| Project/Area Number |
01850193
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| Research Category |
Grant-in-Aid for Developmental Scientific Research (B).
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| Allocation Type | Single-year Grants |
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| Research Field |
Synthetic chemistry
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| Research Institution | Kyoto University |
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Principal Investigator |
MATSUMUR Yoshihiro Kyoto University, Faculty of Engineering, Associate Professor, 工学部, 助教授 (60026309)
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| Co-Investigator(Kenkyū-buntansha) |
KISE Naoki Kyoto University, Faculty of Engineering, Assistant Professor, 工学部, 助手 (90177824)
KASHIMURA Shigenori Kyoto University, Faculty of Engineering, Assistant Professor, 工学部, 助手 (50152632)
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| Project Period (FY) |
1989 – 1990
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| Project Status |
Completed (Fiscal Year 1990)
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| Budget Amount *help |
¥7,100,000 (Direct Cost: ¥7,100,000)
Fiscal Year 1990: ¥2,300,000 (Direct Cost: ¥2,300,000)
Fiscal Year 1989: ¥4,800,000 (Direct Cost: ¥4,800,000)
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| Keywords | Anodic Oxidation / Cathodic Reduction / Pyrrolidine / Piperidine / Alkaloid / Decyanation / アルカロイド / 脱シアノ化 |
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| Research Abstract |
The main results obtained in the research were as follow ; i) Lewis acid treatment of anodically prepared dimethyl N-methoxycarbonyl-N-methoxymethylaminomalonate with aryl olefins afforded beta -aryl- pyrrolidine derivatives, and one of the products was successfully converted to mesembrine. ii) An alkyl group was introduced to the alpha' position of alpha-substituted pyrrolidines with high diastereoselectivities by modifying the alpha'-substituents or the functional groups located at the nitrogen atom of pyrrolidine ring. iii) Optically active N-methylpsuedconhidrine was synthesized by anodic beta -acetoxylation of piperidine derivatives. iv) Regioselective alkylation on a piperidine ring was achieved by using beta, gamma-unsatureated N-alkoxycarbonylpiperidines which were prepared from N-alkoxycarbonylpiperidinesby utilizing anodic oxidation in a key step, and this reaction was applied to the synthesis of meroquinene, etc. v) Nitrogen-containing bicyclic compounds were synthesized by the reaction of alpha, alpha' -di- cation or alpha, gamma- dication equivalents with dianion equivalents. vi) Conditions for the efficient electroreductive decyanation were found and they were applied to the synthesis of alpha-substituted pyrrolidine and piperidine derivatives. vii) A new route for the generation of alpha -amino carbanions was exploited.
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