2002 Fiscal Year Final Research Report Summary
Development of Catalytic Asymmetric Careade Reaction and Its Application to Total Syntheses of Bioactive Compounds
| Project/Area Number |
13470466
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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 |
Chemical pharmacy
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| Research Institution | Tohoku University |
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Principal Investigator |
IHARA Masataka Tohoku University, Graduate School of Pharmaceutical Sciences, Professor, 大学院・薬学研究科, 教授 (00006339)
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| Co-Investigator(Kenkyū-buntansha) |
TAKASU Kiyosei Tohoku University, Graduate School of Pharmaceutical Sciences, Assistant, 大学院・薬学研究科, 助手 (10302168)
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| Project Period (FY) |
2001 – 2002
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| Keywords | Cascade Reaction / Asymmetric Synthesis / Stereo Chemistry / Transition Metal Catalysed Reaction / Bioactive Compounds / Intramolecular Double Michael Reaction / Intramolecular Michael-Aedol Reaction / Fixation of Carbon Dioxide |
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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. We have been studying constructions of polycyclic ring systems by using cascade reaction under four different conditions, ionic reaction, radical reaction, transition metal catalyzed reaction and furthermore pericyclic reaction. we have already developed two types of cascade reactions, which are useful for natural products synthesis. Thus, intramolecular double Michael reaction provides a ploycyclic compound fused to six membered ring possessing five stereogenic centers. On the other hand, the intramolecular Michael-aldol reaction constructs polycyclic ring systems fused to four membered ring having multiple stereogenic centers. Catalytic asymmetric reactions of these cascade reactions were extensively studied.
Recently, we have developed a new type of palladium-catalyzed cascade reaction ; treatment of propalgyl carbonate with phenol in the presence of catalytic amount of zero valence palladium producing a cyclic carbonate. The reaction has been easily extended to asymmetric synthesis using (S)-BINAP with high enantio selectivity.
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