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- W3196817557 endingPage "24291" @default.
- W3196817557 startingPage "24284" @default.
- W3196817557 abstract "Thiophene-based rings are one of the most widely used building blocks for the synthesis of sulfur-containing molecules. Inspired by the redox diversity of these features in nature, we demonstrate herein a redox-divergent construction of dihydrothiophenes, thiophenes, and bromothiophenes from the respective readily available allylic alcohols, dimethyl sulfoxide (DMSO), and HBr. The redox-divergent selectivity could be manipulated mainly by controlling the dosage of DMSO and HBr. Mechanistic studies suggest that DMSO simultaneously acts as an oxidant and a sulfur donor. The synthetic potentials of the products as platform molecules were also demonstrated by various derivatizations, including the preparation of bioactive and functional molecules." @default.
- W3196817557 created "2021-09-13" @default.
- W3196817557 creator A5005449100 @default.
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- W3196817557 creator A5072672952 @default.
- W3196817557 creator A5077230478 @default.
- W3196817557 creator A5080160303 @default.
- W3196817557 date "2021-10-04" @default.
- W3196817557 modified "2023-10-03" @default.
- W3196817557 title "Redox‐Divergent Construction of (Dihydro)thiophenes with DMSO" @default.
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