Journal
CHEMICAL COMMUNICATIONS
Volume 46, Issue 5, Pages 797-799Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b915294f
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Thiosilane and a catalytic amount of a Bronsted acid mediate the novel domino-type rearrangement reaction of the 4,4-disubstituted cyclohexadienones to produce the 3,4-disubstituted benzenethioethers; the key step is 1,2-addition of thiosilane to dienone.
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