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DOI: 10.1055/a-1966-4974
Azidation with Hypervalent Iodine Reagents
We thank the Swiss National Science Foundation (sinergia CRSII5_171026) for financial support.
Dedicated to Prof. Cristina Nevado at the occasion of the awarding of the Dr. Margaret Faul Women in Chemistry Award 2021
Abstract
In this short review, we describe applications of hypervalent iodine reagents for the azidation of organic compounds from seminal publications to the most recent reports. After reviewing selected examples of azidations based on the use of in situ formed unstable non-cyclic reagents, we focus in more detail on stable cyclic hypervalent iodine reagents. Important advances in the azidation of C–H bonds, alkenes, as well as other transformations are described. Rather than being comprehensive, we highlight selected key reports that, in our opinion, especially contributed to the advancement of research in the field.
1 Introduction
2 Non-Cyclic λ3-Iodanes
3 Heterocyclic λ3-Iodanes
3.1 Azidation of Aliphatic C–H Bonds
3.2 Azidation of Alkenes
3.3 Other Azidations
4 Conclusion and Outlook
Key words
azidation - hypervalent iodine reagents - metal catalysis - photocatalysis - nucleoazidation - cyclizationPublikationsverlauf
Eingereicht: 21. September 2022
Angenommen nach Revision: 24. Oktober 2022
Accepted Manuscript online:
24. Oktober 2022
Artikel online veröffentlicht:
23. November 2022
© 2022. Thieme. All rights reserved
Georg Thieme Verlag KG
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This review also covers I(V) reagents, whereas we focus on I(III). For seminal examples of azidation using I(V) reagents, see: