A new reagent for the efficient synthesis of disulfides from alkyl halides

Tetrahedron Letters

Volumn 44, Issue 5, 2003, Pages 887-889

  Polshettiwar, Vivek ^a   Nivsarkar, Manisha ^a   Acharya, Jyotiranjan ^a   Kaushik, M P ^a  

^a Process Technology Development Division   (India)

Author keywords

Alkyl halide; Disulfide; Sulfur transfer reagent

Indexed keywords

ALKYL GROUP; BENZYLTRIETHYLAMMONIUM TETRACOSATHIOHEPTAMOLYBDATE; DISULFIDE; HALIDE; MOLYBDIC ACID; REAGENT; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; SYNTHESIS; ULTRAVIOLET RADIATION;

EID: 0037467860     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)02776-4     Document Type: Article

References (36)

1. Organic Sulfur Chemistry: Structure and Mechanism; Oae, S., Ed.; CRC Press: Boca Raton, FL, 1991.
2. Cremlyn R.J. An Introduction to Organo-sulfur Chemistry. 1996;Wiley & Sons, New York.
3. Dhar D.N., Bag A.K. Ind. J. Chem. 23B:1984;974.
4. Firouzbadi H., Iranpoor N., Parham H.A. Synth. Commun. 14:1984;717.
5. Xan J., Wilson E.A., Robert L.D., Norton N.H. J. Am. Chem. Soc. 63:1941;1139.
6. Liu K.-T., Tong Y.C. Synthesis. 1978;669.
7. Schaeffer J.R., Goodhye G.T., Risley H.A., Stevens R.E. J. Org. Chem. 32:1967;392.
8. Drabwicz J., Mikolajczyk M. Synthesis. 1980;32.
9. Iranpoor N., Zeynizadeh B. Synthesis. 1999;49.
10. Abele E., Abele R., Lukevics E. J. Chem. Res. 1999;624.
11. Ali M.H., McDermott M. Tetrahedron Lett. 43:2002;6271.
12. Wallace T.J. J. Org. Chem. 31:1966;1217.
13. Hirano M., Yakabe S., Chikamori H., Clark J.H., Morimoto T. J. Chem. Res. 1998;310.
14. Sanz R., Aguado R., Pedrosa M.R., Arnaiz J.F. Synthesis. 2002;856.
15. Huang X., Chan C.-C. Synthesis. 1982;1091.
16. McKillop A., Kuyuncu D. Tetrahedron Lett. 31:1990;5007.
17. Noureldin M.C., Hendry J., Lee D.G. Synthesis. 1998;1587.
18. Hajipour A.R., Mallakpour S.E. J. Chem. Res. 2000;32.
19. Brandsma L., Wijers H. Recl. Trav. Chim. Pays-Bas. 82:1963;68.
20. Christian J.E., Jenkins G.L., Keagle L.C., Crum J.A. J. Am. Pharm. Assoc. 35:1946;328.
21. Kutil B., Cuda J., Kempny L. Chem. Abstr. 97:1982;72064z.
22. Stiefel E.I. Prog. Inorg. Chem. 22:1973;1.
23. Massoth F.E. Adv. Catal. 27:1978;265.
24. Miller K.F., Bruce A.E., Corbin J.L., Wherland S., Stiefel E.I. J. Am. Chem. Soc. 102:1980;5104. and references cited therein.
25. Rakowski Dubois M., DuBois D.L., Van Derveer M.C., Haltiwanger R.C. Inorg. Chem. 20:1981;3064.
26. Muller A., Reinsch U. Angew. Chem., Int. Ed. Engl. 19:1980;72.
27. Keck H., Kuchen W., Mathow J., Mayer B., Mootz D., Wunderlich H. Angew. Chem., Int. Ed. Engl. 20:1981;975.
28. Simhon E.D., Baenziger N.C., Kanatzidis M., Draganjac M., Coucouvanis D. J. Am. Chem. Soc. 103:1981;1218.
29. Clegg W., Mohan N., Muller A., Neumann A., Rittner W., Sheldrick G.M. Inorg. Chem. 19:1980;2066.
30. Clegg W., Christou G., Garner C.D., Sheldrick G.M. Inorg. Chem. 20:1981;1562.
31. Muller A., Nolte W.O., Krebs B. Inorg. Chem. 19:1978;2835. and references cited therein.
32. Coucouvanis D. Acc. Chem. Res. 14:1981;201. and references cited therein.
33. Halbert T.R., Pan W.H., Stiefel E. J. Am. Chem. Soc. 105:1983;5476.
34. Harpp D.N., MacDonald J.G. Tetrahedron Lett. 25:1984;703.
35. Dhar P., Chandrasekaran S. J. Org. Chem. 54:1989;2998.
36. Ramesha A.R., Chandrasekaran S. Synth. Commun. 22:1992;3277.