Unlocking the Potential of Tris(Pentafluorophenyl)Borane in Reductive Desulfurization of Thioamides With Silane
Year: 2025
Type: article
Abstract: Selective conversion of a functional group to a high‐value product, namely defunctionalization, is an important procedure in synthetic chemistry. Herein, we report the first transition metal‐free desulfurization of thioamides under relatively mild reaction conditions. The catalytic reaction proceeds with the selective cleavage of the C═S bonds of thioamides to furnish the corresponding amines in good to excellent yields with B(C 6 F 5 ) 3 and PhSiH 3 . The protocol is simple, does not require any additives, and encompasses a broad substrate scope with chemoselective reduction of vulnerable functional groups. To understand the mechanism, several control studies and detailed computational calculations were performed.
Source: Chemistry - A European Journal
Institution: Indian Institute of Technology Bhilai
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: bronze
Award: G4806791415
OpenAlex ID: W4409363117
