Catalyst Free Annulative Thioboration of Unfunctionalized Olefins
Overview
Affiliations
A direct and catalyst-free annulative thioboration of unfunctionalized olefins has been developed. In the presence of BCl as the sole boron source, the boryl group and thiol group are added to the C-C double bonds simultaneously. The boronic acids obtained can be protected to form synthetically ubiquitous pinacol boronate esters.
Computational study on catalyst-free BCl-promoted chloroboration of carbonyl compounds.
Derese A, Menkir M, Wolie M, Yemam D RSC Adv. 2025; 15(4):2862-2873.
PMID: 39877698 PMC: 11774190. DOI: 10.1039/d4ra06893a.
Transition-Metal-Free Thioboration of Terminal Alkynes.
Matsuyama T, Ishida H, Wang C, Miyamoto K, Nakajima M, Toriumi N JACS Au. 2024; 4(12):4927-4933.
PMID: 39735905 PMC: 11672135. DOI: 10.1021/jacsau.4c00907.