Semisynthesis and pharmacological investigation of lipo-alkaloids prepared from aconitine by transesterification with eicosanoic acid analogues

Planta Medica ◽  
2010 ◽  
Vol 76 (12) ◽  
Author(s):  
B Borcsa ◽  
U Widowitz ◽  
D Csupor ◽  
P Forgo ◽  
R Bauer ◽  
...  
2017 ◽  
Author(s):  
B Tóth ◽  
N Kúsz ◽  
N Bózsity ◽  
I Zupkó ◽  
V Csizmadia ◽  
...  

Author(s):  
Hussein I. El-Subbagh

Abstract:: Thiazolo- and thiadiazolo-[3,2-a][1,3]diazepines and their patented derivatives, tested with diverse CNS pharmacological activities, constitute an important class of compounds for new drug development. Therefore, research efforts were continued to design, synthesize, and evaluate compounds for their ultra-short, short-acting hypnotic, anticonvulsant, and neuromuscular blocking activities. The present review provides a summary of the work accomplished by these heterocycles and their biological evaluation.


1976 ◽  
Vol 10 (10) ◽  
pp. 1318-1320
Author(s):  
V. A. Golovkin ◽  
E. P. Lukash ◽  
V. R. Stets ◽  
B. V. Kurmaz

ChemInform ◽  
2010 ◽  
Vol 24 (1) ◽  
pp. no-no
Author(s):  
M. DE AMICI ◽  
C. DALLANOCE ◽  
C. DE MICHELI ◽  
E. GRANA ◽  
A. BARBIERI ◽  
...  

Peptides ◽  
2019 ◽  
Vol 112 ◽  
pp. 106-113 ◽  
Author(s):  
Anna I. Erdei ◽  
Adina Borbély ◽  
Anna Magyar ◽  
Edina Szűcs ◽  
Ferenc Ötvös ◽  
...  

1950 ◽  
Vol 28b (9) ◽  
pp. 556-560 ◽  
Author(s):  
F. A. Vandenheuvel ◽  
P. Yates

The Arndt–Eistert reaction offers a convenient method for the synthesis of the higher members of the aliphatic carboxylic acid series. Nonadecanoic acid, eicosanoic acid, and heneicosanoic acid have been prepared successively from stearic acid in good yields. An efficient method of purification of the synthetic products is described. The ultraviolet absorption maxima for some diazoketones derived from the higher members of the aliphatic carboxylic acid series are recorded.


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