Microwave induced novel synthetic route to organomercurials
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 and thiadiazole or oxadiazole moiety. Copyright
Kidwai, Mazaahir,Goel, Yogesh
p. 2819 - 2824
(2008/10/09)
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