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- W2097066562 endingPage "369" @default.
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- W2097066562 abstract "A novel approach to the synthesis of β-substituted dialkyl diselenides and selenides is described through reaction of bis(trimethylsilyl)selenide with epoxides, thiiranes, and aziridines catalyzed by tetrabutylammonium fluoride. Selective formation of a wide variety of β-hydroxy, β-mercapto, and β-amino diselenides and selenides is achieved by controlling the reaction conditions in the regioselective attack of the silyl selenide onto the ring-strained heterocycles. All reactions occur in a highly regioselective and enantioconservative manner, affording the title compounds with good to high yields. Selenium-77 NMR chemical shifts were measured to verify the selective formation of the β-substituted diselenides and selenides." @default.
- W2097066562 created "2016-06-24" @default.
- W2097066562 creator A5010751411 @default.
- W2097066562 creator A5016424809 @default.
- W2097066562 creator A5033687864 @default.
- W2097066562 date "2014-11-21" @default.
- W2097066562 modified "2023-10-03" @default.
- W2097066562 title "Bis(trimethylsilyl)selenide in the Selective Synthesis of β-Hydroxy, β-Mercapto, and β-Amino Diorganyl Diselenides and Selenides Through Ring Opening of Strained Heterocycles" @default.
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- W2097066562 doi "https://doi.org/10.1002/ejoc.201403015" @default.
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