| Project/Area Number |
07458141
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Bioorganic chemistry
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| Research Institution | Tokyo Institute of Technology |
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Principal Investigator |
TAKAHASHI Takashi Tokyo Institute of Technology, Department of Chemical Engineering, Professor, 工学部, 教授 (80110724)
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| Co-Investigator(Kenkyū-buntansha) |
DOI Takayuki Tokyo Institute of Technology, Department of Chemical Engineering, Assistant Pro, 工学部, 助手 (90212076)
YAMADA Haruo Tokyo Institute of Technology, Department of Chemical Engineering, Associate Pro, 工学部, 助教授 (10175664)
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| Project Period (FY) |
1995 – 1997
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| Project Status |
Completed (Fiscal Year 1997)
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| Budget Amount *help |
¥7,700,000 (Direct Cost: ¥7,700,000)
Fiscal Year 1997: ¥400,000 (Direct Cost: ¥400,000)
Fiscal Year 1996: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 1995: ¥6,100,000 (Direct Cost: ¥6,100,000)
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| Keywords | taxol / antitumor / transannular reaction / biosynthesis / molecular design / moleculer mechanics / intramolecular alkylation / 12-membered ring |
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| Research Abstract |
Taxol, originally isolated from the Pacific yew (Taxus brevifolia), has shown remarkable potential in recent clinical trials for the treatment of breast and ovarian cancer. Its structural complexity and the limited availability have engendered world-wide intensive studies toward its total synthesis. We accomplished the three efficient approaches toward the synthesis of taxol on the basis of molecular design using molecular mechanics calculations : 1. Stereoselective synthesis of 12-membered ring enepoxide that is a biomimetic taxol intermediate was achieved. Lewis acidcatalyzed transannular cyclization gave cyclized adduct which, however, underwent over reaction leading to a rearrangement product. 2. intramolecular alkylation of the cyanohydrin ether was found to be an efficient method preparing an 8-membered ring corresponding to the B-ring of taxoid system. This method was efficiently applied to the synthesis of A-B-C rings of taxane skeleton ; 3. (3+2) -cycloaddition of nitrile oxide that is a key reaction preparing the C-ring of taxol system was successfully carried out forming an 8beta-methyl group on the C-ring with complete stereoselection. This method was utilized in the synthesis of fully functionalized CD-rings of the taxane system leading to a very important synthetic intermediate toward the total synthesis of taxol.
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