Microwave induced novel synthetic route to organomercurials
M Kidwai, Y Goel
Index: Kidwai, Mazaahir; Goel, Yogesh Polyhedron, 1996 , vol. 15, # 17 p. 2819 - 2824
Full Text: HTML
Citation Number: 16
Abstract
Organomercurials of 2-mercapto-5-methyl-1, 3, 4-thiadiazole and 2-mercapto-5-[4′-methyl quinolinyl-2-oxy methyl]-1, 3, 4-oxadiazole with aryl mercuric chloride have been synthesized under microwave irradiation in open vessels in a domestic microwave oven within a few minutes. This reaction rate was ca 100 times faster than the reaction rate in the conventional way. These organomercurials have a 1: 1 stoichiometric ratio of aryl mercury ...
Related Articles:
[D'Ans, J.; Zimmer, H.; Bergmann, H. Chemische Berichte, 1952 , vol. 85, p. 583 - 585]
[Journal of the American Chemical Society, , vol. 82, p. 3887 - 3892]
Iodine-catalyzed one-pot synthesis of 2h-pyrans by domino knoevenagel/6π-electrocylization
[Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, , p. 1211 - 1216 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, , p. 1186 - 1192]
Substituent effects in aromatic substitution of aryltriethyltin compounds by mercuric halides
[Journal of Organometallic Chemistry, , vol. 363, p. 39 - 44]
Journal of the American Pharmaceutical Association (1912–1939)
[Journal of the American Pharmaceutical Association (1912-1977), , vol. 40, p. 95 - 97 Hg: MVol.B2, 101, page 609 - 610 N. S. A., AECU-863 (1950) 1/9 , vol. 4, p. 5209]