Chiral discrimination in the reactions of the enolate E-[(η5-C5H5)Fe(CO)(PPh3)COCHMe]−Li+ with and but-2-ene oxides in the presence of BF3·OEt3
- 1 January 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (39) , 4815-4818
- https://doi.org/10.1016/s0040-4039(00)94959-1
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Chiral propionate enolate equivalent for stereoselective additions to symmetrical ketonesTetrahedron Letters, 1985
- Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic SynthesisAngewandte Chemie International Edition in English, 1985
- Chiral propionate enolate equivalents for the stereoselective synthesis of threo- or erytho-α,-methyl-β-hydroxy acidsTetrahedron Letters, 1985
- Stereoselective synthesis of erythro-β-hydroxy carboxylic acids via iron acyl complexesTetrahedron Letters, 1984
- Rules governing asymmetric synthesis with organotransition metal complexesTetrahedron Letters, 1984
- Stereoselective elaboration of the acyl ligand in (η5-C5H5)Fe(CO)(PPh3)(COCH2R) via the alkylation of the anions [(η5-C5H5)Fe(CO)(PPh3)(COCHR)]Li (R = Me, Et)Journal of Organometallic Chemistry, 1983
- Stereochemical control and mechanistic aspects of the alkylation of [(η5-C5H5)Fe(L)(CO)(COCHR)]–Li+(L = PPh3, PPh2NEt2; R = Me, Et): X-ray crystal structure of [(η5-C6H5)Fe(PPh3)(CO){COCH(Me)Et}]Journal of the Chemical Society, Chemical Communications, 1983
- α‐Chlor‐nitrone IV: Zur Stereochemie der λ‐Lacton‐Synthese und eine Methode zum Aufbau von α‐Methyliden‐λ‐lactonen aus Olefinen. Über synthetische Methoden, 8. (vorläufige) MitteilungHelvetica Chimica Acta, 1973