Oxidation of 3-aryl-1H-benzo[f]chromenes with Koser’s reagent – synthesis of benzoflavylium tosylates View Full Text


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Article Info

DATE

2020-05

AUTHORS

Vitaly А. Osyanin, Maxim R. Demidov, Dmitry V. Osipov, Yuri N. Klimochkin

ABSTRACT

The oxidation of 3-aryl-1H-benzo[f]chromenes with Koser’s reagent in methanol afforded a series of benzoflavylium tosylates. This reaction is the first example of the use of polyvalent iodine compounds to access arene-condensed pyrylium salts.

PAGES

603-606

References to SciGraph publications

  • 1983-08. 4H-pyrans (review) in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1007/s10593-020-02705-5

    DOI

    http://dx.doi.org/10.1007/s10593-020-02705-5

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1128161248


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