| Project/Area Number |
08455431
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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 |
Synthetic chemistry
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| Research Institution | Faculty of Engineering, Nagasaki University |
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Principal Investigator |
TAMURA Yoshinao Nagasaki University, Faculty of Engineering, Professor of Chem., 工学部, 教授 (80026319)
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| Co-Investigator(Kenkyū-buntansha) |
KIMURA Masanari Nagasaki University, Faculty of Engineering, Assistant Professor, 工学部, 助手 (10274622)
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| Project Period (FY) |
1996 – 1998
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| Project Status |
Completed (Fiscal Year 1998)
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| Budget Amount *help |
¥6,800,000 (Direct Cost: ¥6,800,000)
Fiscal Year 1998: ¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 1997: ¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 1996: ¥2,700,000 (Direct Cost: ¥2,700,000)
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| Keywords | p-Allylpalladium / Umpolung / Diethylzine / Allylation / beta-Decarbopalladation / omega-Dienyl Aldehydes / ジエン / 開環反応 / 安息香酸アリル / 安息香酸プロパルギル / アルデヒド |
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| Research Abstract |
pi-Allylpalladium is usually recognized to serve as synthetically important electrophilic allylating agent toward many nucleophiles (organometals). This research mechanistically clarified that pi-allylpalladium complexes, catalytically generated in situ by the reaction of allylic esters and Pd(O), undergo the alkyl ligand exchange with diethylzinc and provide a mixture of allylzinc and diethylpalladium species. The thus formed allylzinc demonstrated unique regio-and stereoselectivity for the reaction with carbonyl compounds. For example, 1,3-disubstituted allylzinc reacted with aldehyde to provide (Z)-anti-homoallyl alcohols with high stereoselectivity. Furthermore, the present methodology turned out to be very useful and powerful to generate stereochemically defined allylzinc species, the species being very difficult to generate by other methods. The similar umpolung reaction proceeds between pi-allylpalladium and triethylborane (unpublished results).
In the related research, it was demonstrated that pi-allylpalladium serves as an active species to promote beta-decarbopalladation reaction. This reaction also proceeds catalytically with respect to palladium and furnishes omega-dienyl aldehydes and ketones in good yields. Chemical & Engineering News picked up this report from the following points of view ; the uniqueness of the reaction type and the synthetic importance of the products as synthetic intermediates.
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