Electrochemical transformation of alkylidenemalonates into 2-alkyl-3,3-dimethoxyalkane-1,1-dicarboxylates via rearrangement
摘要:
Alkylidenemalonates capable of migration of a double bond being electrolyzed in methanol in the presence of alkali metal halides in an undivided cell are transformed into 2-alkyl-3,3-dimethoxyalkane-1,1-dicarboxylates, acidification of which leads to 2-alkyl-3-oxoalkane-1,1-dicarboxylates.
Electrochemical cyclodimerization of alkylidenemalonates
作者:Michail N. Elinson、Sergey K. Feducovich、Alexandre A. Zakharenkov、Bogdan I. Ugrak、Gennady I. Nikishin、Sergey V. Lindeman、Jurii T. Struchkov
DOI:10.1016/0040-4020(95)98700-r
日期:1995.4
in MeOH in the presence of alkalimetalhalide as mediator, leads to the formation of cyclic dimers, i.e., 3,4-disubstituted 1,1,2,2-cyclobutanetetracarboxylates. The reaction proceeds via the reductive coupling of two substrate molecules at cathode and the cyclization of a hydrodimer dianion by its interaction with an active form of a mediator, an anode-generated halogen.
Electrochemically induced oxidative rearrangement of alkylidenemalonates
作者:Michail N Elinson、Sergey K Feducovich、Gennady I Nikishin
DOI:10.1016/s0040-4020(98)00912-0
日期:1998.11
Alkylidenemalonates capable of double bond migration being electrolyzed in methanol or ethanol in the presence of alkali metal halides in an undivided cell equipped with Fe cathode are transformed into 2-alkyl-3,3-dimethoxyalkane-1,1-dicarboxylates in 70-90% yield via electrochemically induced oxidative rearrangement. Acidification of the reaction mixture after the electrolysis leads to the formation of 2-alkyl-3-oxoalkane-1,1-dicarboxylates. In the case of isobutylidenemalonate, the electrolysis intermediate dimethyl 3,3-dimethyl-2-methoxycyclopropane-1,1-dicarboxylate was isolated in 70% yield. (C) 1998 Published by Elsevier Science Ltd. All rights reserved.
Ketene thioacetal monoxides: A novel and versatile class of two-carbon michael receptors
Electrochemical cyclodimerization of alkylidenemalonates into 3,4-disubstituted cyclobutane-1,1,2,2-tetracarboxylates
作者:Gennady I. Nikishin、Michail N. Elinson、Sergey K. Feducovich、Bogdan I. Ugrak、Yuri T. Struchkov、Sergey V. Lindeman
DOI:10.1016/s0040-4039(00)79857-1
日期:1992.5
Alkylidenemalonates being electrolyzed in methanol in undivided cell with glassy carbon, carbon or lead cathode in the presence of sodium iodide or sodium bromide are transformed into 3,4-disubstituted cyclobutane-1,1,2,2-tetracarboxylates.