kim J N, Kim H S, Gowrisankar S, Kim S H. Tetrahedron Lett., 2008, 49(24): 3858-3861
29. Cacchi S, Fabrizi G. Carbopalladation of Alkynes Followed by Trapping with Nucleophilic Reagents. John Wiley & Sons Inc., 2002. 133
30. Zhao J, Larock C. Org. Lett., 2005, 7(4): 701-704
31. Pinto A, Neuville L, Retailleau P, Zhu J P. Org. Lett., 2006, 8 (21): 4927-4930
32. Zhu J P, Pinto A, Neuville L. Angew. Chem. Int. Ed., 2007, 46(18): 3291-3295
33. Tietze L F, Lotz F. Eur. J. Org. Chem., 2006, 4676-4684
34. Herrmann W A, Brossmer C, Fele K, Reisinger C P, Priermeier T, Beller M, Fischer H. Angew. Chem. Int. Ed., 1995, 34(17): 1844-1848
35. Duan Z, Huang U N, Li J, Zhao W N, Mei Y K. Org. Biomol. Chem., 2011, 9(14): 5036-5038
36. Catellani M, Motti E, Della Ca N. Acc. Chem. Res., 2008, 41(11): 1512-1522
37. Maestri G, Larraufie M H, Herat E, Ollivier C, Fensterbank L, Laeote E, Malaeria M. Org. Lett., 2010, 12(24): 5692-5695
38. Martins A, Mariampillai K, Lautens M. Top. Curr. Chem., 2010, 292: 1-33
39. Catellani M, Della Ca N, Maestri G. Chem.-Eur. J., 2009, 15(32): 7850-7853
40. Catellani M, Maestri G, Della Ca N. Chem. Commun., 2009, 4892-4894
41. Lautens M, Zhao Y K, Mariampillai K, Candito D A, Laleu K, Li M Z. Angew. Chem. Int. Ed., 2009, 48(10): 1849-1852
42. Sole D, Serrano O. J. Org. Chem., 2008, 73(23): 9372-9378
43. Catellani M, Motti E, Della Ca N, Deledda S, Fava E, Paneiroli F. Chem. Commun., 2010, 4291-4293
44. Thansandote P, Chong E, Feldmann K O, Lautens M. J. Org. Chem., 2010, 75(10): 3495-3498
45. Cárdenas D J, Martín-Matute K, Feliavarren A M. J. Am. Chem. Soc., 2006, 128(15): 5033-5040
46. García-Cuadrado D, Kraga A A C, Maseras F, Echavarren A M. J. Am. Chem. Soc., 2006, 128(4): 1066-1067
47. Maestri G, Motti E, Della Ca N, Malacria M, Derat E, Catellani M. J. Am. Chem. Soc., 2011, 133(22): 8574-8585
48. Dyker G. Angew. Chem. Int. Ed., 1992, 31(8): 1023-1025
49. Dyker G. Angew. Chem. Int. Ed., 1994, 33(1): 103-105
50. Dyker G. J. Org. Chem., 1993, 58(23): 6426-6428
51. Dyker G, Nerenz F, Siemsen P, Kubenitsehek P, Jones P G. Chem. Ker., 1996, 129: 1265-1269
52. Mauleon P, Alonso I, Carretero J C. Angew. Chem. Int. Ed., 2001, 40(7): 1291-1293
53. Thirunavukkarasu V S, Parthasarathy K, Cheng C H. Angew. Chem. Int. Ed., 2008, 47(49): 9462-9465
54. Thirunavukkarasu V S, Parthasarathy K, Cheng C H. Chem. Eur. J., 2010, 16(5): 1436-1440
55. Gandeepan P, Parthasarathy K, Cheng C H. J. Am. Chem. Soc., 2010, 132(25): 8569-8571
56. Wu Y T, Huang K H, Shin C C, Wu T C. Chem. Eur. J., 2008, 14(22): 6697-6703
57. Wang N X, Tang S, Peng P, Pi S F, Liang Y, Li J H. Org. Lett., 2008, 10(6): 1179-1182
58. Jiao L, Bach T. J. Am. Chem. Soc., 2011, 133(33): 12990-12993
59. Cant A A, Roberts L, Greaney M F. Chem. Commun., 2010, 8671-8673
60. Wu J L, Cui X L, Mi X, Li Y, Wu Y J. Chem. Commun., 2010, 6771-6773
61. Wang J, Wang L, Peng S Y. Chem. Commun., 2011, 5422-5424
62. Zhang J L, Liu R R. Adv. Synth. Catal., 2011, 353(1): 36-40
63. Lautens M, Blanchot M, Candito D A, Larnaud F. Org. Lett., 2011, 13(6): 1486-1489