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

Simple item page
dc.contributor.authorPrince Kumar Gupta
dc.contributor.authorArvind Kumar Yadav
dc.contributor.authorAnup Kumar Sharma
dc.contributor.authorKrishna Nand Singh
dc.date.accessioned2026-02-07T10:40:54Z
dc.date.issued2021
dc.description.abstractMetal-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. © The Royal Society of Chemistry 2021.
dc.identifier.doi10.1039/d1ob00377a
dc.identifier.issn14770520
dc.identifier.urihttps://doi.org/10.1039/d1ob00377a
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/37837
dc.publisherRoyal Society of Chemistry
dc.titleIodine-catalyzed thioallylation of indoles using Bunte salts prepared from Baylis-Hillman bromides
dc.typePublication
dspace.entity.typeArticle

Files

Collections

2021
An Initiative by BHU – Central Library
Powered by Dspace