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• W3033596352 endingPage "131311" @default.
• W3033596352 startingPage "131311" @default.
• W3033596352 abstract "A study by our laboratory shows that air, light and moisture stable O-(tert-butyl) Se-phenyl selenocarbonate could be employed as a safer, practical and efficient alternative to generate “in situ” benzeneselenol or benzeneselenolate anion under different and transition metal-free conditions. This procedure seems to be of general application since the nucleophilic selenium species obtained can be trapped by electrophiles such as alkyl halides, epoxides and electron-deficient alkenes and alkynes under different reaction conditions." @default.
• W3033596352 created "2020-06-12" @default.
• W3033596352 creator A5006784510 @default.
• W3033596352 creator A5082015832 @default.
• W3033596352 date "2020-07-01" @default.
• W3033596352 modified "2023-10-12" @default.
• W3033596352 title "O-(tert-butyl) Se-phenyl selenocarbonate: A convenient, bench-stable and metal-free precursor of benzeneselenol" @default.
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• W3033596352 doi "https://doi.org/10.1016/j.tet.2020.131311" @default.
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