Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gabriel O, Andrés"'
Autor:
Gabriel O. Andrés, Rita H. de Rossi
Publikováno v:
ARKIVOC, Vol 2003, Iss 10, Pp 127-138 (2003)
Externí odkaz:
https://doaj.org/article/d44101ba47774ba8932087c9c568013e
Publikováno v:
J. Chem. Soc., Perkin Trans. 2. :1502-1505
The kinetics of the hydrolysis of Z-phenyl hydrogen phthalate (Z = H, p-Me, m-Me, m-Cl and p-Cl) was studied in the presence of hydroxypropyl-β-cyclodextrin (HPCD) at pH 2.00, 3.00 and 12.00. In acid solutions these reactions involve two kinetic pro
Publikováno v:
The Journal of Organic Chemistry. 66:7653-7657
The kinetics of the hydrolysis of phthalic anhydride and X-phenyl hydrogen phthalate (X = H, p-Me, m-Cl, and p-Cl) were studied. Several bases accelerate the reaction of phthalic anhydride: acetate, phosphate, N-methyl imidazole, 1,4-diazabicyclo[2,2
Publikováno v:
Photochemistry and photobiology. 83(3)
The enthalpy change, DeltaTH, and volume change, DeltaTV, associated with triplet state formation upon excitation of free-base meso-tetra-(4-sulfonatophenyl)porphyrin, TSPP4-, its Zn derivative, ZnTSPP4-, and meso-tetra-(4-carboxyphenyl)porphyrin, TC
Publikováno v:
The Journal of organic chemistry. 71(20)
The kinetic study of the hydrolysis reaction of Z-substituted phenyl hydrogen maleates (Z = H, m-CH3, p-CH3, m-Cl, p-Cl and m-CN) was carried out in aqueous solution, and the results were complemented with theoretical studies. Under some experimental
Autor:
Rita H. de Rossi, Gabriel O. Andrés
Publikováno v:
The Journal of organic chemistry. 70(4)
[reaction: see text] The kinetic of the reactions of phthalic and maleic anhydrides with different substituted phenols (Z-PhOH with Z = H, m-CH(3), p-CH(3), m-Cl, p-Cl, and m-CN) were studied in aqueous solution. Two kinetic processes well separated
Publikováno v:
Molecules, Vol 5, Iss 3, Pp 405-406 (2000)
Molecules
Volume 5
Issue 3
Pages 405-406
Molecules
Volume 5
Issue 3
Pages 405-406
HPCD inhibits the hydrolysis reaction of monoamides and monoesters of phthalic and maleic acid at pH 2. The magnitude of inhibition depends on the leaving group. For some of the substrates, the reaction in the cavity is more than 100 times slower tha
Publikováno v:
Journal of Physical Chemistry A; Aug2006, Vol. 110 Issue 34, p10185-10190, 6p