Diels–Alder reaction in protic ionic liquids

2006 ◽  
Vol 47 (24) ◽  
pp. 4079-4083 ◽  
Author(s):  
Ewa Janus ◽  
Izabela Goc-Maciejewska ◽  
Marek Łożyński ◽  
Juliusz Pernak
Heterocycles ◽  
2008 ◽  
Vol 76 (1) ◽  
pp. 381 ◽  
Author(s):  
Hiroto Nakano ◽  
Mitsuhiro Takeshita ◽  
Yasuhiro Nishiuchi ◽  
Kouichi Takahashi ◽  
Reiko Fujita ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Vivek Srivastava

Ionic liquids were used to enhance as well as recycle the MacMillan's catalyst1for the Diels-Alder reaction. Using our developed protocol, Diels-Alder adducts were obtained in good yields and selectivities along the 6 times recycling of MacMillan's imidazolidinone catalyst1. Synthesis of steroid4is the major outcome of our developed protocol.


2017 ◽  
Vol 7 (5) ◽  
pp. 1045-1049 ◽  
Author(s):  
K. Matuszek ◽  
S. Coffie ◽  
A. Chrobok ◽  
M. Swadźba-Kwaśny

Ionic liquids with Lewis superacidic borenium cations were used as catalysts in solvent-less Diels–Alder cycloaddition. The extremely high catalytic activity correlated with the Lewis acidity, expressed as the Gutmann acceptor number.


2009 ◽  
Vol 113 (24) ◽  
pp. 8227-8230 ◽  
Author(s):  
Seigo Hayaki ◽  
Kentaro Kido ◽  
Daisuke Yokogawa ◽  
Hirofumi Sato ◽  
Shigeyoshi Sakaki

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.


2005 ◽  
Vol 347 (1) ◽  
pp. 137-142 ◽  
Author(s):  
Donghong Yin ◽  
Changzhi Li ◽  
Biaomo Li ◽  
Liang Tao ◽  
Dulin Yin

2008 ◽  
Vol 73 (22) ◽  
pp. 9075-9083 ◽  
Author(s):  
Shraeddha Tiwari ◽  
Nageshwar Khupse ◽  
Anil Kumar

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