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• W2801688714 endingPage "e4706" @default.
• W2801688714 startingPage "e4706" @default.
• W2801688714 abstract "A green methodology to synthesize 2-organoselanyl-naphthalenes based on the reaction of alkynols with diaryl diselenides is described. The electrophilic species of selenium were generated in situ, by the oxidative cleavage of the Se–Se bond of diaryl diselenides by Oxone ® using water as the solvent. The reactions proceeded efficiently under ultrasonic irradiation as an alternative energy source, using a range of alkynols and diorganyl diselenides as starting materials. Through this methodology, the corresponding 2-organoselanyl-naphthalenes were obtained in moderate to good yields (56–94%) and in short reaction times (0.25–2.3 h)." @default.
• W2801688714 created "2018-05-17" @default.
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• W2801688714 date "2018-05-07" @default.
• W2801688714 modified "2023-09-25" @default.
• W2801688714 title "Ultrasound-promoted synthesis of 2-organoselanyl-naphthalenes using Oxone^® in aqueous medium as an oxidizing agent" @default.
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• W2801688714 doi "https://doi.org/10.7717/peerj.4706" @default.
• W2801688714 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5944430" @default.
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