STRUCTURE OF THE SALTS OF AROMATIC NITRILES

1930 ◽  
Vol 52 (5) ◽  
pp. 1971-1975 ◽  
Author(s):  
Fred W. Upson ◽  
Robert T. Maxwell ◽  
Howard M. Parmelee
Keyword(s):  
1928 ◽  
Vol 50 (6) ◽  
pp. 1699-1707 ◽  
Author(s):  
Mary M. Rising ◽  
Tsoh-Wu Zee

Synlett ◽  
2018 ◽  
Vol 29 (18) ◽  
pp. 2444-2448 ◽  
Author(s):  
Yun-Lai Ren ◽  
Jianji Wang ◽  
Xinzhe Tian ◽  
Fangping Ren ◽  
Xinqiang Cheng ◽  
...  

A direct method was developed for the conversion of benzyl ethers into aryl nitriles by using NH4OAc as the nitrogen source and ­oxygen as the terminal oxidant with catalysis by TEMPO/HNO3; the method is valuable for both the synthesis of aromatic nitriles and for the deprotection of ether-protected hydroxy groups to form nitrile groups in multistep organic syntheses.


2002 ◽  
Vol 2002 (11) ◽  
pp. 560-561 ◽  
Author(s):  
Zhang Guolin ◽  
Hu Yongzhou

1-Amino-3-methylpyridinium mesitylenesulfonate (3) reacts with aromatic nitriles in the presence of potassium hydroxide, undergoing 1,3-dipolar cycloaddition followed by elimination of H2 to give 2-aryl-8-methyl[1,2,4]triazolo[1,5- a]pyridines as the major products, rather than the 6-methyl isomers.


ChemInform ◽  
2010 ◽  
Vol 24 (4) ◽  
pp. no-no
Author(s):  
F. DELGADO ◽  
A. C. CANO ◽  
O. GARCIN ◽  
J. ALVARADO ◽  
L. VELASCO ◽  
...  

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