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. Author manuscript; available in PMC: 2022 Nov 20.
Published in final edited form as: J Am Chem Soc. 2022 Apr 29;144(18):8296–8305. doi: 10.1021/jacs.2c02392

Figure 3.

Figure 3.

Decarboxylative bromination and iodination of (hetero)aryl carboxylic acids. Bromination conducted with 1,3-dibromo-5,5-dimethylhydantoin (0.75 equiv) unless otherwise specified. Iodination conducted with N-iodosuccinimide (1 equiv). aWith BrCCl3 (3 equiv) as bromination reagent. See Supporting Information for additional examples and experimental details.