Hydration of 3-methyl-3-norcarene epoxides under acid and basic catalysis conditions

Author(s):  
�. Kh. Kazakova ◽  
L. N. Surkova ◽  
S. V. Andreeva
Keyword(s):  

2021 ◽  
Vol 45 (8) ◽  
pp. 3833-3847 ◽  
Author(s):  
Alexandra Rodrigues ◽  
Bruno Sena da Fonseca ◽  
Ana Paula Ferreira Pinto ◽  
Susana Piçarra ◽  
M. Fátima Montemor

TEOS-based sols following basic catalysis routes were explored and showed high potential and important advantages for consolidation of soft limestone.



2019 ◽  
Vol 282 ◽  
pp. 159-168 ◽  
Author(s):  
Karina Arruda Almeida ◽  
Peter Hammer ◽  
Dilson Cardoso
Keyword(s):  


2019 ◽  
Vol 9 (21) ◽  
pp. 6007-6014 ◽  
Author(s):  
Javier Luis-Barrerra ◽  
Rafael Cano ◽  
Ghazaleh Imani-Shakibaei ◽  
Javier Heras-Domingo ◽  
Javier Pérez-Carvajal ◽  
...  

Non-covalent inclusion of small acid and base molecules in an imine structure based on COF-300 nanoparticles is presented.





2008 ◽  
Vol 46 (18) ◽  
pp. 1891-1902 ◽  
Author(s):  
Benoît Didier ◽  
Régis Mercier ◽  
Nicole D. Alberola ◽  
Corine Bas


1928 ◽  
Vol 50 (8) ◽  
pp. 2305-2311 ◽  
Author(s):  
James B. Conant ◽  
George M. Bramann


2020 ◽  
Vol 205 ◽  
pp. 106427 ◽  
Author(s):  
Angela Sanchez-Sanchez ◽  
Maria Teresa Izquierdo ◽  
Sandrine Mathieu ◽  
Ghouti Medjahdi ◽  
Vanessa Fierro ◽  
...  


Kinetic measurements have been made at 25° on the catalysed halogenation of the following ketones: acetone, acetonylacetone, monochloroacetone, monobromoacetone, as . dichloroacetone and acetylacetone. In all cases the reactions are of zero order with respect to the halogen and exhibit general basic catalysis. For the first two ketones general acid catalysis is also detectable. For each ketone the catalytic constants k B of four carboxylate anions are related to the dissociation constants K A of the corresponding acids by an equation of the type k B = G (1/ K A ) α , where G and the α are constants for a given ketone. The catalytic constants measured cover a range of about 10 8 . Examination of the results (together with those of Pedersen for the bromination of acetoacetic ester and acetoacetic acid) shows that the exponent α decreases steadily from 0.88 to 0.48 as the reactivity of the ketone increases. The catalytic coefficients of the water molecule are given approximately by the equations valid for the carboxylate anions, but the hydroxyl ion is in each case much less effective as a catalyst than these equations predict.



1954 ◽  
pp. 241-270
Author(s):  
Martin Kilpatrick


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