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Synthesis of quaternary succinimides promoted by Ferric Nitrate
https://repo.qst.go.jp/records/73403
https://repo.qst.go.jp/records/73403333236d4-3436-4eee-91cc-2bf1fb328fde
Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2019-02-06 | |||||
タイトル | ||||||
タイトル | Synthesis of quaternary succinimides promoted by Ferric Nitrate | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
アクセス権 | ||||||
アクセス権 | metadata only access | |||||
アクセス権URI | http://purl.org/coar/access_right/c_14cb | |||||
著者 |
Cai-Ling, Fan
× Cai-Ling, Fan× Kuan, Hu× Jing-Lin, Wang× Xin-Qi, Hao× Jun-Jie, Wei× Mao-Ping, Song× Zheng, Chao× Kuan, Hu |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | An efficient protocol has been accomplished for the synthesis of quaternary α-aminosuccinimides in toluene medium involving 2-phenylimidazo[1, 2-a]pyridine in a one-pot reaction promoted by Ferric Nitrate at 120 °C. The protocol presented herein, is for the first time, via a novel transformation where Ferric Nitrate promotes imidazo[1,2-a]pyridine structural metamorphosis to the title compound quaternary succinimides. High compatibility, easy work-up, and excellent yields are the advantages of this protocol. The quaternary α-aminosuccinimides are expected to have great potential in synthesizing quaternary α-amino acids and applications in medicinal chemistry. | |||||
書誌情報 |
Tetrahedron Letters 巻 59, 号 52, p. 4606-4610, 発行日 2018-11 |
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出版者 | ||||||
出版者 | Elsevier | |||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 0040-4039 | |||||
DOI | ||||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1016/j.tetlet.2018.11.043 |