Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 20, Issue 25, Pages 5009-5034Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ob00741j
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Funding
- CONACyT [FORDECYT-PRONACES/610286/2020]
- JSPS KAKENHI [19K05466]
- Ritsumeikan Global Innovation Research Organization (R-GIRO) project
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Iodine (III) reagents, with their characteristics of safety, environmental friendliness, and ease of use, have become important alternatives in organic synthesis. They have been widely used in the functionalization of various aromatic cores, introducing multiple functional groups. Furthermore, iodine (III) reagents have significant applications in metal-free arylation reactions.
Iodine(iii) reagents have attracted chemical relvance in organic synthesis by their use as safe, non-toxic, green and easy to handle reagents in different transformations. These characteristics make them important alternatives to procedures involving hazardous and harsh reaction conditions. Their versatility as oxidants has been exploited in the functionalization of different aromatic cores, which allow the introduction of several groups. Metal-free arylation using iodine(iii) reagents is by far one of the most described topics in the literature; however, other highly relevant non-aromatic groups have been also introduced. Herein, we summarize the most representative developed procedures for the functionalization of aryls and heteroaryls by introducing halogens, using different iodine(iii) reagents.
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