Chiral dienolates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference34 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. Improved stereochemical control and mechanistic aspects of the alkylation of enolates derived from [(η5-C5H5)Fe(CO)(PPh3)COCH2R]
4. Stereoselective synthesis of erythro-β-hydroxy carboxylic acids via iron acyl complexes
5. Chiral acetate enolate equivalent for the synthesis of β-hydroxy acids
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1. Mutual kinetic resolution: probing enantiorecognition phenomena and screening for kinetic resolution with racemic reagents;Organic & Biomolecular Chemistry;2021
2. Metal-Mediated, Carbon-Carbon Bond-Forming Reactions;Organic Synthesis;2017
3. Stereoselective syntheses of substituted succinic acid derivatives of the iron chiral auxiliary [(η5-C5H5)Fe(CO)(PPh3)];Tetrahedron;2014-11
4. Stereochemical aspects of nucleophilic addition reactions to alkoxycarbene cations of the iron chiral auxiliary [(η5-C5H5)Fe(CO)(PPh3)];New Journal of Chemistry;2013
5. Optically active transition-metal complexes. 104. Asymmetric Michael reactions of iron complexes (RFe)- and (SFe)-[(.eta.5-C5H5)Fe(CO)(PPh3)COCH:CH2]. Synthesis of an enantiomerically pure precursor for verapamil. X-ray crystal structure of [RFeRC)-{(.eta.5-C5H5)Fe(CO)(PPh3)COCH2CH2C(CN)(iPr)[3,4-C6H3(OMe)2]};Organometallics;1993-10
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