Acetylene derivatives of 1,2,4-triazole

Author(s):  
S. F. Vasilevskii ◽  
A. N. Sinyakov ◽  
M. S. Shvartsberg ◽  
I. L. Kotlyarevskii
1985 ◽  
Vol 107 (12) ◽  
pp. 3717-3718 ◽  
Author(s):  
Helmut G. Alt ◽  
Heidi E. Engelhardt ◽  
Marvin D. Rausch ◽  
Lawrence B. Kool

2000 ◽  
Vol 49 (4) ◽  
pp. 631-641 ◽  
Author(s):  
L. S. Khaikin ◽  
O. E. Grikina ◽  
V. A. Sipachev ◽  
A. V. Belyakov ◽  
E. T. Bogoradovskii

1980 ◽  
Vol 66 ◽  
pp. 149-158 ◽  
Author(s):  
L.S. Khaikin ◽  
A.V. Belyakov ◽  
L.V. Vilkov ◽  
E.T. Bogoradovskii ◽  
V.S. Zavgorodnii

Author(s):  
M. S. Shvartsberg ◽  
S. F. Vasilevskii ◽  
R. Z. Sagdeev ◽  
I. L. Kotlyarevskii

ChemInform ◽  
2010 ◽  
Vol 26 (19) ◽  
pp. no-no
Author(s):  
K. KOMATSU ◽  
Y. MURATA ◽  
N. TAKIMOTO ◽  
S. MORI ◽  
N. SUGITA ◽  
...  

1972 ◽  
Vol 5 (6) ◽  
pp. 797-800 ◽  
Author(s):  
M. S. Shvartsberg ◽  
S. F. Vasilevskii ◽  
V. G. Kostrovskii ◽  
I. L. Kotlyarevskii

2021 ◽  
Author(s):  
Andrey I Puzanov ◽  
Dmitry S Ryabukhin ◽  
Anna S Zalivatskaya ◽  
Dmitriy N Zakusilo ◽  
Darya S Mikson ◽  
...  

Acetylene derivatives of 1,2,4-oxadiazoles, 5-(2-arylethynyl)-3-aryl-1,2,4-oxadiazoles, have been obtained, for the first time, from 5-(2-arylethenyl)-3-aryl-1,2,4-oxadiazoles by their bromination at the carbon-carbon double bond followed by di-dehydrobromination with NaNH2 in liquid NH3.  Reaction of the acetylene 1,2,4-oxadiazoles with arenes in neat triflic acid TfOH (CF3SO3H) at room temperature for 1 h result in the formation of E-/Z-5-(2,2-diarylethenyl)-3-aryl-1,2,4-oxadiazoles as products of regioselective hydroarylation of the acetylene bond. Addition of TfOH to acetylene bond of these oxadiazoles gives rise quantitatively to E-/Z-vinyl triflates. Reaction cationic intermediates have been studied by DFT calculations. The reaction mechanisms have been discussed.


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