β-Homoamino acids as catalysts in enantioselective intra- and intermolecular aldol reactions |
| |
Authors: | Michael Limbach |
| |
Institution: | Laboratorium für Organische Chemie, Department Chemie und Angewandte Biowissenschaften, Eidgenössische Technische Hochschule, ETH Hönggerberg, HCI, Wolfgang-Pauli-Strasse 10, CH-8093 Zürich, Switzerland |
| |
Abstract: | β3-Homoamino acids catalyze the intra- (cf. the Hajos-Parrish-Eder-Sauer-Wiechert reaction) as well as the intermolecular aldol reaction. The stereochemical outcome with selectivities of up to 83% ee is reversed in the intramolecular reaction, when we go from the proteinogenic amino acids to the homologues, and reaction time increases dramatically for both reactions. In contrast, in the intermolecular reaction Me-β3hPhe-OH gives the same enantiomer as (S)-proline does, but with lower enantiomeric excess (54% vs 48% ee). |
| |
Keywords: | |
本文献已被 ScienceDirect 等数据库收录! |
|