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Reactivity of Hypervalent Iodine(III) Reagents Bearing Transferable N‐Based Groups.

Authors :
Macara, João
Caldeira, Catarina
Poeira, Diogo L.
Marques, M. Manuel B.
Source :
European Journal of Organic Chemistry. 7/3/2023, Vol. 26 Issue 25, p1-24. 24p.
Publication Year :
2023

Abstract

Hypervalent iodine reagents have the ability of inverting the polarity of functional groups bound to iodine, a reactivity known as umpolung. This reactivity makes hypervalent iodine compounds highly attractive for the creation of electrophilic synthons of known nucleophiles, resulting in novel synthetic disconnections and the formation of new Nu(nucleophile)−N bond. Electrophilic sources of nitrogen‐based groups have been known for many decades and are of great synthetic importance. Traditionally, these reagents are limited to few examples. With the use of hypervalent iodine, the transfer of a wide diversity of nitrogen sources became a possibility. This review compiles the latest reported examples of hypervalent iodine reagents capable of electrophilic transfer of nitrogen‐based groups. It showcases the preparation of such reagents, their synthetic utility, and reaction mechanisms involving these group transfer reagents. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1434193X
Volume :
26
Issue :
25
Database :
Academic Search Index
Journal :
European Journal of Organic Chemistry
Publication Type :
Academic Journal
Accession number :
164682023
Full Text :
https://doi.org/10.1002/ejoc.202300109