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- W4200184902 endingPage "13889" @default.
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- W4200184902 abstract "Abstract The reaction between Oxone® and various di(hetero)aryl or alkyl diselenides enables the formation of an electrophilic selenium species in situ capable to induce the oxyselenocyclization of 2‐allylphenols. This versatile and safe protocol was explored to combine two privileged scaffolds into the structure of products: the 2,3‐dihydrobenzofuran core and an organoselenium moiety. Fifteen 2‐[(organoselanyl)methyl]‐2,3‐dihydrobenzofurans were produced, broadening considerably the number of known examples of this hybrid compound. Moreover, preparation of sulfur and tellurium 2,3‐dihydrobenzofurans derivatives was also successfully demonstrated." @default.
- W4200184902 created "2021-12-31" @default.
- W4200184902 creator A5025421462 @default.
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- W4200184902 creator A5056907094 @default.
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- W4200184902 creator A5086499358 @default.
- W4200184902 date "2021-12-22" @default.
- W4200184902 modified "2023-09-26" @default.
- W4200184902 title "Oxyselenocyclization of 2‐Allylphenols for the Synthesis of 2,3‐Dihydrobenzofuran Selenides" @default.
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