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Efficient Enantioselective Synthesis of Oxahelicenes Using Redox/Acid Cooperative Catalysts.
Sako, Makoto; Takeuchi, Yoshiki; Tsujihara, Tetsuya; Kodera, Junpei; Kawano, Tomikazu; Takizawa, Shinobu; Sasai, Hiroaki.
Afiliación
  • Sako M; The Institute of Scientific and Industrial Research (ISIR), Osaka University , Mihogaoka, Ibaraki-shi, Osaka 567-0047, Japan.
  • Takeuchi Y; The Institute of Scientific and Industrial Research (ISIR), Osaka University , Mihogaoka, Ibaraki-shi, Osaka 567-0047, Japan.
  • Tsujihara T; Department of Medicinal and Organic Chemistry, School of Pharmacy, Iwate Medical University , Yahaba, Iwate 028-3694, Japan.
  • Kodera J; The Institute of Scientific and Industrial Research (ISIR), Osaka University , Mihogaoka, Ibaraki-shi, Osaka 567-0047, Japan.
  • Kawano T; Department of Medicinal and Organic Chemistry, School of Pharmacy, Iwate Medical University , Yahaba, Iwate 028-3694, Japan.
  • Takizawa S; The Institute of Scientific and Industrial Research (ISIR), Osaka University , Mihogaoka, Ibaraki-shi, Osaka 567-0047, Japan.
  • Sasai H; The Institute of Scientific and Industrial Research (ISIR), Osaka University , Mihogaoka, Ibaraki-shi, Osaka 567-0047, Japan.
J Am Chem Soc ; 138(36): 11481-4, 2016 09 14.
Article en En | MEDLINE | ID: mdl-27574874
ABSTRACT
An efficient and enantioselective synthesis of oxa[9]helicenes has been established via vanadium(V)-catalyzed oxidative coupling/intramolecular cyclization of polycyclic phenols. A newly developed vanadium complex cooperatively functions as both a redox and Lewis acid catalyst to promote the present sequential reaction and afford oxa[9]helicenes in good yields with up to 94% ee.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2016 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2016 Tipo del documento: Article País de afiliación: Japón