| Project/Area Number |
04640506
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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 |
有機化学一般
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| Research Institution | The University of Tokushima |
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Principal Investigator |
KAWAMURA Yasuhiko The University of Tokushima, Faculty of Engineering, Assistant Professor, 工学部, 講師 (30183289)
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| Project Period (FY) |
1992 – 1993
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| Project Status |
Completed (Fiscal Year 1993)
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| Budget Amount *help |
¥2,200,000 (Direct Cost: ¥2,200,000)
Fiscal Year 1993: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 1992: ¥1,100,000 (Direct Cost: ¥1,100,000)
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| Keywords | Nonvertical radical cation / Nitrone / Oxaziridine / Phosphorus ylide / Sulfur ylide / Hydroxyacetophenone / Photosensitized electron transfer / Single electron transfer / オキサジソジン / ホスホラン / ラジカルカチオン / 転位反応 |
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| Research Abstract |
In order to gain insight into the structure and reactivity of the above novel radical cations, nitrones (1)-oxaziridines (2), stable phosphorus (3) and sulfur ylides (4), and hydroxyacetophenones (5) were chosen as the substrates and photo and thermal single electron-transfer (SET) reactions were studied. The results are summarized as follows :
1. Compound 1 and 2 were interconvertable each other depending on the substituent on the aryl group under photosensitized electron-transfer (PET) conditions.
2. Ring-opening of 2 were proceeded in a stereoselective manner under PET conditions. It is also applicable to the convenient preparation of sterically hindered 1.
3. Although stable 3 are employed for the synthesis in a very limited scope, SET nature of such ylides are focused to enhance the reactivity. The reaction of fluorene substituted 3 with prenyloxybenzene diazonium salt gave dihydrobenzofuran derivative. The reaction proceeded via the SET-radical couplingionic termination sequence. Additionally, (cyclo)addition reactions of 3 with electron-deficient alkenes and alkynes were studied to aim at enhancing the reactivity by charge-transfer nature. Unusual temperature-dependence of NMR of fluorenylideneethylidene substituted 3 was also studied in comparison with the analogously substituted 4.
4. Photoreactivity of 5 which usually is unreactive upon photoirradiation were enhanced in the presence of aluminum halides. In one case, bromination of the neighboring alkyl group occurred in anti-Markownikoff manner. In another, remarkable structural conversion into oxabicycloheptenone occurred under PET conditions. The reaction seemed to be proceeded by the SET and the following addition of oxygen.
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