Advances in the synthesis of thiocarbamates

Progress in Chemistry

Volumn 20, Issue 7-8, 2008, Pages 1102-1107

  Zhang, Xiaapeng ^a,b   Jing, Huarvshi ^a   Miao, Jianghuan ^a   Lu, Shiwei ^b  

^a HENAN NORMAL UNIVERSITY   (China)

^b DALIAN INSTITUTE OF CHEMICAL PHYSICS   (China)

Author keywords

Carbonylation; Selenium catalyst; Thiocarbamates

Indexed keywords

EID: 50349088721     PISSN: 1005281X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (71)

1. Wood T F, Gardner J H. J. Am. Chem. Soc., 1941, 63: 2741-2742
2. Ryder N S, Frank I, Dupont M C. Antimicrob. Agents Chemother., 1986, 29: 858-860
3. Tatsuya M, Yoshinori N. Biseibutsu, 1988, 4: 36-43
4. Beji M, Sbihi H, Baklouti A, Cambon A. J. Fluorine Chem., 1999, 99: 17-24
5. Oku Y, Sakuma K, Yokoyama K, Miyaji M. Nippon Ishinkin Gakkai Zasshi, 2002, 43: 181-187
6. Goel A, Mazur S J, Fattah R J, Hartman T L, Turpin J A, Huang M, Rice W G, Appella E, Inman J K. Bioorg. Med. Chem. Lett., 2002, 12: 767-770
7. Xue M, Long B H, Fairchild C , Johnston K, Rose W C , Kadow J F, Vyas D M, Chen S H. Bioorg. Med. Chem. Lett., 2000, 10: 1327-1331
8. Hahn H G, Rhee H K, Lee C K, Whang K J. Korean J. Med. Chem., 2000, 10: 66-75
9. Harwood J L. Biochem. Soc. Trans., 1994, 22: 621-624
10. Quistad G B, Sparks S E, Casida J E. Life Sci., 1994, 55: 1537-1544
11. Hart B W, Faiman M D. Biochem. Pharmacol., 1995, 49: 157-163
12. Khan T H, Eno-Amooquaye E A, Searle F, Browne P J, Osbom H M I, Burke P J. J. Med. Chem., 1999, 42: 951-956
13. Li-Pan Z S, Joshi H V, Digenis G A. J. Enzyme Inhib., 1999, 15: 63-77
14. Rodis N P, Digenis G A. J. Enzyme Inhib., 2001, 16: 95-105
15. Nathan R M, Peter C J. J. Med. Chem., 2003, 46: 1066-1080
16. Kochansky J, Cohen C F. J. Agric. Entomol., 1990, 7: 293-304
17. The Pesticide Manual, 9th ed. (ed. Worthing C R). London: British Crop Protection Council, 1991
18. Breiter W A, Baker J M, Koskinen W C. J. Agric. Food Chem., 1998, 46: 1624-1629
19. Lee S J, Caboni P, Tomizawa M, Casida J E. J. Agric. Food Chem., 2004, 52: 95-98
20. Chen Y S, Schuphan I, Casida J E. J. Agric. Food Chem., 1979, 27: 709-712
21. Chen-Hsien W. Synthesis, 1981, 8: 622-623
22. Sanders H J. Chemical & Engineering News, 1981, 59: 20-35
23. Nagao Y, Abe Y, Misono T, Ichizen N, Shima Y, Iesaka H, Furushima M. Nippon Kagaku Kaishi, 1993, 719-727
24. Vidal A, Dinya Z, Mogyorodi F, Mogyorodi F. Applied Catalysis B: Environmental, 1999, 21: 259-267
25. Mizuno T, Junko T, Ogawa A. Tetrahedron, 2003, 59: 1327-1331
26. Sitzmann M E, Gilligan W H. J. Org. Chem., 1985, 50: 5879-5881
27. Johnson D E, DeLane J C, Wisted E E. J. Org. Chem., 1987, 52: 3688-3690
28. Francis B, Victor S. Synthesis, 1992, 1/2: 112-118
29. Marr F, Froehlich R, Hoppe D. Org. Lett., 1999, 1: 2081-2083
30. Procter D J. J. Chem. Soc. Perkin Trans, 1, 2001, 1: 335-354
31. Yuck K O, Jie E P, Dae D S, Ikchoon L. J. Org. Chem., 2004, 69: 3150-3153
32. Bowden S A, Burke J N, Gray F, McKown S, Moseley J D, Moss W O, Murray P M, Welham M J, Young M J. Org. Process Res. Dev., 2004, 8: 33-44
33. Werner E A. J. Chem. Soc., 1890, 57: 283-304
34. Riemschneider R. J. Am. Chem. Soc., 1956, 78: 844-847
35. Klimochkin Y N, Moiseev I K. Zh. Org. Khim., 1987, 23: 2026-2026
36. Arkhipova A V, Malkova K V, Sokolova T N, et al. Russian J. Appl. Chem., 2007, 80: 162-163
37. Edwards J D, Pianka M. J. Chem. Soc., 1965, 12: 7338-7344
38. Kwart H, Evans E R. J. Org. Chem., 1966, 31: 410-413
39. Newman M S, Karnes H A. J. Org. Chem., 1966, 31: 3980-3984
40. Kashinath T S, Hiralal N R, Srinivasachari R. IN 175790 A, 1995
41. Jonathan D M, Philip L. Tetrahedron, 2007, 63: 4120-4125
42. Jonathan D M, Rosalind F S, Olivier N T, et al. Tetrahedron, 2006, 62: 4685-4689
43. Hackler R E, Balko T W. J. Org. Chem., 1973, 38: 2106-2109
44. Sakamoto M, Yoshiaki M, Takahashi M, Fujita T, Watanabe S. J. Chem. Soc. Perkin Trans, 1, 1995, 4: 373-377
45. Harayama H, Nagahama T, Kozera T, Kimura M, Fugami K, Tanaka S, Tamaru Y. Bull. Chem. Soc. Jpn., 1997, 70: 445-446
46. Bohme A, Gais H J. Tetrahedron: Asymmetry, 1999, 10: 2511-2514
47. Hans J G, Achim B. J. Org. Chem., 2002, 67: 1153-1161
48. Dyer E, Glenn J F. J. Am. Chem. Soc., 1957, 79: 366-369
49. Tucker H U B, Sayigh A A R. J. Org. Chem., 1967, 32: 3938-3941
50. Ricci A, Danieli R, Pirazzini G. J. Chem. Soc. Perkin Trans. 1, 1977, 9: 1069-1073
51. Weijlard J, Tishler T. J. Am. Chem. Soc., 1951, 73: 1497-1500
52. Evans T W, Dehn W M. J. Am. Chem. Soc., 1930, 52: 3645-3647
53. Tilles H. J. Am. Chem. Soc., 1959, 81: 714-727
54. Hiskey R G, Carroll F I, Smith R F, Corbett R T. J. Org. Chem., 1961, 26: 4756-4757
55. Crosby D G, Niemann C. J. Am. Chem. Soc., 1954, 76: 4458-4463
56. Grzyb J A, Shen M, Yoshina-Ishii C, et al. Tetrahedron, 2005, 61: 7153-7175
57. Mizuno T, Iwai T, Ogawa A, Ito T. Tetrahedron, 2004, 60: 2869-2873
58. Toshiyuki I, Yoshio I. Tetrahedron, 2005, 61: 9157-9163
59. Mizuno T, Nishiguchi I, Okushi T, Hirashima T. Tetrahedron Lett., 1991, 32: 6867-6868
60. Mizuno T, Daigaku T, Nishiguchi I. Tetrahedron Lett., 1995, 36: 1533-1536
61. Jones W D, Reynolds K A, Sperry C K, Lachicotte R J, Godleski S A, Valente R R. Organometallics, 2000, 19: 1661-1669
62. Yutaka N, Hiroaki K. J. Org. Chem., 2005, 70: 2551-2554
63. Jacob J, Reynolds K A, Jones W D, Godleski S A, Valente R R. Organometallics, 2001, 20: 1028-1031
64. Sonoda N, Yasuhara T, Kondo K, Ikeda T, Tsutsumi S. J. Am. Chem. Soc., 1971, 93: 6344-6344
65. Sonoda N, Mizuno T, Murakami S, Konda K, Ogawa A, Ryu I. Angew. Chem. Int. Ed. Engl., 1989, 28: 452-453
66. Mizuno T, Nishiguchi I, Sonoda N. Tetrahedron, 1994, 50: 5669-5680
67. Paolo K. Tetrahedron Lett., 1975, 16: 2087-2088
68. Zhang X P, Lu S W. Synth. Commun., 2007, 37: 3291-3298
69. Zhang X P, Lu S W. Synlett, 2005, 10: 1535-1538
70. Mei J T, Lu S W Chinese J. Catal., 2002, 23: 1-2
71. Mei J T, Yang Y, Xue Y, Lu S W. J. Mol. Catal. A: Chem., 2003, 191: 135-139