Unexpected chemoselectivity in the rhodium-catalyzed transfer hydrogenation of α,β-unsaturated ketones in ionic liquids

2009 ◽  
Vol 11 (12) ◽  
pp. 1937 ◽  
Author(s):  
Zoltán Baán ◽  
Zoltán Finta ◽  
György Keglevich ◽  
István Hermecz
2016 ◽  
Vol 81 (9) ◽  
pp. 3528-3532 ◽  
Author(s):  
Scott A. Van Arman ◽  
Austin J. Zimmet ◽  
Ian E. Murray

2007 ◽  
Vol 79 (11) ◽  
pp. 1869-1877 ◽  
Author(s):  
Anthony E. Rosamilia ◽  
Christopher R. Strauss ◽  
Janet L. Scott

Adducts of dimethylamine and carbon dioxide form a "distillable ionic liquid" (DIMCARB) that may used as both a reaction medium and catalyst in the direct, atom-economical synthesis of useful synthetic building blocks, such as mono-condensed α,β-unsaturated ketones. The utilization of such building blocks in the synthesis of two new classes of versatile macrocycles, by a sequence of condensation reactions (H2O by-product), is described. Investigation into the mechanism of action of DIMCARB catalysis and observation of an aniline impurity arising from a competing reaction sequence led to development of a new multicomponent reaction for the direct preparation of 2- or 4-substituted anilines. Some of the macrocycles and anilines are, respectively, supramolecular host compounds and ligands for the preparation of metal complexes.


Tetrahedron ◽  
2005 ◽  
Vol 61 (40) ◽  
pp. 9541-9544 ◽  
Author(s):  
J.S. Yadav ◽  
B.V. S. Reddy ◽  
Gakul Baishya ◽  
K.V. Reddy ◽  
A.V. Narsaiah

ARKIVOC ◽  
2006 ◽  
Vol 2006 (4) ◽  
pp. 152-160 ◽  
Author(s):  
Jean-Michel Joerger ◽  
Jean-Marc Paris ◽  
Michel Vaultier

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