| Project/Area Number |
06672090
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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 | Toyama University |
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Principal Investigator |
HIRAI Yoshiro Toyama University Faculty of Science, Professor, 理学部, 教授 (70111747)
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| Project Period (FY) |
1994 – 1995
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| Project Status |
Completed (Fiscal Year 1995)
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| Budget Amount *help |
¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 1995: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1994: ¥1,200,000 (Direct Cost: ¥1,200,000)
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| Keywords | stereoselective cyclization / trans (2,6) piperidine / cis (2,6) piperidine / palladium (II) catalyst / silver trifluoroacetate / (+) -prosopinine / (+) -pseudoconhydrine / (+) -palustrine / 2,6-cis-ピペリジン / (+)-palustrine / 分子内付加環化 / 有機銀塩 / 香月-Sharpless不斉酸化 / 2,6位トランスピペジリン / 2,6位シスピペリジン / (+)-pseudoconhydrine |
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| Research Abstract |
The intramolecular cyclization of the optically active urethanes containing allylic alkohol was effected by treatment with bis (acetonitrile) palladium (II) chloride to give the trans (2,6) piperidine system as a single diastereoisomer. During these transformations, the Pd (II) species are not reduced and thus the catalyst can recycle without its reoxidation. On the other hand, cyclization of the simillar substrate containing allylic chloride using silver trifluoroacetate in the presence of sodium hydride afforded the cis (2,6) piperidine system. Cyclization of other substrates using these transition metal complexes was aoso examined and simillar results were obtained.
The cyclo-adducts obtained were proved to be useful chiral building blocks by their conversion into (+) -prosopinine, (+) -pseudoconhydrine, and the important synthetic intermediate of (+) -palustrine, respectively
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