Site‐Selective Derivatization and Remodeling of Erythromycin A by Using Simple Peptide‐Based Chiral Catalysts
- 21 August 2006
- journal article
- research article
- Published by Wiley in Angewandte Chemie-International Edition
- Vol. 45 (34), 5616-5619
- https://doi.org/10.1002/anie.200601490
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Lessons from natural moleculesNature, 2004
- Catalytic Enantioselective Synthesis of Sulfinate Esters through the Dynamic Resolution of tert-Butanesulfinyl ChlorideJournal of the American Chemical Society, 2004
- Natural products and combinatorial chemistry: back to the futureCurrent Opinion in Chemical Biology, 2004
- Modern methods to produce natural-product librariesCurrent Opinion in Chemical Biology, 2002
- Discovery of a Catalytic Asymmetric Phosphorylation through Selection of a Minimal Kinase Mimic: A Concise Total Synthesis of d-myo-Inositol-1-PhosphateJournal of the American Chemical Society, 2001
- Selection of Enantioselective Acyl Transfer Catalysts from a Pooled Peptide Library through a Fluorescence-Based Activity Assay: An Approach to Kinetic Resolution of Secondary Alcohols of Broad Structural ScopeJournal of the American Chemical Society, 2001
- Stereochemical Requirements for β-Hairpin Formation: Model Studies with Four-Residue Peptides and DepsipeptidesJournal of the American Chemical Society, 1996
- Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic SynthesisAngewandte Chemie-International Edition, 1985
- Doppelte Stereodifferenzierung und eine neue Strategie zur Stereokontrolle in der Organischen SyntheseAngewandte Chemie, 1985
- Chemical modifications of erythromycin antibiotics. 3. Synthesis of 4'' and 11 esters of erythromycin A and BJournal of Medicinal Chemistry, 1972