Electronic Substituent Effects on the Acid-Catalyzed [4+ + 2] Cycloaddition of Isopyrazoles with Cyclopentadiene and the Photochemical and Thermal Denitrogenation of the Resulting 1,4-Diaryl-7,7-dimethyl-2,3-diazabicyclo[2.2.1]hept-2-ene Azoalkanes to Bicyclo[2.1.0]pentanes

1994 ◽  
Vol 59 (14) ◽  
pp. 3786-3797 ◽  
Author(s):  
Waldemar Adam ◽  
Heinrich M. Harrer ◽  
Werner M. Nau ◽  
Karl Peters
1986 ◽  
Vol 51 (3) ◽  
pp. 564-572 ◽  
Author(s):  
Oldřich Pytela ◽  
Stanislava Štumrová ◽  
Miroslav Ludwig ◽  
Miroslav Večeřa

Ten 3-hydroxy-1-(X-phenyl)-3-phenyltriazines have been synthesized, and kinetics of their solvolysis have been measured in 40% (v/v) ethanol and sulphuric acid. The concept of kinetic acidity function has been generalized, its construction has been suggested, and the procedure has been applied to the solvolysis of 3-hydroxy-1,3-diphenyltriazenes. The kinetic acidity function found has been confronted with the H0 acidity function. The substituent effects have been evaluated with respect to mechanism of the acid catalyzed solvolysis.


1977 ◽  
Vol 8 (32) ◽  
pp. no-no
Author(s):  
S. Y. ATTIA ◽  
J. P. BERRY ◽  
K. M. KOSHY ◽  
Y.-K. LEUNG ◽  
E. P. JUN. LYZNICKI ◽  
...  

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