Anticholinesterase activity of monoquaternary ammonium salts containing hydrophobic radicals

1988 ◽  
Vol 22 (6) ◽  
pp. 452-456
Author(s):  
I. I. Bityukova ◽  
N. D. Igumnova ◽  
N. V. Klimova ◽  
V. M. Solov'ev ◽  
A. P. Skoldinov ◽  
...  
ChemInform ◽  
1988 ◽  
Vol 19 (49) ◽  
Author(s):  
I. I. BITYUKOVA ◽  
N. D. IGUMNOVA ◽  
N. V. KLIMOVA ◽  
V. M. SOLOV'EV ◽  
A. P. SKOLDINOV ◽  
...  

2020 ◽  
Vol 206 ◽  
pp. 112584 ◽  
Author(s):  
Ondrej Soukup ◽  
Marketa Benkova ◽  
Rafael Dolezal ◽  
Radek Sleha ◽  
David Malinak ◽  
...  

1981 ◽  
Vol 15 (9) ◽  
pp. 687-688
Author(s):  
N. S. Volkova ◽  
T. B. Primakova ◽  
S. D. Sokolov

2021 ◽  
Vol 03 (04) ◽  
pp. e194-e199
Author(s):  
Liang Chen ◽  
Wei-Yuan Liu ◽  
Si-Ju Bi ◽  
Ting Zhou ◽  
Jing Pan ◽  
...  

A series of mono- or bis-quaternary ammonium salts derived from cinchonidine or quinine was synthesized and screened as potent phase-transfer catalysts for the reaction of aza-Michael cyclization, the key step in the synthesis of letermovir. During the reaction of aza-Michael cyclization, the screened monoquaternary ammonium salt quinine derivative Q1 transferred 7 to 8 with 91.9% yield and 58% ee. The application of Q1 was preferred, due to its enantioselectivity, the possibility of reuse, and the lower cost in large-scale preparation. Furthermore, the racemization condition of letermovir enantiomer was also explored for the possibility to develop the resolution/racemization process. With the optimal catalyst Q1 in hand, the synthesis of letermovir may be more convenient and economical in the future.


2019 ◽  
Author(s):  
Nikolaus Gorgas ◽  
Berthold Stöger ◽  
Luis F. Veiros ◽  
Karl Kirchner

We report on the first synthesis and structural characterization of the iron based aminoborane complexes. These species are formed upon protonation of a borohydride complex by ammonium salts.<br>


2019 ◽  
Vol 484 (1) ◽  
pp. 104-108
Author(s):  
G. F. Makhaeva ◽  
E. F. Shevtsova ◽  
N. P. Boltneva ◽  
N. V. Kovaleva ◽  
E. V. Rudakova ◽  
...  

This study presents the synthesis of binary tetrohydro-γ-carbolines with ditriazol spacers of varying length, which exhibit anticholinesterase and antioxidant activity, as compared to the original Dimebon prototype. Anticholinesterase activity suggests the potential ability of the new compounds to block β-amyloid aggregation induced by anticholinesterase, making them promising candidates for further research preparations for the treatment of Alzheimer's disease. Particular attention should be paid to the conjugate with an intertriazol hexamethylene spacer, which can be regarded as the leading compound in this series.


2010 ◽  
Vol 7 (1) ◽  
pp. 1-4 ◽  
Author(s):  
Jiri Binder ◽  
Martin Paar ◽  
Daniel Jun ◽  
Miroslav Pohanka ◽  
Martina Hrabinova ◽  
...  

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