Nucleophilic Iron Catalysis in Transesterifications: Scope and Limitations

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Asymmetric Conjugate Additions of Chiral Phosphonamide Anions to α,β-Unsaturated Carbonyl Compounds. A Versatile Method for Vicinally Substituted Chirons2000 · 42 citations
2. 2No Stirring Necessary: Parallel Carbonylation of Aryl Halides with CO and Various Alcohols under Pressure2003 · 34 citations
3. 3Protecting-Group-Free Synthesis2006 · 283 citations
4. 4Palladium(ii) chloride catalyzed selective acetylation of alcohols with vinyl acetateElectronic supplementary information (ESI) available: 1H, 13C NMR and IR spectral data of 4b, 1H NMR, elemental analysis and IR spectral data of 5b; 1H and IR spectral data of 1b, 2b, 3b, 6b, 7b, 8b, 9b, 11b and 13b. See http://www.rsc.org/suppdata/cc/b4/b401218f/2004 · 38 citations
5. 5Improved Cs2CO3Promoted O-Alkylation of Acids2000 · 21 citations