| ID | 67611 |
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| Author |
Abe, Takumi
Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
ORCID
Kaken ID
researchmap
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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 | |
| Web of Science KeyUT | |
| 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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