Reaction of arylboronic acids with 5-aryl-3-substituted-2-thioxoimidazolin-4-ones
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Add time:09/30/2019 Source:sciencedirect.com
A convenient and efficient catalytic procedure for the selective S-arylation of 2-thioxoimidazolidin-4-ones to give novel S-aryl substituted 2-thiohydantoins under mild reaction conditions using arylboronic acids is described. The anticancer activity of the compounds were evaluated in vitro.
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