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Free-radical reactions of methyl trifluoropyruvate with aldehydes
Authors:E. A. Markova  A. F. Kolomiets  A. V. Fokin
Affiliation:(1) A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813 Moscow, Russian Federation
Abstract:Methyl trifluoropyruvate reacts with aldehydes in the presence of catalytic amounts of benzoyl peroxide at 130–140°C to give β,β,β-trifluoro-α-(methoxycarbonyl)ethyl carboxylates. UV irradiation makes oligomerization of the initial ketoester predominant. Deceased. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1763–1766, September, 1998.
Keywords:methyl trifluoropyruvate, reaction with aldehydes  benzoyl peroxide  UV irradiation  free-radical reactions  β      -trifluoro-α  -(methoxycarbonyl)ethyl carboxylates, synthesis
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