Oxidation of dithiocarbamates and synthesis of a stable sulfine

Tetrahedron Letters

Volumn 39, Issue 49, 1998, Pages 8983-8986

  Chevrie, David ^a   Metzner, Patrick ^a  

^a UNIVERSITÉ DE CAEN   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DITHIOCARBAMIC ACID; FUNGICIDE; SULFOXIDE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CRYSTAL STRUCTURE; OXIDATION; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 0032481087     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)02033-4     Document Type: Article

References (25)

1. 1. Thiocarbamates Pesticides - Ethylenthiourea - and Propylenthiourea: General Introduction; World Health Organization: Geneva, 1988.
2. 2. Cremlyn, R. J. Agrochemicals. Preparation and Mode of Action; John Wiley: Chichester, 1991.
3. 3. Worthing, C. R.; Walker, S. B. The Pesticide Manual; British Crop Protection Council: Thorton Heath (UK), 1987.
4. 4. Damani, L. A. Sulphur-Containing Drugs and Related Compounds - Chemistry Biochemistry and Toxicology. Metabolism of Sulphur Functional Groups; Ellis Horwood: Chichester, 1989; Vol. 1, Part B.
5. 5. Madan, A.; Faiman, M. D. Drug Metab. Disp. 1994, 22, 324-330.
6. 6. Madan, A.; Williams, T. D.; Faiman, M. D. Mol. Pharmacol. 1994, 46, 1217-1225.
7. 7. Hart, B. W.; Faiman, M. D. Biochem. Parmacol. 1992, 43, 403-406.
8. 8. Madan, A.; Faiman, M. D. J. Pharmacol. Exp. Ther. 1995, 272, 775-780.
9. 9. Schupan, I.; Segall, Y.; Rosen, J. D.; Casida, J. E. Sulfur in Pesticide Action and Metabolism; Rosen, J. D.; Magee, P. S.; Casida, J. E. Ed.; American Chemical Society: Washington, 1981, pp 65-82.
10. 10. Pedras, M. S. C.; Taylor, J. L. J. Org. Chem. 1991, 56, 2619-2621.
11. 11. Pedras, M. S. C.; Taylor, J. L. J. Nat. Prod. 1993, 56, 731-738.
12. 12. Pedras, M. S. C.; Okanga, F. I. J. Org. Chem. 1998, 63, 416-417.
13. 13. Walter, W.; Bode, K.-D. Liebigs Ann. Chem. 1966, 692, 108-118.
14. 14. Segall, Y.; Casida, J. E. J. Agric. Food Chem. 1983, 31, 242-246.
15. 15. Watanabe, Y.; Ishimura, Y. J. Org. Chem. 1988, 53, 2119-2120.
16. 16. Hanefeld, W.; Schlitzer, M.; Schütz, H.; Wocaldo, S.; Massa, W. Liebigs Ann. Chem. 1992, 325-336.
17. 17. Walter, W.; Bode, K.-D. Liebigs Ann. Chem. 1965, 681, 64-84.
18. 18. Zwanenburg, B. Recl. Trav. Chim. Pays-Bas 1982, 101, 1-27.
19. 19. Zwanenburg, B.; Thijs, L.; Strating, J. Recl. Trav. Chim. Pays-Bas 1971, 90, 614-629.
20. 20. Carlsen, L.; Holm, A.; Koch, E.; Stilkerieg, B. Acta Chem. Scand., Ser. B 1977, 31, 679-682.
21. 21. Adam, W.; Deeg, O.; Weinkötz, S. J. Org. Chem. 1997, 62, 7084-7085.
22. 22. Walter, W.; Bode, K.-D. Angew. Chem. 1963, 75, 208.
23. 23. Davis, F. A.; Billmers, R. L. J. Am. Chem. Soc. 1981, 103, 7016-7018.
24. 24. Okazaki, R. Organosulfur Chemistry - Synthetic Aspects; Page, P. C. B. Ed.; Academic Press: London, 1995, pp 225-258.
25. 25. Atomic coordinates, bond lengths and angles have been deposited at the Cambridge Crystallographic Data Centre under number 103111. Copies of the data can be obtained free of charge on application to The Director, CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (fax: Int. code +(1223) 336-033; e-mail: teched@ccdc.cam.ac.uk).