A peptide-catalyzed asymmetric Stetter reaction
Chemical Communications2004Iss. 2, pp. 195–197
Citations Over TimeTop 10% of 2004 papers
Abstract
Thiazolylalanine, in appropriately functionalized form, has been found to function as an enantioselective catalyst for an intramolecular Stetter reaction. Incorporation of the residue in a number of environments has resulted in a family of catalysts that promote the cyclization of a test substrate with up to 81% enantiomeric excess.
Related Papers
- → Enantiomeric enrichment of non-racemic mixtures of binaphthol with non-chiral packings(1996)47 cited
- → Enantiomeric enrichment by the use of density differences between racemic compounds and optically active enantiomers(1995)16 cited
- → Resolution of Optical Isomers by Thin‐Layer Chromatography: Enantiomeric Purity of Methyldopa. Dünnschichtchromatographische Enantiomerentrennung: Enantiomere Reinheit von Methyldopa(1986)43 cited
- → Highly enantioselective asymmetric autocatalysis of 2‐alkenyl‐ and 2‐vinyl‐5‐pyrimidyl alkanols with significant amplification of enantiomeric excess(2002)31 cited
- → Colour indicator for enantiomeric excess and assignment of the configuration of the major enantiomer of an amino acid ester(2002)26 cited