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Synthesis 2016; 48(17): 2768-2780
DOI: 10.1055/s-0035-1562103
DOI: 10.1055/s-0035-1562103
special topic
Asymmetric Catalysis with Iron–Salen Complexes
Further Information
Publication History
Received: 13 March 2016
Accepted after revision: 04 April 2016
Publication Date:
23 May 2016 (online)
Abstract
Iron(III)–salen complexes based on a chiral cis-2,5-diaminobicyclo[2.2.2]octane scaffold are used as catalysts for a variety of stereoselective reactions. High enantio- and diastereoselectivities can be achieved with these catalysts in sulfa-Michael conjugate addition to acyclic α,β-unsaturated ketones, in regioselective δ-addition of thiols to acyclic α,β,γ,δ-unsaturated ketones, and in Conia-ene carbocyclization of alkynyl-substituted β-dicarbonyl compounds. The use of these chiral iron–salen complexes as catalysts provides a new method for conducting these three important reactions under environmentally sustainable conditions.
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For selected examples of Fe-catalyzed transfer hydrogenation, see:
For selected examples of preferential 1,4- over 1,6-conjugate additions to α,β,γ,δ-unsaturated carbonyl systems, see: