A very simple experimental procedure at room temperature allowed to obtain optically active propargyl amines in very good yields and enantioselectivity up to 75%. The extremely simple methodology and the mild reaction conditions, as well as the possibility of a modular approach for developing new and more efficient bis-imine-based chiral ligands make the present methodology very attractive. (c) 2006 Elsevier B.V All rights reserved.

Asymmetric multicomponent copper catalyzed synthesis of chiral propargylamines

Orlandi Simonetta;
2006

Abstract

A very simple experimental procedure at room temperature allowed to obtain optically active propargyl amines in very good yields and enantioselectivity up to 75%. The extremely simple methodology and the mild reaction conditions, as well as the possibility of a modular approach for developing new and more efficient bis-imine-based chiral ligands make the present methodology very attractive. (c) 2006 Elsevier B.V All rights reserved.
2006
multicomponent reactions
chiral copper(I) complexes
asymmetric catalysis
phenylacetylene addition
chiral propargylamines
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/266411
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