Monatshefte fur Chemie p. 1133 - 1140 (1985)
Update date:2022-08-02
Topics: Ester Nucleophilic substitution Cyclic voltammetry Substituted Product Isolation Electrochemical Cell Electrolysis Spectroscopic Analysis Anode Cathode Oxidation state Mechanistic study Radical intermediate Controlled Potential Electrolysis Faradaic Efficiency
Knittel, Dierk
Several ring-substituted α-azidocinnamic and β-heterocyclic α-azidoacrylic esters are subject to cathodic reduction under aprotic and protic conditions.Good to excellent yields of rather labile dehydroaminoacid derivatives resp. stable N,N-diacylated enam
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Doi:10.1021/jo00363a004
(1986)Doi:10.1016/j.tetasy.2008.02.005
(2008)Doi:10.1021/ja01520a009
(1959)Doi:10.1039/c7dt04287f
(2018)Doi:10.1016/j.bmcl.2008.01.086
(2008)Doi:10.1016/0022-5088(86)90229-8
(1986)
