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Synthesis 1987; 1987(4): 349-353
DOI: 10.1055/s-1987-27940
DOI: 10.1055/s-1987-27940
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© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved.
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or duplication of any kind, translating, preparation of microfilms, and electronic
data processing and storage.Synthesis and Cyclization Reaction of 2-(Hydroxyimino)alkyl N,N-Dialkylthiocarbamates, S-[2-(Hydroxyimino)alkyl] O-Methyl Dithiocarbonate, and Alkyl 2-(Hydroxyimino)alkyl Trithiocarbonates
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Publikationsverlauf
Publikationsdatum:
20. August 2002 (online)
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2-(Hydroxyimino)alkyl dialkyldithiocarbamates and alkyl 2-(hydroxyimino)alkyl trithiocarbonates react with tosyl isocyanate as dehydrating agent to give bis(4-isothiazolyl) disulfides in moderate yields. However, treatment of S-[2-(hydroxyimino)phenylethyl] O-methyl dithiocarbonate with tosyl isocyanate affords a novel heterocycle 3-phenyl-4H-1,5,2-oxathiazine-6-thione, in 49% yield.