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Syntheses of Terpenoids having a Medium-membered Ring: Synthetic Study on Taxane-typed Compounds

Research Project

Project/Area Number 60571011
Research Category

Grant-in-Aid for General Scientific Research (C)

Allocation TypeSingle-year Grants
Research Field Chemical pharmacy
Research InstitutionThe Institute of Physical and Chemical Research

Principal Investigator

OHTSUKA Yasuo  The Institute of Physical and Chemical Research, 有機合成化学研究室, 研究員 (40087523)

Co-Investigator(Kenkyū-buntansha) FUKUI Mineo  The Institute of Physical and Chemical Research, 有機合成化学研究室, 研究員 (70109792)
Project Period (FY) 1985 – 1986
Project Status Completed (Fiscal Year 1988)
Budget Amount *help
¥1,800,000 (Direct Cost: ¥1,800,000)
Fiscal Year 1986: ¥300,000 (Direct Cost: ¥300,000)
Fiscal Year 1985: ¥1,500,000 (Direct Cost: ¥1,500,000)
Keywordstaxane / eight-membered ketone / medium-membered ring / X-ray crystallography / configuration / 12-membered lactam sulfoxide / intramolecular cyclization / irone / X線結晶構造解析 / 熱力学的安定性 / 分子模型 / 分子力学 / 中環状ケトン合成法 / 2,6,6-トリメチル-5-ホルミル-1-シクロヘキセンカルボン酸エステル
Research Abstract

The key step involved a novel construction of the eight-membered ring in taxane-typed compounds by a base-induced intramolecular cyclization of 12-membered lactam sulfoxides we developed for the preparation of medium-ring ketones. A cyclohexene moiety corresponding to the A ring was constructed by the Diels-Alder reaction and converted into 12-membered lactam sulfoxide. Intramolecular cyclization of the lactam sulfoxide was proceeded smoothly to give 4,8,11,11-tetramethylbicyclo[5.3.1]undec-8-en-3-one corresponding to the A and B rings. The allyl group introduced stereoselectively at the C-4 position in this ketone was converted into a methoxycarbonylpropyl group and construction of the C ring by reductive coupling with Ti(0) reagent afforded the taxane-typed compound, 8 ,12,15,15-tetramethyltricyclo[9.3.1.0^<3,8>]-pentadec-12-en-4-one, in which the configuration at the C-3 was determined to be (B/C-cis) by X-ray crystallography. MM2 calculation of various taxane-typed compounds suggested that the desired B/C-trans configuration would be obtained by the synthesis of the analogue having a double bond at the C-11,C-12 positions in the same way. Thus, 2,6,6-trimethy1-5-formy1-1-cyclohexenyl-1-carboxylate was synthesized as the starting material through only 3 steps from ethyl acetoacetate. Two conformational isomers of 12-membered lactam sulfides were obtained from the cyclohexene derivative and those structures were confirmed by X-ray crystallography and/or ^1H-NMR. The desired 8-membered ring ketone corresponding to the A and B rings was synthesized from the minor isomer but not from the major one. (+)-and (-)-1,5,5-Trimethyl-4 -hydroxymethyl-6 -benzyloxyethylcyclohexenes, optical active precursors for taxane synthesis, were synthesized and, for determinatiof absolute configuration, converted into (+)- and (-)-irones, naturally occurring perfume, respectively.

Report

(2 results)
  • 1988 Final Research Report Summary
  • 1986 Annual Research Report
  • Research Products

    (6 results)

All Other

All Publications (6 results)

  • [Publications] Y.Ohtsuka.;T.Oishi: Chem.Pharm.Bull.,.

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1988 Final Research Report Summary
  • [Publications] Y.Ohtsuka,;F.Itoh.;T.Oishi: Chem.Pharm.Bull.,.

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1988 Final Research Report Summary
  • [Publications] Y.Ohtsuka,;J.Uzawa.;T.Oishi: Tetrahedron Lett.,.

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1988 Final Research Report Summary
  • [Publications] Y. Ohtsuka; T. Oishi: "Studies on Taxane Synthesis III. Stereocontrolled Synthesis of the Twelve-membered Lactam Sulfoxide as the Precursor of 4,8,12,12-Tetramethyl-3-oxobicyclo[5.3.1]undec-8-ene" Chem. Pharm. Bull.,.

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1988 Final Research Report Summary
  • [Publications] Y. Ohtsuka; F. Itoh; T. Oishi: "Studies on Taxane Synthesis IV. Stereocontrolled Synthesis of Optical Active Cyclohexene Derivatives Corresponding to the A Ring of Taxane Diterpenes. Syntheses of (+)- and (-)-Irones." Chem. Pharm. Bull.,.

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1988 Final Research Report Summary
  • [Publications] Y. Ohtsuka; J. Uzawa; T. Oishi: "Synthesis of the Tricyclic Taxane Ring System" Tetrahedron Lett.,.

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1988 Final Research Report Summary

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Published: 1987-03-31   Modified: 2016-04-21  

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