Microwave assisted synthesis of novel organomercurials in 'dry media'

Polyhedron

Volumn 18, Issue 20, 1999, Pages 2641-2643

  Kidwai, Mazaahir ^a   Misra, Preeti ^a   Bhushan, Kumar Ranjan ^a  

^a UNIVERSITY OF DELHI   (India)

Author keywords

Dry media; Heterocycle; Microwave assisted; Organomercurials; Solid support

Indexed keywords

CHLORINE COMPOUNDS; MERCURY COMPOUNDS;

'DRY' [; BARBITURIC ACID; BENZOQUINONES; DRY MEDIUM; HETEROCYCLES; MICROWAVE ASSISTED SYNTHESIS; MICROWAVE-ASSISTED; ORGANOMERCURIALS; SOLID SUPPORTS; THIOBARBITURIC ACID;

MICROWAVE IRRADIATION;

EID: 0001663488     PISSN: 02775387     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0277-5387(99)00159-X     Document Type: Article

References (28)

1. Kaur J., Marwaha S., Boyd M.R., Sodhi G.S. Neoplasma. 42:1995;191.
2. Baijal G., Day A.N. J. Indian Chem. Soc. 52:1975;657.
3. Santucci B., Cannistraci C., Cristaudo A., Camera E., Picardo M. Contact Dermatitis. 38:1998;325.
4. Goto T., Hayakawa H., Watanabe Y., Yanaji A. Eur. Pat. Appl. 1993, EP 572855. Chem. Abstr. 120:1994;164200.
5. Allksanian M.V., Kramer M.S., Agababian R.V., Yu, Zakharian Z.T., Mnjoyan S.L., Martirosian A.D. Khim. Farm. Zh. 28:1994;33.
6. Allksanian M.V., Kramer M.S., Agababian R.V., Yu, Zakharian Z.T., Mnjoyan S.L., Martirosian A.D. Chem. Abstr. 122:1995;55764.
7. Kano S., Naguchi T. Jap. Pat. 1967, 13948. Chem. Abstr. 68:1968;39820.
8. Modi B.R., Mistry B.D., Desai K.R. Orient. J. Chem. 9:1993;369.
9. Colinas J.R., Burkart P.T., Lawrence D.A. Toxicol. Appl. Pharmacol. 29:1994;95.
10. Nishina A., Ito M. Jpn. Kokai Tokkyo Koho JP 02, 202, 804. Chem. Abstr. 114:1991;22693.
11. Bogatskij V.A., Andronati S.A., Litvinova L.A., Seboleva S.G., Denisenko P.P., Shamaryan M.I., Polyakova M.A., Silivra V.A. Izobreteniya. 37-38:1993;233.
12. Larock R.C., Lu Y.D. Tet. Lett. 29:1998;6761.
13. Deacon G.B., Stretton G.N. Aust. J. Chem. 38:1985;419.
14. El-Sawi E., El-Shahat M.F., Moti F.A., El-Messary S. J. Chem. Soc. Pak. 6:1984;77.
15. J. Thurey, Les Microondes et Leurs Effects sur la Matiere; Technique et Documentation, Cavoisier, Paris, 1989.
16. Caddick S. Tetrahedron. 51:1995;10403.
17. M. Kidwai, P. Misra, Synth. Commun. (in press).
18. Kidwai M., Kumar R. Gazz. Chem. Ital. 127:1997;263.
19. Gedye R.N., Smith F.E., Westway K.C., Ali H., Baldisera L., Laberge L., Rowell J. Tetrahedron Lett. 26:1986;279.
20. D.C. Dittmer, Chem. Ind. (1997) 779.
21. Kidwai M., Misra P., Kumar R., Saxena R.K., Gupta R., Bradoo S. Monatsh. Chem. 128:1998;1291.
22. Kidwai M., Kumar R., Goel Y. Main Gp. Met. Chem. 20:1997;367.
23. M. Kidwai, P. Kumar, J. Chem. Res. (s) (1997) 178.
24. Nitravati I., Dass D., Dutt S. Proc. Indian Acad. Sci. 8A:1938;145.
25. Kidwai M., Goel Y. Polyhedron. 15:1996;2819.
26. Aluminium oxide, Basic, Brockmann I (Aldrich Chem. Co., Cat. No. 19, 944-3, ~150 mesh, 58A, Surface area 155 m2/g) were used as received.
27. Bram G., Loupy A., Majdoub M., Gutierrez E., Ruiz-Hitzky E. Tetrahedron. 46:1990;5167.
28. Bram G., Decodts G. Tetrahedron Lett. 21:1980;5011.