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Phosphorylation of Conjugated Enamines
Authors:Aleksandr N. Kostyuk  Nikolai V. Lysenko  Sergei I. Dovgopoly  Andrei A. Tolmachev
Affiliation:Institute of Organic Chemistry, National Academy of Sciences of Ukraine , Murmanskay str. 5 253660, Kiev , 94 , UKRAINE
Abstract:Abstract

Introduction of benzylidene group at α-position of enamines derived from cyclic ketones substantially increases strength of C-P bond thus permitting further syntheses without splitting of the C-P bond. A wide set of phosphorylated derivatives of type (I) were prepared and their properties were studied. Combination of an enamine moiety with other nucleophilic centers such as C or N in a molecule allows to carry out cyclisation giving five- and six-membered phosphorus-containing heterocycles of types (II, III).
Keywords:
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