B2Pin2-Enabled Reductive Thioesterification of Aryl Triflates with Thiocarbonates

Abstract

In this work, we demonstrate a B₂Pin₂-mediated reductive coupling of aryl triflates with thiocarbonates for aryl thioester synthesis. This method surpasses previous Zn-based protocols, especially for pyridyl and sterically hindered 2,6-disubstituted arenes, likely due to distinct reduction pathways. Its utility is demonstrated in the thioesterification of pharmaceuticals (Apixaban, Ezetimibe, Ethinyl estradiol derivatives) under mild conditions. Furthermore, this work lays the foundation for B₂Pin₂-driven reductive C(sp²)-C(sp²) couplings using earth-abundant metals, offering a scalable alternative to traditional Zn/Mn reductants in industrial settings.

Supplementary files

Article information

Article type
Communication
Submitted
17 Jul 2025
Accepted
18 Sep 2025
First published
18 Sep 2025

Chem. Commun., 2025, Accepted Manuscript

B2Pin2-Enabled Reductive Thioesterification of Aryl Triflates with Thiocarbonates

H. Shi, F. Wu, W. Zhu, H. C. Shen, S. Xu, X. Wang and H. Gong, Chem. Commun., 2025, Accepted Manuscript , DOI: 10.1039/D5CC04038H

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