P.B. Venuto

TL;DR: A number of crystalline aluminosilicates have been shown to be versatile catalysts for the alkylation of simple monocyclic aromatic nuclei such as benzene, phenol, and thiophene, with a wide variety of alkylating agents as mentioned in this paper.

TL;DR: In this paper, sites active for alkylation in these three acidic faujasites are visualized as strongly acidic and ultimately protonic, and complex intracyrstalline polymerization-hydrogen transfer reactions of the olefin were shown to be responsible for catalyst aging.

TL;DR: In this paper, a hydrogen Y zeolite was used for the rearrangement of ketoximes to amides, and 75% to 95% yields of amides were obtained.

TL;DR: In this paper, conditions for efficient condensation of carbonyl compounds and aromatics with minimum catalyst aging were provided. And the observed product distributions generally suggest the operation of carbonium-ion-type mechanisms.

TL;DR: In this article, a role for polar or ionic intermediates was suggested for these dehydrohalogenation reactions, and it was shown that rare-earth-exchanged X zeolite was inhibited by nitrogenous bases.