Acidity dependence of the trifluoromethanesulfonic acid catalyzed isobutane-isobutylene alkylation modified with trifluoroacetic acid or water

1996 ◽  
Vol 146 (1) ◽  
pp. 107-117 ◽  
Author(s):  
George A. Olah ◽  
Patrice Batamack ◽  
Denis Deffieux ◽  
Béla Török ◽  
Qi Wang ◽  
...  
1957 ◽  
Vol 35 (7) ◽  
pp. 673-676 ◽  
Author(s):  
B. Belleau

The acid catalyzed condensation of cyclohexenylacetic acid and its corresponding N-methylamide with formaldehyde was investigated. Good yields of the expected δ-lactone (V) or δ-lactam (IX) were obtained when trifluoroacetic acid was used both as catalyst and solvent for the reaction.


2016 ◽  
Vol 14 (20) ◽  
pp. 4571-4575 ◽  
Author(s):  
Tao Chen ◽  
Ying-Yeung Yeung

A trifluoroacetic acid catalyzed highly 6-endo regioselective bromocyclization of styrene-type carboxylic acid has been developed.


Synthesis ◽  
2018 ◽  
Vol 51 (06) ◽  
pp. 1377-1382
Author(s):  
Tzenge-Lien Shih ◽  
Min-Chen Tsai ◽  
Pei Huang ◽  
Liang Syu

The reaction of 5-amino-2-[2-(dimethylamino)ethyl]-6-phenyl-1H-benzo[de]isoquinoline-1,3(2H)-dione with a series of aldehydes in acidic media (phosphoric acid, trifluoromethanesulfonic acid, and trifluoroacetic acid) is described. This key step is based on the Pictet–Spengler reaction to synthesize ten novel isoquinolino[5,4-ab]phenanthridine derivatives. The most effective acid is phosphoric acid and optimized yields were obtained. The frameworks of target compounds are unique and have never been reported.


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