| Project/Area Number |
09672136
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Chemical pharmacy
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| Research Institution | Tohoku University |
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Principal Investigator |
IHARA Masataka Tohoku University, Faculty of Pharmaceutical Sciences, Professor, 薬学部, 教授 (00006339)
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| Project Period (FY) |
1997 – 1998
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| Project Status |
Completed (Fiscal Year 1998)
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| Budget Amount *help |
¥3,400,000 (Direct Cost: ¥3,400,000)
Fiscal Year 1998: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 1997: ¥1,900,000 (Direct Cost: ¥1,900,000)
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| Keywords | Intramolecular Cascade Reactio / Dimino Reaction / Stereoselective Synthesis / Polycyclic Compounds / Intramolecular Double Michael Reaction / Terpenes / Alkaoids / Cedranes / 分子内連続反応 / 多環状有機化合物 / セスキテルペン / アルカロイド / タカモニン / セドランジオール / クルモリン |
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| Research Abstract |
Cascade reactions forming multiple bonds in a stereo- and regio-selective manner by one procedure is one of the most ideal process in organic synthesis. The cascade reaction is also called as domino and tandem reaction. We have already developed two types of cascade reactions, which are useful for natural products synthesis. Thus, the intramolecular double Michael reaction of a compound having two types of unsaturated carbonyl groups provides a ploycyclic compound fused to six membered ring possessing five stereogenic centers. On the other hand, the intramolecular Michael-aldol reaction of the keto unsaturated ester constructs a polycyclic ring system fused to four membered ring having four stereogenic centers. These cascade reactions could be carried out under five different conditions using lithium hexamethyldisilazide or combinations of Lewis acids and Lewis amines. They have various advantages due to both merits of intramolecular reaction and cascade reaction. In this project, we achieved following total syntheses of natural products possessing important biological
(1) Synthesis of Indole Alkaloid, Tacamonine
Treatment of an indole derivative having an alpha, beta-unsaturated ester function at the C-2 position and an unsaturated amide group at the C-3 position with TBSOTf in the presence of triethylamine provided the indoloquinolizidine derivative. Synthesis of tacamonine was carried out in a facile manner from the product.
(2) Synthesis of Sesquiterpenoids, Cedranediol and Cedranoxide
Intramolecular double Michael reaction of 5-substituted cyclopentenone gave tricyclo[5.2.1 .0^<1.5>]decane, which was converted into cedranediol and cedranoxide.
(3) Synthesis of Sesquiterpenoid, Culmorine
An effective total synthesis of culmorine was accomplished via the intramolecular double Michael reaction of 4-substituted cyclopentenone as key step.
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