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1990 Fiscal Year Final Research Report Summary

Synthetic Studies on the Gelsemium Alkaloids Based on the Biogenetic Speculation

Research Project

Project/Area Number 01470136
Research Category

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

Allocation TypeSingle-year Grants
Research Field Chemical pharmacy
Research InstitutionChiba University

Principal Investigator

SAKAI Shin-ichiro  Chiba University. Department : Fac. Pharm. Sic. Title of Position : Professor, 薬学部, 教授 (20009161)

Co-Investigator(Kenkyū-buntansha) TAKAYAMA Hiromitsu  Chiba University. Department : Fac. Pharm. Sci. Title of Position : Research Ass, 薬学部, 助手 (90171561)
Project Period (FY) 1989 – 1990
KeywordsGelsemium / Indole Alkaloids / Biomimetic Synthesis
Research Abstract

The genus Gelsemium contains more than forty of indole and oxindole alkaloids having various skeletal type. These alkaloids can be classified into five category based on the structural features and on the biogenetic speculation proposed by by us. Throughout the research project, We succeeded in the biomimetic synthesis of four different type of Gelsemium alkaloids.
1. Sarpagine-type indole alkaloids : We succeeded in the synthesis of new Gelsemium alkaloids, koumidine and 19Z-anhydrovobasinediol, starting from ajmaline, which was corresponding chemically to the hypothetical biogenetic intermediate. The configuration of the ethylidene side chain in these alkaloids were also confirmed.
2. Humantenine-type oxindole alkaloids : By the stereoselective transformation of 19Z-anhydrovobasinediol and gardnerine derivative using OsO_4 oxidation, the synthesis of N_a-desmethoxyrankinidine and N_a-desmethoxyhumantenirine, respectively, were accomplished. The absolute configuration of the humantenine … More -type alkaloids was first elucidated by this chemical correlation.
3. Gelsedine-type oxindole alkaloids : Gelsedine-type compounds features the lack of C-21 carbon from usual monoterpenoid indole alkaloids. We first prepared hypothetical biogenetic intermediates, D-norsarpagine compounds from ajmaline and attempted their transformation into the oxindole derivatives. But, thus obtained oxindole had the opposite configuration at C7 spiro-position. Then, along to the alternative biogenetic speculation, we synthesized N_a-desmethoxygelsemicine by the removal of C-21 carbon from humantenine-type type oxindole alkaloids.
4. Koumine : Koumine would generate biogenetically by the bond connection between the C7 adn C20 in the sarpagine-type indole alkaloid. We proved chemically this hypothesis by the palladium-catalyzed intramolecular coupling reaction between the C7 and C20 in 18-acetoxyanhydrovobasinediol.
In conclusion, we succeeded in the synthesis of sarpagine-type, humantenine-type, gelsedine-type, and koumine along to our biogenetic proposal. The synthesis of one of the principal Gelsemium alkaloids, gelsemine, and development of the general procedure for the synthesis of N_a-methoxy oxindole derivatives still remain. Less

  • Research Products

    (22 results)

All Other

All Publications (22 results)

  • [Publications] H.Takayama: "A Biomimimetic Construction of Humantenine Skeleton." Tetrhedron. 45. 1327-1336 (1989)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] H.Takayama: "Partial Synthesis and the Absolute Configuration of Two New Gelsemium Alkaloids,Koumidine and 19ZーTaberpsychine." J.Chem.Soc.,Perkin Trans.I. 1075-1076 (1989)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] H.Takayama: "Chemical Converion of Gardnerine into Koumidine by Inverting the Ethylidene Side Chain with Pd Catalyst." Chem.Pharm.Bull. 37. 2256-2257 (1989)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] H.Takayma: "Biomimetic Synthesis of Koumine by the PalladiumCatalyzed Intramolecular Coupling Reaction of 18ーHydroxytaberpsychine." Heterocycles. 30. 325-327 (1990)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] H.Takayama: "Synthetic Studies on Gelsedine AlkaloidsーI:Stereoselective Preparation of Hypothetical Biogenetic Intermediates,DーNorsarpagine Type Compounds from Ajmaline." Tetrahedron Letters. 31. 1287-1290 (1990)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] H.TaKayama: "Synthetic Studies on Gelsedine AlkaloidsーII:First Construction of Gelsedine Skeleton (Na-Demethoxygelsemicine) from Gardnerine Based on the Alternative Biogenetic Speculation" Tetrahedron Letters. 31. 5483-5486 (1990)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 高山廣光: "ゲルセミウム属アルカロイドの合成研究" 有機合成化学協会誌. 48. 876-890 (1990)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] H.Takayama: "An Efficient Synthetic Pathway to Type Indole Alkaloids、Talcarpine and Alstonerine from Ajmaline." Tetrahedron Letters. 47. 1383-1392 (1991)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] M.Kitajima: "The Steroselective Transformation of Ajmalineto Three Minor Gelsemium Alkaloids,Koumidine,19ZーAnhydrovobasinedior and NーDesmethoxyrankinidine and Their Absolute Configuration."

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] S.Sakai: "Natural products of Woody plants" Springer-verlag, 58 (1989)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] N.Aimi: "The Alkaloids" Acadmic press, 68 (1989)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] H. Takayama,: "A Biomimetic Construction of Humantenine Skeleton." Tetrahedron,. 45. 1327-1336 (1989)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] H. Takayama,: "Partial Synthesis and the Absolute Configuration of Two New Gelsemium Alkaloids, Koumidine and 19Z-Taberpsychine." J. Chem. Soc. Perkin Trans I,. 1075-1076 (1989)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] H. Takayama,: "Chemical Conversion of Gardnerine into Koumidine by Inverting the Ethylidene Side Chain with Pd Catalyst." Chem. Pharm. Bull.,. 37. 2256-2257 (1989)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] H. Takayama,: "Biomimetic Synthesis of Koumine by the Pd Catalyzed Intramolecular Coupling Reaction of 18-Hydroxytaberpsychine." Heterocycles,. 30. 325-327 (1990)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] H. Takayama,: "Synthetic Studies on Gelsedine Alkaloids-I : Stereoselective Preparation of Hypothetical Biogenetic Intermediates, D-Norsarp-agine Type Compounds from Ajmaline." Tetrahedron Letters,. 31. 1287-1290 (1990)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] H. Takayama,: "Synthetic Studies on Gelsedine Alkaloids-II : First Construction of Gelsedine Skeleton (N-Desmethoxygelsemicine) from Gardne-rine Based on the Alternative Biogenetic Speculation." Tetrahedron Letters,. 31. 5483-5486 (1990)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] H. Takayama: "Synthetic Studies on the Gelsemium Alkaloids." J. Synthetic Org. Chem. (Jpn). 48. 876-890 (1990)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] H. Takayama,: "An Efficient Synthetic Pathway to the Macroline-Type Indole Alkaloids, Talcarpine and Alstonerine from Ajmaline." Tetrahedron,. 47. 1383-1392 (1991)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] M. Kitajima,: "The Stereoselective Transformation of Ajmaline into Three Minor Gelsemium Alkaloids, Koumidine, 19Z-Anhydrovobasinediol, and N-Desmethoxyrankinidine and Their Absolute Configuration."

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] S. Sakai,: Springer-Verlag. The Alkaloids in"Natural Products of Woody Plants", 58 pages (1989)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] N. Aimi,: Academic Press. Alkaloids of Strychnos and Gardneria Species in "The Alkaloids", 68 pages (1989)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 1993-08-12  

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