STEREOSELECTIVITY OF THE REACTION OF MERCURIC ACETATE WITH DIMETHYL BICYCLO[2.2.2]OCT-2-EN-5,6-CIS-ENDO-DICARBOXYLATEстатья
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Дата последнего поиска статьи во внешних источниках: 18 июля 2013 г.
Аннотация:The stereoselelectivity of the reaction of mercuric acetate with dimethyl bicyclo[2.2.2]oct-2-en-5,6-cis-endo-carboxylate in acetic acid was studied. One of the reaction products is formed when the reagent attacks the double bond from the sterically less accessible side. The nature of the orientation effect of the carboxylate groups is discussed.