dc.creatorRivera, Fausto Ramiro
dc.date2015-06-15T13:58:58Z
dc.date2015-06-15T13:58:58Z
dc.date1978-03
dc.date.accessioned2023-08-11T22:39:59Z
dc.date.available2023-08-11T22:39:59Z
dc.identifier*EC-INIAP-BEESC, Quito (T/R621m)
dc.identifierhttp://repositorio.iniap.gob.ec/handle/41000/1166
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8269764
dc.descriptionThe rate limiting step in the hydration of 1-benzyl-l, 4 — dihydronicotinamide (1a) and 1-benzyl-3-acetyl-l, 4- dihydropyridine (.lb) is; a slow proton transfer, as shown by the kinetic deuterium solvent isotope effects and buffer catalysis. Reactions in dilute HC1 are strongly inhibited by cationic micelles of cetyltrimethylammonium bromide, CTABr, and the inhibition can be related to the micellar binding of the substrates determined spectrophotometrically or by solubility. Anionic micelles of sodium lauryl sulfate, NaLS, only weakly catalyze hydration in dilute HC1, and rate constants go through maxima with increasing [NaLS].
dc.format3 p.
dc.formatapplication/pdf
dc.languageen
dc.publisherSanta Barbara: University of California, 1978. 87 p.
dc.subjectQUÍMICA
dc.subjectMag. Sc. Thesis
dc.titleMicellar effects upon the hydrogen ion and general acid catalyzed hydration of 1,4-Dihydropyridines
dc.typeTesis
dc.coverageE. E. Santa Catalina


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