| Literature DB >> 19763857 |
Francisco Alonso1, Francisco Foubelo, José C González-Gómez, Ricardo Martínez, Diego J Ramón, Paola Riente, Miguel Yus.
Abstract
A hydrogen autotransfer reaction has been applied to the α-alkylation of ketones, with primary alcohols as the electrophilic component, either under homogeneous (using a Ru complex as catalyst) or under heterogeneous (using Ni nanoparticles) conditions. This process is both very efficient (concerning atom economy) and ecologically friendly (water as the only by-product generated). On the other hand, three multicomponent reactions, namely, the Strecker reaction (without any catalyst), the aza-Sakurai process (catalyzed by ferrite), and the addition of in situ generated Zn enolates to chiral sulfinylimines (catalyzed by Cu), have proven to be very efficient in the generation of a diversity of polyfunctionalized molecules.Entities:
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Year: 2009 PMID: 19763857 DOI: 10.1007/s11030-009-9195-z
Source DB: PubMed Journal: Mol Divers ISSN: 1381-1991 Impact factor: 2.943