scholarly journals Synthesis and Structure−Activity Relationships of Conformationally Constrained Histamine H3Receptor Agonists

2003 ◽  
Vol 46 (25) ◽  
pp. 5445-5457 ◽  
Author(s):  
Ruengwit Kitbunnadaj ◽  
Obbe P. Zuiderveld ◽  
Iwan J. P. De Esch ◽  
Roeland C. Vollinga ◽  
Remko Bakker ◽  
...  
1994 ◽  
Vol 59 (3) ◽  
pp. 675-682 ◽  
Author(s):  
Fridrich Gregáň ◽  
Viktor Kettmann ◽  
Pavol Novomeský ◽  
Július Sivý

The synthesis of two pairs of the title diastereomers, which represent conformationally constrained analogues of the phenylcarbamate local anesthetics, is described. The synthesis was accomplished by starting from cycloheptanone and 2-alkoxyanilines and the intermediate diastereomers of 2-aminomethylcycloalkanols (VI, VII) were separated as their 4-nitrobenzoyl derivatives (IV, V) by extraction and fractional crystallization. The prepared compounds (VIIIa, VIIIb, IXa, and IXb) are assumed to be of help in interpreting the structure activity relationships within this class of drugs.


Planta Medica ◽  
2008 ◽  
Vol 74 (09) ◽  
Author(s):  
Q Do ◽  
H Doan Thi Mai ◽  
T Gaslonde ◽  
B Pfeiffer ◽  
S Léonce ◽  
...  

Planta Medica ◽  
2012 ◽  
Vol 78 (11) ◽  
Author(s):  
M Reis ◽  
RJ Ferreira ◽  
MMM Santos ◽  
DJVA dos Santos ◽  
J Molnár ◽  
...  

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