Demonstrates a metal-free method to synthesize β-arylthio-γ-butyrolactones, highlighting its advantages for synthetic chemistry.
γ-Butyrolactone (GBL) is an important structural motif commonly found in a wide range of natural products, bioactive molecules, agrochemicals, and fragrance compounds. In this study, a Lewis acid-assisted approach was developed to prepare β-arylthio-γ-butyrolactone skeletons using benzenesulfonyl chloride as a sulfur source. This approach requires no transition metal catalysts and provides several advantages, including mild reaction conditions, broad substrate scope, and good functional group compatibility.
No takes yet. Share an insight, caveat, or question.
Wang et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: