缩醛
化学
季戊四醇
点击化学
催化作用
有机化学
高分子化学
阻燃剂
作者
Shuai Du,Shuaiqi Yang,Li Wang,Pengyun Li,Jin Zhu,Songqi Ma
标识
DOI:10.1002/anie.202405653
摘要
Dithioacetals are heavily used in organic, material and medical chemistries, and exhibit huge potential to synthesize degradable or recyclable polymers. However, the current synthetic approaches of dithioacetals and polydithioacetals are overwhelmingly dependent on external catalysts and organic solvents. Herein, we disclose a catalyst- and solvent-free acetal-thiol click-like reaction for synthesizing dithioacetals and polydithioacetals. High conversion, higher than acid catalytic acetal-thiol reaction, can be achieved. High universality was confirmed by monitoring the reactions of linear and cyclic acetals (including renewable bio-sourced furan-acetal) with aliphatic and aromatic thiols, and the reaction mechanism of monomolecular nucleophilic substitution (S
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