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  1. 原著論文

Synthesis of quaternary succinimides promoted by Ferric Nitrate

https://repo.qst.go.jp/records/73403
https://repo.qst.go.jp/records/73403
333236d4-3436-4eee-91cc-2bf1fb328fde
Item type 学術雑誌論文 / Journal Article(1)
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

WEKO 747353

Cai-Ling, Fan

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Kuan, Hu

× Kuan, Hu

WEKO 747354

Kuan, Hu

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Jing-Lin, Wang

× Jing-Lin, Wang

WEKO 747355

Jing-Lin, Wang

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Xin-Qi, Hao

× Xin-Qi, Hao

WEKO 747356

Xin-Qi, Hao

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Jun-Jie, Wei

× Jun-Jie, Wei

WEKO 747357

Jun-Jie, Wei

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Mao-Ping, Song

× Mao-Ping, Song

WEKO 747358

Mao-Ping, Song

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Zheng, Chao

× Zheng, Chao

WEKO 747359

Zheng, Chao

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Kuan, Hu

× Kuan, Hu

WEKO 747360

en 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
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
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