Transition-Metal-MediatedExo-Selective Diels−Alder Reactions for the Preparation of Octalones with Unusual Stereochemistries. Reactions of 2-Cobaloxime-Substituted 1,3-Dienes with Cyclohexenones in Thermal and Lewis Acid-Catalyzed [4 + 2] Cycloadditions

1997 ◽  
Vol 62 (5) ◽  
pp. 1299-1304 ◽  
Author(s):  
B. Matthew Richardson ◽  
Mark E. Welker

2008 ◽  
Vol 80 (5) ◽  
pp. 1013-1018 ◽  
Author(s):  
Andrei Bădoiu ◽  
Yasmin Brinkmann ◽  
Florian Viton ◽  
E. Peter Kündig

Highly tuned, one-point binding chiral iron and ruthenium complexes selectively coordinate and activate α,β-unsaturated aldehydes and ketones toward asymmetric catalytic Diels-Alder cycloaddition reactions. Here we focus on the application of these transition-metal Lewis acids to asymmetric catalytic 1,3-dipolar cycloaddition reaction between enals and cyclic and acyclic nitrones as well as aryl nitrile oxides to give isoxazolidines and isoxazolines, respectively.







2000 ◽  
Vol 11 (12) ◽  
pp. 2509-2523 ◽  
Author(s):  
Renée Paugam ◽  
Emmanuelle Valenciennes ◽  
Linda Le Coz-Bardol ◽  
Jean-Christophe Garde ◽  
Lya Wartski ◽  
...  


ChemInform ◽  
2010 ◽  
Vol 33 (11) ◽  
pp. no-no
Author(s):  
Colin A. Ray ◽  
Erik Risberg ◽  
Peter Somfai




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