Issue 15, 2021

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

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.

Graphical abstract: Iodine-catalyzed thioallylation of indoles using Bunte salts prepared from Baylis–Hillman bromides

Supplementary files

Article information

Article type
Paper
Submitted
26 Feb 2021
Accepted
19 Mar 2021
First published
20 Mar 2021

Org. Biomol. Chem., 2021,19, 3484-3488

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

P. K. Gupta, A. K. Yadav, A. K. Sharma and K. N. Singh, Org. Biomol. Chem., 2021, 19, 3484 DOI: 10.1039/D1OB00377A

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