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- W2017222714 abstract "Bis(methylthio)ethene has been shown to undergo Diels–Alder cycloaddition reactions with a range of simple and aryl-fused pyran-2-ones. These reactions can be brought about under either high-temperature or high-pressure conditions. These reactions are all regiospecific and in each case only a single product is isolated, either the initial bridged adduct or an aromatized product generated through decarboxylation. Although this dienophile is less reactive than the corresponding oxygen analogue it is still possible for cycloaddition chemistry to compete effectively with decarboxylation chemistry." @default.
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- W2017222714 date "2010-06-19" @default.
- W2017222714 modified "2023-09-25" @default.
- W2017222714 title "ChemInform Abstract: Diels-Alder Reactions of 1,1-Bis(methylthio)ethene with Pyran-2-ones." @default.
- W2017222714 cites W2951411327 @default.
- W2017222714 doi "https://doi.org/10.1002/chin.199837043" @default.
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