Über den sterischen Verlauf der Umsetzung von Enaminen aus offenkettigen Aldehyden und Ketonen mit Nitroolefinen zu 2,3‐disubstituierten 4‐Nitroketonen
- 13 February 1985
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 68 (1), 162-172
- https://doi.org/10.1002/hlca.19850680120
Abstract
No abstract availableKeywords
This publication has 54 references indexed in Scilit:
- Acyclic stereoselection. 21. Synthesis of an ionophore synthon having four asymmetric carbons by sequential aldol addition, claisen rearrangement and hydroborationTetrahedron Letters, 1984
- The Aldol Addition ReactionPublished by Elsevier ,1984
- Basic Principles of the CIP‐System and Proposals for a RevisionAngewandte Chemie International Edition in English, 1982
- Grundlagen des CIP-Systems und Vorschläge für eine RevisionAngewandte Chemie, 1982
- Synthesis of Open‐Chain 2,3‐Disubstituted 4‐nitroketones by Diastereoselective Michael‐addition of (E)‐Enamines to (E)‐Nitroolefins. A topological rule for C, C‐bond forming processes between prochiral centres. Preliminary communicationHelvetica Chimica Acta, 1981
- Acyclic stereoselection. 2. Synthesis of 3-hydroxy-2-methyl- and 3-hydroxy-2,4-dimethylcarboxylic acidsJournal of the American Chemical Society, 1977
- The crystal and molecular structure of the adduct from the diastereoisomeric equilibrium mixture of racemic 2-(α-phenyl-β-nitro)ethyl-4-tert-butyl-cyclohexanoneTetrahedron, 1975
- Vinylamines—XVTetrahedron, 1974
- Vinylamines—XIVTetrahedron, 1973
- Vinylamines—VIIITetrahedron, 1968