2004
DOI: 10.1016/j.jfluchem.2003.10.010
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One step synthesis of 2-substituted 3-tri-(or di-)fluoromethyl-2-propenals in an ionic liquid

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Cited by 8 publications
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“…In 2004, Kitazume et al [ 74 ] elaborated a one-stage synthesis of 2-substituted 3-tri-(or di-)-fluoromethyl-2-propenals using versatile aldehydes, tri- or di-fluoroacetaldehyde ethyl hemiacetal in the presence of diethylaminotrimethylsilane (DEATMS) in an ionic liquid. This protocol permits us to successfully construct 2-substituted propenals with high levels of selectivity of the geometric isomers ( Scheme 23 ).…”
Section: Synthesis Of α-Functionally Substituted αβ-Unsaturated Aldehydesmentioning
confidence: 99%
“…In 2004, Kitazume et al [ 74 ] elaborated a one-stage synthesis of 2-substituted 3-tri-(or di-)-fluoromethyl-2-propenals using versatile aldehydes, tri- or di-fluoroacetaldehyde ethyl hemiacetal in the presence of diethylaminotrimethylsilane (DEATMS) in an ionic liquid. This protocol permits us to successfully construct 2-substituted propenals with high levels of selectivity of the geometric isomers ( Scheme 23 ).…”
Section: Synthesis Of α-Functionally Substituted αβ-Unsaturated Aldehydesmentioning
confidence: 99%