Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10572838 | Journal of Fluorine Chemistry | 2005 | 8 Pages |
Abstract
The reaction of β-ethoxyvinyl trifluoromethyl ketone 1 with O-nucleophiles such as alcohols and diols leads to various derivatives of trifluoroacetyl acetaldehyde, such as β-alkoxyvinyl trifluoromethyl ketones 3 and cyclic keto acetals 4. Several derivatives synthesized contain chiral auxiliaries. Reduction of the compounds 1, 3, 4 under various reaction conditions leads to the trifluoroaldol derivatives 6, 7, 9, 10 containing a protected aldehyde group. The compounds obtained are useful building blocks in fluoroorganic synthesis.
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Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Ivan S. Kondratov, Igor I. Gerus, Aleksey D. Kacharov, Marina G. Gorbunova, Valery P. Kukhar, Roland Fröhlich,