Diastereo‐ und enantioselektive Synthese 1,2‐trans‐substituierter Cycloalkancarbonsäureester und Sulfone durch Michael‐initiierte Cyclisierungen via SAMP‐/RAMP‐Hydrazone[1,2]
- 1 August 1993
- journal article
- research article
- Published by Wiley in European Journal of Inorganic Chemistry
- Vol. 126 (8), 1929-1944
- https://doi.org/10.1002/cber.19931260825
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- Diastereo‐ and Enantioselective Michael Addition Initiated Cyclizations to trans‐Substituted CyclopentanecarboxylatesAngewandte Chemie International Edition in English, 1991
- Annulation Reactions ofOrtho-Chloromethyl Aryl CupratesSynthetic Communications, 1990
- Oxidative Cleavage ofN,N-Dialkylhydrazones to Ketones with Magnesium MonoperoxyphthalateSynlett, 1990
- MICHAEL ADDITION OF ORGANOLITHIUM COMPOUNDS. A REVIEWOrganic Preparations and Procedures International, 1989
- Anionic approaches to the construction of cyclopentanoidsChemical Reviews, 1989
- Asymmetric Michael Additions via SAMP‐/RAMP‐Hydrazones Enantioselective 1,4‐Addition of Methyl Ketones to Knoevenagel Acceptors1)European Journal of Inorganic Chemistry, 1987
- Asymmetric Michael Additions via SAMP‐/RAMP‐Hydrazones Enantioselective Synthesis of β‐Substituted Δ‐Oxopentanoates and δ‐Lactones1)European Journal of Inorganic Chemistry, 1987
- Improved route to 3-vinyl substituted cyclopentanones. Synthesis of (.+-.)-mitsugashiwalactoneThe Journal of Organic Chemistry, 1986
- Fünfgliedrige Ringe durch [3+2]‐Cycloaddition mit Trimethylenmethan und SyntheseäquivalentenAngewandte Chemie, 1986
- A regiospecific, convergent route to 2,3-disubstituted cyclopentanonesThe Journal of Organic Chemistry, 1983