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

Klásek, Antonín; Mrkvička, Vladimír

Název:

Autor:

Klásek, Antonín; Mrkvička, Vladimír

Typ dokumentu:

Recenzovaný odborný článek (English)

Zdrojový dok.:

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

Abstrakt:

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.

Plný 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. 2024-04-24]. ISSN 0022-152X. Dostupné z: http://onlinelibrary.wiley.com/doi/10.1002/jhet.5570400501/abstract.

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