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- W2078875894 abstract "Selenothioic acid S-alkyl esters were reacted with allylic bromides in the presence of Et3N. Mono-, di- or tri-allylatd products were selectively formed by changing reaction temperatures, times and allylic bromides used. The reaction proceeded with high regio- and stereoselectivity via the seleno-Claisen rearrangement. The selective synthesis of monoallylated esters was also attained by the reaction of in-situ generated lithium eneselenolates with allylic bromides." @default.
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- W2078875894 date "1997-08-01" @default.
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- W2078875894 title "4-Penteneselenothioic acid S-alkyl esters: Synthesis via the seleno-Claisen rearrangement" @default.
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- W2078875894 doi "https://doi.org/10.1016/s0040-4020(97)00556-5" @default.
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