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Total Synthesis of ent-Ascospiroketal B.
Hara, Yoshiyori; Honda, Tatsuya; Arakawa, Kazuto; Ota, Koichiro; Kamaike, Kazuo; Miyaoka, Hiroaki.
Afiliación
  • Hara Y; School of Pharmacy, Tokyo University of Pharmacy and Life Sciences , 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan.
  • Honda T; School of Pharmacy, Tokyo University of Pharmacy and Life Sciences , 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan.
  • Arakawa K; School of Pharmacy, Tokyo University of Pharmacy and Life Sciences , 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan.
  • Ota K; School of Pharmacy, Tokyo University of Pharmacy and Life Sciences , 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan.
  • Kamaike K; School of Pharmacy, Tokyo University of Pharmacy and Life Sciences , 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan.
  • Miyaoka H; School of Pharmacy, Tokyo University of Pharmacy and Life Sciences , 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan.
J Org Chem ; 83(4): 1976-1987, 2018 02 16.
Article en En | MEDLINE | ID: mdl-29389118
ABSTRACT
Ascospiroketal B was isolated from a marine-derived fungus as a structurally unique polyketide possessing a rare tricyclic core including 5,5-spiroketal-γ-lactone. An asymmetric total synthesis of ent-ascospiroketal B was achieved using an original synthetic route. The synthesis included the stereoselective construction of 5,5-spiroketal for ascospiroketal B and stereocontrolled construction of a quaternary asymmetric carbon by rearrangement of a trisubstituted epoxide.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Compuestos de Espiro / Éteres Cíclicos Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Compuestos de Espiro / Éteres Cíclicos Idioma: En Año: 2018 Tipo del documento: Article