化学
芳构化
异构化
硫黄
催化作用
产量(工程)
亲核细胞
二苯并噻吩
有机化学
芳基
基质(水族馆)
亲核加成
组合化学
冶金
材料科学
地质学
海洋学
烷基
作者
Wenjing Yu,Chen‐Ho Tung,Zhenghu Xu
标识
DOI:10.1002/adsc.202200677
摘要
Abstract The synthesis of benzofurans from readily accessible sulfur ylides and ortho ‐hydroxy aryl alkynes is reported. The transformation proceeds through an isomerization/nucleophilic addition/cyclization/aromatization cascade. The substrate scope is very general with respect to both reactants and the products are afforded in 43–94% yield under conditions which are catalyst‐free and additive‐free. magnified image
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