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2000 Fiscal Year Final Research Report Summary

A NEW DEVELOPMENT OF SYNTHETIC ORGANIC CHEMISTRY FOR BIOLOGICALLY ACTIVE NATURAL PRODUCTS OF MARINE ORIGINS

Research Project

Project/Area Number 10308027
Research Category

Grant-in-Aid for Scientific Research (A).

Allocation TypeSingle-year Grants
Section一般
Research Field Bioorganic chemistry
Research InstitutionHOKKAIDO UNIVERSITY

Principal Investigator

MURAI Akio  Hokkaido Univ., Grad.School of Sci., Prof., 大学院・理学研究科, 教授 (20000838)

Project Period (FY) 1998 – 2000
Keywords(+)-obtusenyne / condensed polycyclic ether / ciguatoxin / total synthesis / polycavernoside A / pinnatoxins / pectenotoxins / epoxy alcohol
Research Abstract

1) The first total synthesis of (+)-obtusenyne isolated from a red alga, Laurencia obtusa, has been achieved. Furthermore, two isomers of obtusenyne, which had been isolated by None and undetermined stereochemically, were totally synthesized. These results led to establishment of the absolute configuration of these compounds.
2) The synthetic route has been established toward realization of the proposed biosynthetic pathway for condensed cyclic polyether compounds of marine sources. Eventually, construction of the condensed bicyclic and tricyclic ether compounds were carried out firstly in endo-fashions starting from the corresponding polyepoxy alcohols as the models.
3) Two new efficient methods have been established in order to construct convergently two-condensed cyclic ethers.
4) The synthetic studies were developed toward the total synthesis of ciguatoxin which is the causative compound for ciguatera intoxication. The synthetic strategy was based on the convergent procedure to synthe … More size the four respective fragments and then to combine them constructing three residual 6-7-membered cyclic ether systems (CD,GH,JK). The synthesis of the CD and JK ring systems has been already achieved.
5) The first total synthesis of polycavernoside A isolated from a red alga, Polycavernosa tsudai, regarding as a causative compound for human intoxication, has been achieved. Furthermore, the structure-biological activity relationship has been clarified.
6) The study toward the total synthesis of pinnatoxins causing shell-fish poisoning originated from Pinna attenuata has been developed. Resultingly, the 1-step construction of the common BCDEF-ring system has been achieved. Furthermore, the strategy for construction of the AG-ring system has been established using an intermolecular Diels-Alder reaction by the model experiments.
7) The study toward the total synthesis of pectenotoxins causing shell-fish poisoning originated from Patinopecten yessoensis has been developed. Resultingly, all the fragments were able to be constructed except the C30 position. Less

  • Research Products

    (24 results)

All Other

All Publications (24 results)

  • [Publications] K.Fujiwara: "La(OTf)_3-Catalyzed 7-endo and 8-endo Selective Cyclizations of Hydroxy Epoxides"Tetrahedron Lett.. 39・5/6. 393-396 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] J.Ishihara: "Studies on the Stability of 1,7,9-Trioxadispiro [5.1.5.2] pentadecane System : The Common Tricyclic Acetal Moiety of Pinnatoxins"Synlett. No.6. 603-606 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] K.Fujiwara: "Total Synthesis and Absolute Configuration of Polycavernoside A"J.Am.Chem.Soc.. 120・41. 10770-10771 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] K.Fujiwara: "Chemical Realization of the Biogenetic Pathways Proposed for the Fused-Polycyclic Ethers of Marine Origins"Heterocycles. 50・1. 561-593 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] K.Fujiwara: "Total Synthesis of (+)-Obtusenyne"J.Org.Chem.. 64・8. 2616-2617 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] T.Sugimoto: "Synthesis of the B,C,D,E,F-Ring Fragment of Pinnatoxins"Synlett. No.5. 541-544 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] D.Awakura: "Determination of the Absolute Configurations of Norte's Obtusenynes by Total Syntheses of (12R,13R)-(-)- and (12S,13R)-(+)-Obtusenynes"Chemistry Lett.. No.6. 461-462 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] K.Fujiwara: "A Simple Convergent Method for the Construction of Fused Tri-and Tetracyclic Ethers"Synlett. No.7. 1037-1040 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] L.Barriault: "Synthesis and Biological Evaluation of Analogues of the Marine Toxin Polycavernoside A"Bioorg.Med.Chem.Lett.. No.9. 2069-2072 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] K.Fujiwara: "Four-Step Convergent Synthesis of trans-Fused Tetracyclic Oxane"Tetrahedron Lett.. 41・4. 507-508 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] T.Tokiwano: "Biomimetic Construction of Fused Tricyclic Ether by Cascaded endo-Cyclization of the Hydroxy Triepoxide"Synlett. No.3. 329-332 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] D.Awakura: "Synthetic Studies on Pectenotoxins : Synthesis of the Common C8-C18 THF Fragment"Synlett. No.12. 1733-1736 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] K.Fujiwara: "La(OTf)_3-Catalyzed 7-endo and 8-endo Selective Cyclizations of Hydroxy Epoxides"Tetrahedron Lett.. 39 5/6. 393-396 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] J.Ishihara: "Studies on the Stability of 1,7,9-Trioxadispiro[5.1.5.2]pentadecane System : The Common Tricyclic Acetal Moiety of Pinnatoxins"Synlett. No.6. 603-606 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] K.Fujiwara: "Total Synthesis and Absolute Configuration of Polycavernoside A"J.Am.Chem.Soc.. 120 41. 10770-10771 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] K.Fujiwara: "Chemical Realization of the Biogenetic Pathways Proposed for the Fused-Polycyclic Ethers of Marine Origins"Heterocycles. 50 1. 561-593 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] K.Fujiwara: "Total Synthesis of (+)-Obtusenyne"J.Org.Chem.. 64 8. 2616-2617 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] T.Sugimoto: "Synthesis of the B,C,D,E,F-Ring Fragment of Pinnatoxins"Synlett. No.5. 541-544 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] D.Awakura: "Determination of the Absolute Configurations of Norte's Obtusenynes by Total Syntheses of (12R, 13R)-(-)- and (12S, 13R)-(+)-Obtusenynes"Chemistry Lett.. No.6. 461-462 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] K.Fujiwara: "A Simple Convergent Method for the Construction of Fused Tri- and Tetracyclic Ethers"Synlett. No.7. 1037-1040 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] L.Barriault: "Synthesis and Biological Evaluation of Analogues of the Marine Toxin Polycavernoside A"Bioorg.Med.Chem.Lett.. No.9. 2069-2072 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] K.Fujiwara: "Four-Step Convergent Synthesis of trans-Fused Tetracyclic Oxane"Tetrahedron Lett.. 41 4. 507-508 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] T.Tokiwano: "Biomimetic Construction of Fused Tricyclic Ether by Cascaded endo-Cyclization of the Hydroxy Triepoxide"Synlett. No.3. 329-332 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] D.Awakura: "Synthetic Studies on Pectenotoxins : Synthesis of the Common C8-C18 THF Fragment"Synlett. No.12. 1733-1736 (2000)

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

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Published: 2002-03-26  

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