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ID 67611
フルテキストURL
fulltext.pdf 9.04 MB
著者
Abe, Takumi Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University ORCID Kaken ID researchmap
抄録
Azide-containing compounds, organic azides, showcases a variety of reactivities, making them highly convenient and chameleonic intermediates. An indoline derivative has been proven to be of great significance in drug discovery due to its sp3-rich property. In this context, it is interesting to perform such vigorous azidation on medicinal-relevant indoles/indolines, resulting in the production of sp3-rich azidoindolines. The potential biological activity, in combination with the sp3-rich indoline bearing the azido moiety, makes azidoindolines an attractive synthetic target for medicinal and synthetic chemists. This review describes recent advances in the synthesis and application of azidoindolines: (1) iodine-mediated azidations, (2) metal-catalyzed azidations, (3) electrochemical azidations, (4) photochemical azidations, (5) azidation using a combination of an oxidant and an azide source, and (6) nucleophilic azidation.
キーワード
azidoindolines
indole
azido
synthesis
application
発行日
2024-07-18
出版物タイトル
Chemistry
6巻
4号
出版者
MDPI
開始ページ
556
終了ページ
580
ISSN
2624-8549
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© 2024 by the author.
論文のバージョン
publisher
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.3390/chemistry6040034
ライセンス
https://creativecommons.org/licenses/by/4.0/
Citation
Abe, T. Azidoindolines—From Synthesis to Application: A Review. Chemistry 2024, 6, 556-580. https://doi.org/10.3390/chemistry6040034
助成機関名
Japan Society for the Promotion of Science
助成番号
22K06503