Progress in Preparation of α-Arylpropionic Acids through Catalytic Carbonylation

Progress in Chemistry

Volumn 13, Issue 1, 2001, Pages 43-47

  Xie, Baohan ^a   Zhang, Yuhua ^a  

^a LANZHOU INSTITUTE OF CHEMICAL PHYSICS   (China)

Author keywords

arylpropionic acid; Anti inflammatory drug; Catalytic carbonylation

Indexed keywords

EID: 0347122237     PISSN: 1005281X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (68)

1. Rieu J P, Boucherle A, Cousse H, Mouzin G. Tetrahedron, 1986, 42: 4095
2. Shen T Y. Angew. Chem., Int. Ed. Engl., 1972, 6: 460
3. Hutt A J, Caldwell J. Clin. Pharmacokinet., 1984, 9: 371
4. Harrison I T. J. Med. Chem., 1970, 13: 203
5. Harrington R J, Londewijk E. Org. Process Res. & Develop., 1997, 1(1):72
6. Scrivanti A, Matteoli U. Tetrahydron Lett., 1995, 36(49): 9015
7. Ponec V. J. Mol. Cat., A: Chemical, 1998, 133(3): 221
8. Tsuji J, Mandai T. Angew. Chem., Int. Ed. Eng., 1996, 34 (23-24): 2589
9. Monflier E, Mortreux A. Cat. Lett., 1998, 50(1-2):115
10. Goedheijt M S, Kamer P C J, Leeuwen P W N M. J. Mol. Cat., A: Chemical, 1998, 134(1-3): 243
11. Elango V, Davenport K G, Murphy M A, et al. EP 400 892, 1990 (Chem. Abstr., 1990, 114: 206780k)
12. Elango V, Murphy M A, Smith B L, et al. EP 284 310, 1988 (Chem. Abstr., 1988,110:153916t)
13. Tanaka Y, Kojima H, Tsuji Y. GB 21 99 030, 1988 (Chem. Abstr., 1988,109:212807n)
14. Sheldon R A. Chemtech., 1994, 24: 38
15. Mott G N, Zey E G. EP 337 803, 1989 (Chem. Abstr., 1989,112: 234979j)
16. Jang E J, Lee K H, Lee J S, Kim Y G. J. Mol. Cat. A: Chemical, 1999, 138: 25
17. Tanaka Y, Kojima H. JP 88 162 658, 1988(Chem. Abstr., 1988, 110: 172881u)
18. Papadogianakis G, Maat L, Sheldon R A. J. Chem. Tech. Biotechnol., 1997, 70: 83
19. (Mitsubishi Petrochemical Co., Ltd.). JP 8 498 037, 1984 (Chem. Abstr., 1984, 101: 151606g); JP 8 495 239, 1984(Chem. Abstr., 1984, 101: 170908y)
20. (Mitsubishi Petrochemical Co., Ltd.). JP 8 498 037, 1984 (Chem. Abstr., 1984, 101: 151606g); JP 8 495 239, 1984(Chem. Abstr., 1984, 101: 170908y)
21. Baird J M, Kern J R, Lee G R, et al. J.Org. Chem., 1991, 56:1928
22. (Xie B H), (Xia C G), (Kou Y), (Yin Y Q), (Lu S J). CN 1 221 729A, 1997
23. Zhou H, Chen J, Lu S et al. J. Organomet. Chem., 1998, 566: 239
24. Xie B H, Xia C G, Lu S J, et al. Terahedron Lett., 1998, 39 (40): 7365
25. Elango V. EP 338 852, 1989 (Chem. Abstr., 1989, 113: 40159s)
26. Stahly B C, Lin R W, Atkinson E E. US 4 990 658, 1989 (Chem. Abstr., 1989, 114: 246962c)
27. Wu T C, US 5 322 959, 1994 (Chem. Abstr., 1994, 121: 133704w)
28. Fauvargue J F. Nov. J. Chim., 1986, 10(2): 119
29. Harrison I T. US 3 652 683, 1972 (Chem. Abstr., 1972, 77: 5232f)
30. Francalanci F, Foa M. J. Electroanalyst. Chem., 1982, 232: 59
31. Arzoumanian H, Buono G, Choukrad M, Petrignani J F. Organometallics, 1988, 7: 59
32. Hodge P. Chem. Soc. Rev., 1997, 26(6): 417
33. Shimizu I, Matsumura Y, Tokumoto Y, et al. JP 9 006 424, 1990 (Chem. Abstr., 1990, 113: 171672b)
34. Getman D P, Beck G R, Riley D P. EP 226 566, 1987 (Chem. Abstr., 1987, 108:74987x)
35. Campo P, Petrignani J F, Cocolios P, et al. EP 453 356, 1991 (Chem. Abstr., 1990, 116: 58965y)
36. Shimizu I, Matsumura Y, Tokumoto Y, et al. JP 9 006 431, 1990 (Chem. Abstr., 1990, 113: 5941u)
37. Shimizu I, Matsumura Y, Tokumoto Y, et al. Eur. Pat. Appl. EP 374850, 1990. (Chem. Abstr., 1990, 114: 81238f)
38. Wu T C. US 5 254 720, 1993 (Chem. Abstr., 1993, 120: 106518m)
39. Wu T C. US 5 315 026, 1994 (Chem. Abstr., 1994, 121: 108226j)
40. Takeda M, Uchide M, Iwane H. DE 2 646 792, 1977 (Chem. Abstr., 1977,87: 67848x)
41. Montedison S P A. JP 8 326 841, 1983 (Chem. Abstr., 1983, 99: 22131q)
42. Cometti G, Chiusoli G P. J. Organomet. Chem., 1982, 236: C31
43. Consiglio G, Pino P, Flowers L I, et al. J. Chem. Soc., Chem. Commun., 1983, 612
44. Kollar L, Bakos J, Toth I. J. Organomet. Chem., 1988, 350: 227; 1989, 370: 257
45. Kollar L, Bakos J, Toth I. J. Organomet. Chem., 1988, 350: 227; 1989, 370: 257
46. Stille J K, Parrinello G. J. Am. Chem. Soc., 1987, 109: 7122
47. Stille J K, Parrinello G. J. Mol. Cat., 1983, 21: 203
48. Baker G L, Fritschel S, Stille J K. J. Org. Chem., 1981, 46: 2954
49. Ojima I, Kogure T, Yoda N. J. Org. Chem., 1980, 45: 4728
50. Achiwa K. J. Am. Chem. Soc., 1976, 98:8265
51. Alper H, Nathalie H. J. Am. Chem. Soc., 1990, 112: 2803
52. Namel N, Alper H. J. Chem. Soc., Chem. Commun., 1990, 135
53. Zhou H Y, Hou J G, Chen J, et al. Organomet. Chem., 1997, 543:227
54. Harrison I T, Lewis B, Nelson P, et al. J. Med. Chem., 1969, 13: 203
55. Hafferl W, Hary A. J. Labelled Compounds, 1973, 9(2): 293
56. Fried H, Harrison I T. DE 2 005 454, 1970 (Chem. Abstr., 1970, 74:3436k)
57. Fried H, Harrison I T. US 3 958 012, 1976(Chem. Abstr., 1976, 85:46295z)
58. Fuji K, Node M, Tanaka F, Hosoi S. Tetrahedron Lett., 1989, 30: 2825
59. Dang T P, Kagan H B. J. Chem. Soc., Chem. Commun., 1971, 481
60. Manimaran T, Wu T C, Klobucar W D, et al. Organometallics, 1993, 13:1467
61. Giordano C, Castald G, Uggeri F. Angew. Chem. Int. Ed. Engl., 1984, 23(6):413
62. Castaldi G, Cavicchioli S, Giordano C, et al. J. Org. Chem., 1987, 52: 3018
63. Tsuchihashi G, Mitamura S, Kitajima K, et al. Tetrahedron Lett., 1982, 22: 5427
64. Tsuchihashi G, Kitajima K, Mitamura S. EP 67 698, 1982 (Chem. Abstr., 1982, 98: 178945g)
65. Wilson W H. Chirality, 1994, 6(3): 216
66. (Lu X Y). (Progress in Chemistry), 1998, 10(2): 123
67. (Dai L X), (Lu X Y), (Zhu G M). (Chemistry Bulletin), 1995, 6:15
68. Sheldon R A. Chirotechnology: Industrial Synthesis of Optically Active Compounds. New York: Marcel Dekker, 1993