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ChemInform Abstract: Hydrolysis of Cyclodisilazanes.
ChemInform, 1989AbstractThe relatively unhindered cyclodisilazane (I) readily undergoes hydrolysis in the presence of catalytic amounts of acid or base.
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Hydrolysis of esters by staphylococci
International Journal of Food Microbiology, 1997The objective of this work was to characterize the hydrolysis of esters by staphylococci in order to understand if they could contribute to the release of free fatty acids in sausage. Cell-free extracts and extracellular concentrates of staphylococci were examined for esterase activities against p-nitrophenyl esters and for lipolytic activities against
Talon, Régine, Montel, Marie-Christine
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Hydrolysis and protection from hydrolysis of enkephalins in human plasma
Neurochemical Research, 1990Seven groups of enkephalin-degrading enzymes and three groups of inhibitors active on these enzymes were separated from human plasma. The activity of the enzymes in hydrolyzing enkephalins and of the inhibitors in protecting enkephalins from proteolysis was measured.
Gianna Roscetti +4 more
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2016
The glycosidic bond might be degraded by chemical and/or enzymatic agents. Comparative studies revealed that chemical hydrolysis is nonspecific and on the other hand the enzymatic is regiospecific and stereospecific. The glycosides are chemically susceptible to acid conditions and only in some cases to basic conditions.
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The glycosidic bond might be degraded by chemical and/or enzymatic agents. Comparative studies revealed that chemical hydrolysis is nonspecific and on the other hand the enzymatic is regiospecific and stereospecific. The glycosides are chemically susceptible to acid conditions and only in some cases to basic conditions.
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Bulletin of Environmental Contamination and Toxicology, 2006
L. Guoguang +4 more
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L. Guoguang +4 more
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1996
Abstract There are two general approaches to the use of hydrolysis and esterification in asymmetric synthesis, and usually both involve the use of enzymes as asymmetric catalysts. In one case the asymmetric catalyst is used in a kinetic resolution process in which one enantiomer of a racemic mixture reacts more rapidly than its antipode.
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Abstract There are two general approaches to the use of hydrolysis and esterification in asymmetric synthesis, and usually both involve the use of enzymes as asymmetric catalysts. In one case the asymmetric catalyst is used in a kinetic resolution process in which one enantiomer of a racemic mixture reacts more rapidly than its antipode.
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