N-substituted carbamic acid esters: Synthesis, anticholinesterase activity, and calcium ion antagonism

1995 ◽  
Vol 29 (11) ◽  
pp. 757-759
Author(s):  
Yu. Ya. Ivanov ◽  
N. M. Smirnova
1982 ◽  
Vol 13 (51) ◽  
Author(s):  
GORODETSKYL. SH. GORODETSKYL. SH. ◽  
O. N. VOLZHINA ◽  
I. A. KUZNETSOVA ◽  
E. N. ALEKSEEVA
Keyword(s):  

1973 ◽  
Vol 28 (5-6) ◽  
pp. 339-352 ◽  
Author(s):  
Hartmut Schultze

The photolysis of N-aryl-carbamic acid alkyl esters in methanol was investigated. The primary products, amino-benzoic acid esters and aromatic amines, result from photo-Fries rearrangements and splitting processes.2,4,6-Trimethylphenyl-carbamic acid ethyl ester and N-alkyl-carbamic acid alkyl esters form photolysis products only through homolytic splitting reactions.The photooxidation of N-substituted urethanes has been investigated in tert.-butanol. The main products are primary amines and CO2.These initially formed compounds are then further oxidized. In the aliphatic substituted derivatives, oxidation of the N-alkyl group results followed homolytic bond splitting.


1992 ◽  
Vol 81 (4) ◽  
pp. 380-385
Author(s):  
Gregory M. Shutske ◽  
John D. Tomer ◽  
Kevin J. Kapples ◽  
Nicholas J. Hrib ◽  
John G. Jurcak ◽  
...  

ChemInform ◽  
2011 ◽  
Vol 42 (52) ◽  
pp. no-no
Author(s):  
Antonio Garofalo ◽  
Laurence Goossens ◽  
Perrine Six ◽  
Nicolas Lebegue ◽  
Patrick Depreux

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