K2CO3‐ oder Cs2CO3‐katalysierte diastereoselektive Drei‐Zentren‐Michael‐Addition von β‐Ketoestern an prostereogene α,β ungesättigte Carbonylverbindungen
- 1 December 1992
- journal article
- Published by Wiley in Angewandte Chemie
- Vol. 104 (12) , 1658-1660
- https://doi.org/10.1002/ange.19921041226
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Total synthesis of (+)-griseofulvinJournal of the American Chemical Society, 1991
- Acyclic Stereocontrol in Michael Addition Reactions of Enamines and Enol EthersPublished by Wiley ,1991
- Prelog-Djerassi Lactonic Acid. A Target for Design and Development of Stereoselective Synthetic MethodsSynthesis, 1991
- Triple ion chelate structure of an equilibrium Michael adductJournal of Physical Organic Chemistry, 1990
- The anti-selective Michael addition of allylic organometals to ethylidenemalonates and related compoundsThe Journal of Organic Chemistry, 1988
- Acyclic stereoselection. 31. Stereoselection in the Michael addition reaction. 3. Relationship between ester enolate geometry and adduct stereochemistry in the kinetic Michael reaction of lithium enolates with enonesThe Journal of Organic Chemistry, 1985
- Spezifikation des sterischen Verlaufs von asymmetrischen SynthesenAngewandte Chemie, 1982
- The Unambiguous Specification of the Steric Course of Asymmetric SynthesesAngewandte Chemie International Edition in English, 1982
- A Facile Alkylation of Ethyl 2-OxocyclopentanecarboxylateSynthesis, 1973
- Chemistry of cephlosporin antibiotics. XVIII. Synthesis of 7-acyl-3-methyl-2-cephem-4-carboxylic acid estersThe Journal of Organic Chemistry, 1970