scholarly journals A theoretical study of the solvent effect on Diels-Alder reaction in room temperature ionic liquids using a supermolecular approach

2009 ◽  
Vol 123 (3-4) ◽  
pp. 347-352 ◽  
Author(s):  
Riccardo Bini ◽  
Cinzia Chiappe ◽  
Veronica L. Mestre ◽  
Christian S. Pomelli ◽  
Thomas Welton
2007 ◽  
Vol 20 (2) ◽  
pp. 109-114 ◽  
Author(s):  
Ana Vidiš ◽  
Gábor Laurenczy ◽  
Ernst Küsters ◽  
Gottfried Sedelmeier ◽  
Paul J. Dyson

2005 ◽  
Vol 347 (2-3) ◽  
pp. 266-274 ◽  
Author(s):  
Ana Vidiš ◽  
C. André Ohlin ◽  
Gábor Laurenczy ◽  
Ernst Küsters ◽  
Gottfried Sedelmeier ◽  
...  

2010 ◽  
Vol 8 (2) ◽  
pp. 356-360 ◽  
Author(s):  
Nitin Mirgane ◽  
Sandip Kotwal ◽  
Anil Karnik

AbstractIonic liquids (IL) are gaining importance as green solvents. Imidazolium ionic liquid [bmim]+[Cl]−, an environmentally benign solvent, was found to promote the Diels-Alder reaction between anthrone and maleimides at room temperature with excellent yields. The ionic liquid played a dual role as solvent and catalyst.


2015 ◽  
Vol 11 ◽  
pp. 576-582 ◽  
Author(s):  
Grzegorz Mlostoń ◽  
Paulina Grzelak ◽  
Maciej Mikina ◽  
Anthony Linden ◽  
Heinz Heimgartner

Selected hetaryl and aryl thioketones react with acetylenecarboxylates under thermal conditions in the presence of LiClO4 or, alternatively, under high-pressure conditions (5 kbar) at room temperature yielding thiopyran derivatives. The hetero-Diels–Alder reaction occurs in a chemo- and regioselective manner. The initially formed [4 + 2] cycloadducts rearrange via a 1,3-hydrogen shift sequence to give the final products. The latter were smoothly oxidized by treatment with mCPBA to the corresponding sulfones.


1983 ◽  
Vol 93 ◽  
pp. 255-260 ◽  
Author(s):  
L. Pardo ◽  
V. Branchadell ◽  
A. Oliva ◽  
J. Bertrán

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