ID | 67611 |
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Author |
Abe, Takumi
Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
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Abstract | 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.
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Keywords | azidoindolines
indole
azido
synthesis
application
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Published Date | 2024-07-18
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Publication Title |
Chemistry
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Volume | volume6
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Issue | issue4
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Publisher | MDPI
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Start Page | 556
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End Page | 580
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ISSN | 2624-8549
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Content Type |
Journal Article
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language |
English
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OAI-PMH Set |
岡山大学
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Copyright Holders | © 2024 by the author.
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File Version | publisher
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DOI | |
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Related Url | isVersionOf https://doi.org/10.3390/chemistry6040034
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License | https://creativecommons.org/licenses/by/4.0/
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Citation | Abe, T. Azidoindolines—From Synthesis to Application: A Review. Chemistry 2024, 6, 556-580. https://doi.org/10.3390/chemistry6040034
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Funder Name |
Japan Society for the Promotion of Science
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助成番号 | 22K06503
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