An efficient and novel synthesis of carbamate esters from the coupling of amines, halides and carbon dioxide in the presence of basic resin

Chinese Chemical Letters

Volumn 17, Issue 10, 2006, Pages 1309-1312

  Chaturvedi, Devdutt ^a   Mishra, Nisha ^b   Mishra, Virendra ^b  

^a CENTRAL DRUG RESEARCH INSTITUTE   (India)

^b BSA College   (India)

Author keywords

Alkyl halides; Amines; Basic resin (Amberlite IRA 400); Carbamates; Carbon dioxide

Indexed keywords

EID: 33751069833     PISSN: 10018417     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (34)

1. (a) S. Ray, D. Chaturvedi, Drugs of the Future, 2004, 29, 343.
2. (b) S. Ray, S. R. Pathak, D. Chaturvedi, Drugs of the Future, 2005, 30, 161.
3. (a) P. Adams, F. A. Baron, Chem. Rev., 1965, 65, 567.
4. (b) A. Mateen, S. Chapalamadugu, et al., Biol. Degrad. Biorem. Toxic. Chem., 1994, 198.
5. (c) Y. Y. Wigfield, Food Sci. Technol. (NY), 1996, 77, 1501.
6. (a) V. Snieckus, Chem. Rev., 1990, 90, 879.
7. (b) W. W. Cleraland, T. S. Andrews, et al., Chem. Rev., 1998, 98, 549.
8. (c) F. Tanaka, Chem. Rev., 2002, 102, 4885.
9. rd ed. John Wiley and Sons, Inc. NY, 1999, 503.
10. (a) J. P. Mayer, G. S. Lewis, et al., Tetrahedron Lett., 1997, 38, 8445.
11. (b) H. P. Buchstaller, Tetrahedron, 1998, 54, 3465.
12. (c) P. T. Holte, L. Thijs, Tetrahedron Lett., 1998, 39, 7404.
13. (a) T. Matsui, T. Kondo, Y. Nishita, et al., Bioorg. Med. Chem. Lett., 2002, 12, 907.
14. (b) T. Seko, M. Kato, H. Kohno, et al., Bioorg. Med. Chem. Lett., 2002, 12, 915.
15. (a) D. P. N. Satchell, R. S. Satchell, Chem. Soc. Rev., 1975, 4, 231.
16. (b) S. Raucher, D. S. Jones, Synth. Commun., 1985, 15, 1025.
17. (a) T. W. Leung, B. D. Domblk, Chem Commun., 1992, 205.
18. (b) T. Mizuno, J. Takahashi, A., Tetrahedron, 2002, 58, 7805.
19. For review article on carbon dioxide in carbamates synthesis, see: (a) D. Chaturvedi, Monatsh. Chem., 2006, 137, 127.
20. (b) D. Chaturvedi, Current Org. Chem., 2006, in press.
21. (a) D. Chaturvedi, A. Kumar, S. Ray, Synth. Commun., 2002, 32, 2651.
22. (b) D. Chaturvedi, A. Kumar, S. Ray, Tetrahedron Lett., 2003, 44, 7637.
23. (c) D. Chaturvedi, S. Ray, Monasth. Chem., 2006, 137, 201.
24. (d) D. Chaturvedi, S. Ray, Tetrahedron Lett., 2006, 47, 1307.
25. (e) D. Chaturvedi, S. Ray, Monatsh. Chem., 2006, 137, 311.
26. (f) D. Chaturvedi, S. Ray, Monatsh. Chem., 2006, 137, 459
27. (g) D. Chaturvedi, S. Ray, Monatsh. Chem., 2006, 137, 465.
28. (h) D. Chaturvedi, S. Ray, Lett. Org. Chem., 2006, 3(in press).
29. D. Chaturvedi, S. Ray, Tetrahedron Lett., 2006, 47 (in press).
30. (a) D. Chaturvedi, S. Ray, Lett. in Org. Chem., 2005, 2, 742.
31. (b) D. Chaturvedi, S. Ray, J. Sulfur Chem., 2005, 26, 365.
32. (c) D. Chaturvedi, S. Ray, J. Sulfur Chem., 2006, 27, 265.
33. D. Chaturvedi, A. Kumar, S. Ray, Indian J. Chem., 2004, 43B, 437.
34. D. Chaturvedi, A. Kumar, R. Rastogi, et al., US Patent, 2004, 192688, CA 141: 2955752.