Diastereoselective Coupling of 1,3-Diene, Ketone, and Organometallic Reagents by Nickel Catalyst: Stereoselective Construction of Tetrasubstituted Carbon Centers-Reference-Cited by-同舟云学术

Diastereoselective Coupling of 1,3-Diene, Ketone, and Organometallic Reagents by Nickel Catalyst: Stereoselective Construction of Tetrasubstituted Carbon Centers

Published:2009-06-05 Issue:6 Volume:38 Page:594-595
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Saito Nozomi,Yamazaki Tetsuro,Sato Yoshihiro

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference31 articles.

1. Asymmetric Multicomponent Reactions (AMCRs): The New Frontier

2. Nickel-catalyzed regio- and stereoselective synthesis of homoallylic alcohol derivatives from dienes and aldehydes

3. Dramatic Influence on the Olefinic Geometry in the Nickel(0)-Catalyzed Coupling Reaction of 1,3-Dienes and Aldehydes Using N-Heterocyclic Carbene as a Ligand

4. Ligand-Controlled Highly Stereoselective Syntheses of E- and Z-Allylsilanes from Dienes and Aldehydes Using Nickel Complex

5. Nickel-Catalyzed Enantio- and Diastereoselective Three-Component Coupling of 1,3-Dienes, Aldehydes, and Silanes Using Chiral N-Heterocyclic Carbenes as Ligands

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