Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Pedro S. M. Oliveira"'
Autor:
Luciano M. Lião, Lorrane Santos Vilela, Pedro S. M. Oliveira, Francisco Fernandes Gambarra Neto, Carlos Frederico de Souza Castro, Eduardo Vieira Silveira
Publikováno v:
Industrial Crops and Products. 97:545-551
This paper describes the physicochemical and chromatographic characterization of crambe oil and the process of its methyl transesterification via alkaline catalysis using response surface methodology (RSM). The reaction conditions developed by applyi
Autor:
José R. Mora, Anthony J. Kirby, Nicholas H. Williams, Pedro S. M. Oliveira, Michelle Medeiros, Faruk Nome, Almahdi Amer
Publikováno v:
The Journal of Organic Chemistry. 78:1343-1353
Notwithstanding its half-life of 70 years at 25 °C, the spontaneous hydrolysis of the anion of di-2-pyridyl phosphate (DPP) is thousands of times faster (ca. 3000 at 100 °C, over 10000-fold at 25 °C) than expected for a diester with leaving groups
Autor:
Faruk Nome, Boniek G. Vaz, Pedro S. M. Oliveira, Anthony J. Kirby, Eduardo H. Wanderlind, Michelle Medeiros, Elisa S. Orth, Marcos N. Eberlin
Publikováno v:
The Journal of organic chemistry. 76(19)
The phosphorylation of imidazole by two activated phosphate diesters and a triester gives phosphorylimidazole derivatives that are stable enough in aqueous solution to be observed and identified by ESI-MS/MS and NMR. Half-lives ranging from hours to
Autor:
Anthony J. Kirby, Eduardo H. Wanderlind, Faruk Nome, Michelle Medeiros, Elisa S. Orth, Pedro S. M. Oliveira, Tiago A. S. Brandão, Nicholas H. Williams, Almahdi Amer
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 17(52)
The high rate of spontaneous hydrolysis of tris-2-pyridyl phosphate (TPP) is explained by the activating effects of the non-leaving ("spectator") groups on P-OAr cleavage, and not by intramolecular catalysis. Previous work on phosphate-transfer react
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 15(34)
We have identified the first highly efficient intramolecular general base catalysis (IGBC) of a hydrolysis reaction, in a system where two general bases are available to assist the attack of the same nucleophilic water molecule. The suggested mechani