Synthesis 2014; 46(04): 496-502
DOI: 10.1055/s-0033-1338575
paper
© Georg Thieme Verlag Stuttgart · New York

Synthesis of 6-Substituted 3-(Alkoxycarbonyl)-5-aryl-α-pyrones

Autoren

  • Takuya Miura

    Kyoto Pharmaceutical University, 1 Misasagi-Shichono, Yamashina, Kyoto 607-8412, Japan   Fax: +81(75)5954775   eMail: yamasita@mb.kyoto-phu.ac.jp
  • Saki Fujioka

    Kyoto Pharmaceutical University, 1 Misasagi-Shichono, Yamashina, Kyoto 607-8412, Japan   Fax: +81(75)5954775   eMail: yamasita@mb.kyoto-phu.ac.jp
  • Naoto Takemura

    Kyoto Pharmaceutical University, 1 Misasagi-Shichono, Yamashina, Kyoto 607-8412, Japan   Fax: +81(75)5954775   eMail: yamasita@mb.kyoto-phu.ac.jp
  • Hiroki Iwasaki

    Kyoto Pharmaceutical University, 1 Misasagi-Shichono, Yamashina, Kyoto 607-8412, Japan   Fax: +81(75)5954775   eMail: yamasita@mb.kyoto-phu.ac.jp
  • Minoru Ozeki

    Kyoto Pharmaceutical University, 1 Misasagi-Shichono, Yamashina, Kyoto 607-8412, Japan   Fax: +81(75)5954775   eMail: yamasita@mb.kyoto-phu.ac.jp
  • Naoto Kojima

    Kyoto Pharmaceutical University, 1 Misasagi-Shichono, Yamashina, Kyoto 607-8412, Japan   Fax: +81(75)5954775   eMail: yamasita@mb.kyoto-phu.ac.jp
  • Masayuki Yamashita*

    Kyoto Pharmaceutical University, 1 Misasagi-Shichono, Yamashina, Kyoto 607-8412, Japan   Fax: +81(75)5954775   eMail: yamasita@mb.kyoto-phu.ac.jp
Weitere Informationen

Publikationsverlauf

Received: 22. Oktober 2013

Accepted after revision: 18. November 2013

Publikationsdatum:
16. Dezember 2013 (online)


Graphical Abstract

Abstract

An efficient synthesis of 6-substituted 3-(alkoxycarbonyl)-5-aryl-α-pyrones is reported. This methodology consists of the successive manipulation of an addition–elimination reaction between benzyl ketone derivatives and dimethyl methoxymethylenemalonate, and an acid-catalyzed condensation reaction. The synthesis is applicable to various 5-p-substituted-aryl 6-substituted α-pyrones and good to excellent yields were obtained over two steps from benzyl ketone derivatives that were easily prepared from phenylacetic acid by the Negishi coupling or the Claisen decarboxylation reaction.

Supporting Information