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- W2952652117 abstract "Normal, neutral, and inverse-type Diels–Alder reactions can be observed in [4+2] cycloadditions of thio- and selenocarbonyl compounds 1–9 with various cyclic and aryl-, methyl- or methoxy-substituted open-chain 1,3-butadienes. Extensive kinetic studies prove the highly dienophilic activity of the CS and CSe double bond. Studies of the solvent and temperature dependence of the reaction rate indicate a concerted mechanism." @default.
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- W2952652117 date "2010-06-16" @default.
- W2952652117 modified "2023-09-25" @default.
- W2952652117 title "ChemInform Abstract: Thio- and Selenocarbonyl Compounds as “Superdienophiles” in [4 + 2] Cycloadditions." @default.
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- W2952652117 doi "https://doi.org/10.1002/chin.199916057" @default.
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