Stereoselective synthesis of erythro-β-hydroxy carboxylic acids via iron acyl complexes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. 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)
2. 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}]
3. S.G. Davies and J.I. Seeman, Tetrahedron Letters, in press.
4. Chemistry of dicarbonyl .eta.5-cyclopentadienyliron complexes. General syntheses of monosubstituted .eta.2-olefin complexes and of 1-substituted .eta.1-allyl complexes. Conformational effects on the course of deprotonation of (.eta.2-olefin) cations
5. Elaboration of acyl ligands: Preparation and reactivity of the anion [(η5-C5,H5)Fe(CO)(PPh3)(COCH2)]−
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