With Metal Salt Based Lewis Acid Catalysts

Author(s):  
T. Takeda ◽  
A. Tsubouchi
2015 ◽  
Vol 39 (12) ◽  
pp. 9824-9833 ◽  
Author(s):  
Babita Tanwar ◽  
Dinesh Kumar ◽  
Asim Kumar ◽  
Md. Imam Ansari ◽  
Mohammad Mohsin Qadri ◽  
...  

In(OTf)3 is the most effective catalyst among metal halides, tetrafluoroborates, perchlorates, and triflates for Friedländer quinoline synthesis in 75–92% yields.


ChemInform ◽  
2016 ◽  
Vol 47 (14) ◽  
Author(s):  
Babita Tanwar ◽  
Dinesh Kumar ◽  
Asim Kumar ◽  
Md. Imam Ansari ◽  
Mohammad Mohsin Qadri ◽  
...  

2018 ◽  
Vol 5 (11) ◽  
pp. 2763-2771 ◽  
Author(s):  
Hao Xu ◽  
Xudong Wang ◽  
Peng Ji ◽  
Haihong Wu ◽  
Yejun Guan ◽  
...  

Sn-Beta zeolites, with high Sn content and smaller crystal size, hydrothermally synthesized in F−-free medium using N-cyclohexyl-N,N-dimethylcyclohexanaminium hydroxide as the structure-directing agent with the assistance of Na+ and seed, are highly active as Lewis acid catalysts.


2003 ◽  
Vol 17 (10) ◽  
pp. 795-799 ◽  
Author(s):  
Yasuo Imakura ◽  
Satoru Nishiguchi ◽  
Akihiro Orita ◽  
Junzo Otera

ChemInform ◽  
2013 ◽  
Vol 44 (40) ◽  
pp. no-no
Author(s):  
Jeanne-Marie Begouin ◽  
Meike Niggemann

1975 ◽  
Vol 53 (4) ◽  
pp. 616-618 ◽  
Author(s):  
Žarko Stojanac ◽  
Robert A. Dickinson ◽  
Nada Stojanac ◽  
Ronald J. Woznow ◽  
Zdenek Valenta

Lewis acid catalysts cause an orientation reversal in the Diels–Alder additions of 2,6-di-methyl-1,4-quinone (1) and toluquinone (12) to 1-substituted 1,3-butadienes and to 1,2- and 1,3-dialkyl dienes. These results are explained by the preferential formation of one reactive quinone–Lewis acid salt.


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