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- W2971425192 endingPage "15679" @default.
- W2971425192 startingPage "15675" @default.
- W2971425192 abstract "Abstract Due to their ubiquity in nature and frequent use in organic electronic materials, benzothiophenes are highly sought after. Here we set out an unprecedented procedure for the formation of benzothiophenes by the twofold vicinal C−H functionalization of arenes that does not require metal catalysis. This one‐pot annulation proceeds through an interrupted Pummerer reaction/[3,3]‐sigmatropic rearrangement/cyclization sequence to deliver various benzothiophene products. The procedure is particularly effective for the rapid synthesis of benzothiophenes from non‐prefunctionalized polyaromatic hydrocarbons (PAHs)." @default.
- W2971425192 created "2019-09-12" @default.
- W2971425192 creator A5020445688 @default.
- W2971425192 creator A5032096939 @default.
- W2971425192 creator A5039602253 @default.
- W2971425192 creator A5040225377 @default.
- W2971425192 date "2019-09-24" @default.
- W2971425192 modified "2023-10-05" @default.
- W2971425192 title "Metal‐Free Synthesis of Benzothiophenes by Twofold C−H Functionalization: Direct Access to Materials‐Oriented Heteroaromatics" @default.
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