| Literature DB >> 29710956 |
Takashi Ooi1, Tomoya Miura1, Keiji Maruoka1.
Abstract
Double electrophilic activation of carbonyl groups allows a modern variant of the Meerwein-Ponndorf-Verley reduction to be carried out under mild conditions with bidentate catalyst 1 (see reaction). Various carbonyl substrates can be reduced efficiently at room temperature in CH2 Cl2 with 2-propanol or sec-phenethyl alcohol in the presence of a catalytic amount of 1. This system is also applicable to the Oppenauer oxidation of secondary alcohols to the corresponding ketones. © 1998 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany.Entities:
Keywords: Aluminum; Asymmetric synthesis; Homogeneous catalysis; Oxidations; Reductions
Year: 1998 PMID: 29710956 DOI: 10.1002/(SICI)1521-3773(19980918)37:17<2347::AID-ANIE2347>3.0.CO;2-U
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336