Iodine-catalyzed thioallylation of indoles using Bunte salts prepared from Baylis-Hillman bromides

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Abstract

Metal-free iodine-catalyzed regioselective thioallylation of indoles has been accomplished at room temperature using Bunte salts prepared from Baylis-Hillman bromides. The resulting multi-functional C3 thioallylated indoles exhibit ample structural diversity and good functional group tolerance.

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Gupta, P. K., Yadav, A. K., Sharma, A. K., & Singh, K. N. (2021). Iodine-catalyzed thioallylation of indoles using Bunte salts prepared from Baylis-Hillman bromides. Organic and Biomolecular Chemistry, 19(15), 3484–3488. https://doi.org/10.1039/d1ob00377a

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