Results 211 to 220 of about 451,494 (235)
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Journal of Pharmaceutical Sciences, 1964
Data are presented for the hydrolytic degradation of idoxuridine (5-iodo-2′-deoxyuridine) in aqueous solution over a wide range of hydrogen ion concentration (pH 1.3 to 12.0). The over-all reaction rate was experimentally equal to k 1 [ H + ] [ H + ] + K a + k 2 K a K a + [ H + ] + k 3 K ...
L J, RAVIN +3 more
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Data are presented for the hydrolytic degradation of idoxuridine (5-iodo-2′-deoxyuridine) in aqueous solution over a wide range of hydrogen ion concentration (pH 1.3 to 12.0). The over-all reaction rate was experimentally equal to k 1 [ H + ] [ H + ] + K a + k 2 K a K a + [ H + ] + k 3 K ...
L J, RAVIN +3 more
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Hydrolysis of cyclodisilazanes
Organometallics, 1989Abstract Unhindered N,N′-diphenyltetramethylcyclodisilazane readily undergoes hydrolysis in the presence of catalytic amounts of acid or base. Under base conditions an intermediate diaminodisiloxane may be isolated. The more sterically congested hexaphenylcyclodisilazane is resistant to acid hydrolysis but is readily hydrolyzed in the presence of base.
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1965
Publisher Summary The chapter illustrates that the studies of hydrolytic agents have led to major advances in our knowledge of proteins, including the identification of the amino acid constituents of proteins and the development of the polypeptide concept of protein structure.
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Publisher Summary The chapter illustrates that the studies of hydrolytic agents have led to major advances in our knowledge of proteins, including the identification of the amino acid constituents of proteins and the development of the polypeptide concept of protein structure.
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7.6 Hydrolysis and Reverse Hydrolysis: Hydrolysis and Formation of Amides
2012V. Gotor, V. Gotor-Fernández, E. Busto
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