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1-methyl-3-phenyl-3-thiocyanato-1H,3H-quinoline-2,4-dione: A novel thiocyanating agent

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Title: 1-methyl-3-phenyl-3-thiocyanato-1H,3H-quinoline-2,4-dione: A novel thiocyanating agent
Author: Klásek, Antonín; Mrkvička, Vladimír
Document type: Peer-reviewed article (English)
Source document: Journal of Heterocyclic Chemistry. 2003, vol. 40, issue 5, p. 747-752
ISSN: 0022-152X (Sherpa/RoMEO, JCR)
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DOI: https://doi.org/10.1002/jhet.5570400501
Abstract: Under mild reaction conditions, the thiocyanato group is selectively transferred from 1-methyl-3-phenyl-3-thiocyanato-1H,3H-quinoline-2,4-dione (3) to some nucleophiles. Aliphatic primary and secondary amines are converted to S-cyanothiohydroxylamines, anilines afford p-thiocyanatoanilines, Wittig reagent is thiocyanated in ?-position, and thiols are oxidized to disulfides.
Full text: http://onlinelibrary.wiley.com/doi/10.1002/jhet.5570400501/abstract
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Citace článku v časopise:
KLÁSEK, Antonín a Vladimír MRKVIČKA. 1-methyl-3-phenyl-3-thiocyanato-1H,3H-quinoline-2,4-dione: A novel thiocyanating agent. Journal of Heterocyclic Chemistry [online]. 2003, vol. 40, iss. 5, s. 747-752. [cit. 2024-04-19]. ISSN 0022-152X. Dostupné z: http://onlinelibrary.wiley.com/doi/10.1002/jhet.5570400501/abstract.

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