Alkylation of ethyl bromomalonate by alkylcobaloximes |
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Authors: | M. Veber K.N.V. Duong F. Gaudemer A. Gaudemer |
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Affiliation: | Laboratoire de Chimie de Coordination Bioorganique, CNRS (LA 255) Université Paris-Sud, Centre d''Orsay, 91405 Orsay France |
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Abstract: | ![]() Allylcobaloximes react under very mild conditions with ethyl bromomalonate to yield allyl-substituted ethylmalonates in good yield. In the case of crotyl-, 3,3 dimethyl, allyl- and cinnamyl-cobaloximes, the substitution occurs with total rearrangement of the allyl groups. Similar rearrangements are observed during the reactions of propargyl- and allenylcobaloximes with BrCH(CO2Et)2 yielding allenyl- and propargyl-malonic esters respectively. |
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