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- W2063374352 abstract "Various commercially available thiols react photochemically with tetravinylsilane to give the corresponding tetrasubstituted thioether compounds. The reactions are conducted in air using typical borosilicate glassware. Yields range from 64 to 100%, and purification steps, if necessary, involve simple precipitation or extraction steps. Thiol addition occurs predominantly to give the anti-Markovnikov product; amounts of Markovnikov addition range from 1 to 5%." @default.
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- W2063374352 date "2008-09-11" @default.
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- W2063374352 title "Thiol−Ene Reaction for the Synthesis of Multifunctional Branched Organosilanes" @default.
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- W2063374352 doi "https://doi.org/10.1021/om8003527" @default.
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