Addition of electrochemically-generated anions to aldehydes and olefins: effect of reaction medium and anion basicity
- 31 December 1997
- journal article
- Published by Elsevier in Electrochimica Acta
- Vol. 42 (13-14) , 2247-2255
- https://doi.org/10.1016/s0013-4686(97)85506-5
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Cathodically promoted highly selective Michael addition of nitro compounds to levoglucosenone.Tetrahedron Letters, 1993
- Oxidation potential as a measure of the effect of environment on the reactivity of anionic nucleophilesJournal of the Chemical Society, Perkin Transactions 2, 1993
- Electrogeneration of the anion of ethyl nitroacetate and its use in electroorganic synthesisThe Journal of Organic Chemistry, 1993
- Water-promoted organic reactions. Michael addition of nitroalkanes to methylvinylketone under neutral conditionsTetrahedron Letters, 1992
- Inter- and intramolecular [4 + 2] cycloadditions of nitroalkenes with olefins. 2-NitrostyrenesThe Journal of Organic Chemistry, 1992
- Starburst Dendrimers: Molecular‐Level Control of Size, Shape, Surface Chemistry, Topology, and Flexibility from Atoms to Macroscopic MatterAngewandte Chemie International Edition in English, 1990
- Equilibrium acidities in dimethyl sulfoxide solutionAccounts of Chemical Research, 1988
- Equilibrium acidities of carbon acidsPure and Applied Chemistry, 1977
- Recent Developments in NitroparaffinsIndustrial & Engineering Chemistry, 1943
- 126. The effect of the nitro-group in three-carbon tautomerismJournal of the Chemical Society, 1934