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- W2937888901 endingPage "8783" @default.
- W2937888901 startingPage "8779" @default.
- W2937888901 abstract "Abstract A transition metal‐free one‐pot stereoselective approach to substituted ( E , Z )‐1,3‐dienes was developed by using an interrupted Pummerer reaction/ligand‐coupling strategy. Readily available benzothiophene S‐oxides, which can be conveniently prepared by oxidation of the parent benzothiophenes, undergo Pummerer coupling with styrenes. Reaction of the resultant sulfonium salts with alkyllithium/magnesium reagents generates underexploited hypervalent sulfurane intermediates that undergo selective ligand coupling, resulting in dismantling of the benzothiophene motif and the formation of decorated ( E , Z )‐1,3‐dienes." @default.
- W2937888901 created "2019-04-25" @default.
- W2937888901 creator A5003772806 @default.
- W2937888901 creator A5032096939 @default.
- W2937888901 creator A5040225377 @default.
- W2937888901 creator A5048370251 @default.
- W2937888901 date "2019-06-07" @default.
- W2937888901 modified "2023-10-03" @default.
- W2937888901 title "Transition‐Metal‐Free Cross‐Coupling of Benzothiophenes and Styrenes in a Stereoselective Synthesis of Substituted (<i>E,Z</i>)‐1,3‐Dienes" @default.
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