A new synthesis of 2-substituted-1,3-dithianes from trichloromethyl compounds

Tetrahedron Letters

Volumn 48, Issue 7, 2007, Pages 1201-1204

  Rivera, Nancy González ^a   Becerril, David Corona ^a   Guadarrama Pérez, Carlos ^a   Covarrubias Zuñiga, Adrian ^b   Avila Zárraga, José Gustavo ^b   Romero Ortega, Moisés ^a  

^a UNIVERSIDAD AUTÓNOMA DEL ESTADO DE MÉXICO   (Mexico)

^b UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

Author keywords

1,3 Dithiane derivatives; 1,3 Propapnedithiol; 2 Trichloroacetylpirrole; Trichloromethyl compounds

Indexed keywords

1,3 DITHIANE DERIVATIVE; 1,3 PROPANEDITHIOLATE 1,3 PROPANEDITHIOL DERIVATIVE; CHLOROFORM; THIOL DERIVATIVE; TRICHLOROMETHYL DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; BINDING KINETICS; CHEMICAL REACTION KINETICS; ELECTRON TRANSPORT; SUBSTITUTION REACTION; SYNTHESIS;

EID: 33846251973     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.12.066     Document Type: Article

References (39)

1. Seebach D. Angew. Chem., Int. Ed. Engl. 8 (1969) 639
2. Grobel B.T., and Seebach D. Synthesis (1977) 357
3. Bulman Page O.C., Van Niel M.B., and Prodger J.C. Tetrahedron 45 (1989) 7643
4. Greene T.W., and Wuts P.G.M. Protective Groups in Organic Synthesis. 2nd ed. (1991), Wiley, New York pp 178-207
5. Corey E.J., and Seebach D. J. Org. Chem. 31 (1966) 4097
6. Eliel E.L., and Morris-Natschke. J. Am. Chem. Soc. 106 (1984) 2937
7. Corey E.J., and Seebach D. J. Org. Chem. 40 (1975) 231
8. Corey E.J., and Seebach D. Angew. Chem., Int. Ed. Engl. 4 (1965) 1075 1077
9. Garlaschelli L., and Vidari G. Tetrahedron Lett. 31 (1990) 5815
10. Hauptmann H., and Campos M.M. J. Am. Chem. Soc. 72 (1950) 5815
11. Seebach D., and Kolb M. Chem. Ind. (London) (1974) 687
12. Ong B.S. Tetrahedron Lett. (1980) 4225
13. Kumar V., and Dev S. Tetrahedron Lett. 24 (1983) 1289
14. Ku B., and Oh D.Y. Synth. Commun. 19 (1989) 433
15. Ong B.S., and Chan T.H. Synth. Commun. 7 (1977) 283
16. Corey E.J., and Simoji K. Tetrahedron Lett. 24 (1983) 169
17. Komatsu N., Uda M., and Suzuki H. Synlett (1995) 984
18. Choudray B.M., and Sudha Y. Synth. Commun. (1996) 2993
19. Djerassi C., and Gorman M. J. Am. Chem. Soc. 75 (1953) 3704
20. Wilson Jr. G.E., Huang M.G., and Schloman W.W. J. Org. Chem. 33 (1968) 21343
21. Evans D.A., Truesdale L.K., Grimm K.G., and Nesbit S.L. J. Am. Chem. Soc. 99 (1977) 5009
22. Pantey H.K., and Margan S. Tetrahedron Lett. 37 (1996) 4621
23. Yadav J.S., Reddy B.S., and Pandey S.K. Synlett (2001) 238
24. Yadav J.S., Reddy B.S., and Pandey S.K. Synth. Commun. 32 (2002) 715
25. Kamal A., and Chouhan G. Synlett (2002) 474
26. Firouzabadi H., Iranpoor H., and Hazarkhani H. J. Org. Chem. 66 (2001) 7527
27. Kanta D.S. Tetrahedron Lett. 45 (2004) 2339
28. Tetrahedron Lett. 45 (2004) 7719
29. Capito E., Bernardi L., Comes-Franchini M., Fini F., Fochi M., Polliano S., and Ricci A. Tetrahedron: Asymmetry 16 (2005) 3232
30. Seebach D. Synthesis 1 (1969) 17
31. Corey E.J., and Erickson B.W. J. Org. Chem. 36 (1971) 3553
32. Smith A.B., and Adams C.M. Acc. Chem. Res. 37 (2004) 365
33. Hagooly A., Sasson R., and Rozen S. J. Org. Chem. 68 (2003) 8287
34. Takeda T., Kuroi S., Ozaki M., and Tsubouchi A. Org. Lett. 6 (2004) 3207
35. Romero-Ortega M., Fuentes A., González C., Morales D., and Cruz R. Synthesis (1999) 225
36. Romero-Ortega M., Reyes H., Covarrubias-Zúñiga A., Cruz R., and Avila-Zarraga J.G. Synthesis (2003) 2765
37. Guzmán A., Romero M., Talamás F.X., Villena R., Greenhouse R., and Muchowski J.M. J. Org. Chem. 61 (1996) 2470
38. 8
39. +, 12), 209 (100).