Showing papers by "Yu. N. Ogibin published in 1971"
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TL;DR: In this paper, the α-carbon atom of the alcohol portion of the ester molecule takes part either exclusively or predominantly in the formation of the new carbon bond of the adducts.
Abstract: 1.
A study was made of the addition reaction, initiated by peroxides, of diethyl malonate, dimethyl succinate and ethyl monochloroacetate to the polyhaloolefins — to hexafluoropropylene, trichloroethylene and tetrachloroethylene.
2.
The reaction proceeds by an anomalous direction: the α-carbon atom of the alcohol portion of the ester molecule takes part either exclusively or predominantly in the formation of the new carbon — carbon bond of the adducts.
3.
The reaction of esters with trichloro- and tetrachloroethylene is accompanied by the elimination of hydrogen chloride and leads to the respective formation of either the 1-(dichlorovinyl) or 1-(trichlorovinyl) derivatives of alkyl esters of carboxylic acids.
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