Development of novel reactivitity of methylene acetals and its application to synthesis of heterocycles
| Project/Area Number |
26460023
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Chemical pharmacy
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| Research Institution | Kindai University |
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Principal Investigator |
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| Project Period (FY) |
2014-04-01 – 2017-03-31
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| Project Status |
Completed (Fiscal Year 2016)
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| Budget Amount *help |
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2016: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2015: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2014: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
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| Keywords | メチレンアセタール / エポキシド / N,O-アセタール / 脱保護反応 |
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| Outline of Final Research Achievements |
We developed a novel transformation reaction of methylene acetal using Phenylthiotrimethylsilane and N-bromosuccinimide. The reaction proceeded under mild conditions to afford the corresponding bromoformates, which could be converted to the corresponding epoxides by the treatment of NaOMe. This reaction was applicable to one-pot transformation from methylene acetal to eppoxide. The methylene acetal derived from aminoalcohol was also transformed under the same conditions giving the corresponding product.
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Report
(4 results)
Research Products
(3 results)
