Inverse-Electron-Demand oxa-Diels–Alder Reactions of α-Keto-β,γ-unsaturated Esters and α,β-Unsaturated Hydrazones
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- Yoshimitsu Hashimoto
- Showa Pharmaceutical University, Machida, Tokyo 194-8543, Japan
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- Takanori Ikeda
- Showa Pharmaceutical University, Machida, Tokyo 194-8543, Japan
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- Ayako Ida
- Showa Pharmaceutical University, Machida, Tokyo 194-8543, Japan
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- Nobuyoshi Morita
- Showa Pharmaceutical University, Machida, Tokyo 194-8543, Japan
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- Osamu Tamura
- Showa Pharmaceutical University, Machida, Tokyo 194-8543, Japan
書誌事項
- 公開日
- 2019-05-29
- 資源種別
- journal article
- 権利情報
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- https://doi.org/10.15223/policy-029
- https://doi.org/10.15223/policy-037
- https://doi.org/10.15223/policy-045
- DOI
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- 10.1021/acs.orglett.9b01422
- 公開者
- American Chemical Society (ACS)
この論文をさがす
説明
A concise synthetic method for dihydropyrans has been developed by inverse-electron-demand oxa-Diels-Alder reaction of α-keto-β,γ-unsaturated esters with α,β-unsaturated hydrazones as electron-rich olefins. This reaction is catalyzed by Eu(hfc)
収録刊行物
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- Organic Letters
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Organic Letters 21 (11), 4245-4249, 2019-05-29
American Chemical Society (ACS)
