Research for Synthetic Utilization of Easily Available C_2-Symmetric Chiral Compounds
| Project/Area Number |
02670958
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
Chemical pharmacy
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| Research Institution | Gifu Pharmaceutical University |
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Principal Investigator |
MASAKI Yukio Gifu Pharm. Univ. Professor, 薬学部, 教授 (20082977)
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| Co-Investigator(Kenkyū-buntansha) |
ITOH Akichika Gifu Pharm. Univ. Instructur, 薬学部, 助手 (10203126)
ODA Hirohisa Gifu. Pharm. Univ. Instructor, 薬学部, 助手 (30106439)
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| Project Period (FY) |
1990 – 1991
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| Project Status |
Completed (Fiscal Year 1991)
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| Budget Amount *help |
¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 1991: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 1990: ¥1,500,000 (Direct Cost: ¥1,500,000)
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| Keywords | Tartaric Acid / D-Mannitol / (+)-Asperlin / Tartarimide / C_2-Symmetric Chiral Pyrrolidine / Total Synthesis / Chiral Ligand / C_2対称不斉素子 / 光学活性天然物の合成 / C_2対称不斉イミド |
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| Research Abstract |
In the research supported by this grant for two years term from April 1990 to March 1992, we have succeeded in the total synthesis of antibiotic(+)-asperlin(4)with antitumore activity staring with(-)-tartaric acid(1). The strategy included derivation to and effective utilization of 6, 8-dioxabicyclo[3.2. lloctane skeleton(3)as a key intermediate which is transformed highly site- and stereoselectively, and will serve as a general synthetic method for optically active 6-substituted 5-hydroxy-5, 6-dihydro-2-pyrones. In the project for development of chiral reagents from tartaric acid, 0, 0dibenzoyl-tartarimide(5)was syntesized in a 3-steps sequence and a high yield, and derived to the N-bromoimide(6). Bromoetherification of styrene by use of the N-bromoimide(6)was tried but unsuccessful in chiral induction. D-Mannitol(2)was transformed in a 2-steps sequence to chiral C_2-symmetric pyrrolidine(7), which was converted in short-steps sequences into several kinds of C_2-symmetric pyrrolidines(8)and D_2-symmetric ones(9). Examination of these pyrrolidines as chiral catalyst ligands was performed in the addition reaction of diethylzinc to benzaldehyde and a high chiral induction of 82% ee was attained with one of these pyrrolidines. In the research for exploitation of new reagent for natural product synthesis, we found a combination system of ethyl cyanoformate/30% hydrogen peroxide as a useful olefin-epoxidizing system which appears to be very mild and applicable to substrates bearing acid-labile functional groups.
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Report
(3 results)
Research Products
(11 results)
