scholarly journals SuFEx-Click Approach for the Synthesis of Soluble Polymer-Bound MacMillan Catalysts for the Asymmetric Diels–Alder Reaction

Catalysts ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 1044
Author(s):  
Woongsup Lee ◽  
Linzi Li ◽  
Byeongmoon Kim

Novel polymeric MacMillan catalysts were prepared from modified chiral imidazolidin-4-one monomers via sulfur(VI) fluoride exchange chemistry. The resulting polysulfates containing chiral imidazolidin-4-one units could be employed as polymeric organocatalysts for the asymmetric Diels–Alder reaction. With the use of these polysulfate catalysts, sufficient catalytic activity and enantioselectivity were obtained, which were similar to those obtained by monomeric catalysts in a homogeneous catalytic reaction. In addition, the polysulfate catalysts could be recovered and reused five times without a considerable loss of activity and selectivity.

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.


1997 ◽  
Vol 75 (8) ◽  
pp. 1047-1054 ◽  
Author(s):  
Claude Spino ◽  
Laurel L. Clouston ◽  
David J. Berg

A series of yttrium, ytterbium, and lanthanum hexa-or heptacoordinate complexes were prepared and their catalytic activities tested in the hetero Diels–Alder reaction between crotonaldehyde and ethyl vinyl ether. It was found that a pKa below 7 of the ligand was necessary but not sufficient for catalytic activity. It was determined that the ligand should possess a perfluoromethyl-β-diketonate functionality. Other factors such as bite angle and hinging motion may also play a determining role. Keywords: lanthanide, catalyst, hetero Dielsis–Alder, yttrium, ytterbium, lanthanum.


2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Carlos A. D. Sousa ◽  
José E. Rodríguez-Borges ◽  
Cristina Freire

New L-serine derivative ligands were prepared and tested as cocatalyst in the Diels-Alder reactions between cyclopentadiene (CPD) and methyl acrylate, in the presence of several Lewis acids. The catalytic potential of the in situ formed complexes was evaluated based on the reaction yield. Bidentate serine ligands showed good ability to coordinate medium strength Lewis acids, thus boosting their catalytic activity. The synthesis of the L-serine ligands proved to be highly efficient and straightforward.


ChemInform ◽  
2004 ◽  
Vol 35 (11) ◽  
Author(s):  
Choji Kashima ◽  
Saori Shibata ◽  
Hiroyo Yokoyama ◽  
Takehiko Nishio

2014 ◽  
Vol 79 (18) ◽  
pp. 8684-8688 ◽  
Author(s):  
Bastien Chatelet ◽  
Véronique Dufaud ◽  
Jean-Pierre Dutasta ◽  
Alexandre Martinez

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