The invention relates to a method for dealkylating alkyl-substituted aromatic hydrocarbons with the aid of water vapour in the presence of a dealkylation catalyst, by means of a gas containing oxygen.
The dealkylation and hydrogenation may be conducted in a single stage.
The elimination is predominantly hepatic by glucuronidation and N-dealkylation.
Sufentanil is rapidly metabolised to a number of inactive metabolites, with oxidative N- and O-dealkylation being the major routes of elimination.
The other mechanism involves dealkylation of the amino groups.
These are made by dealkylating corresponding 6-alkoxy-9-methyl-10-substituted echibolines, thereby converting the 6-alkoxy group to a 6-hydroxy group, especially using boron tribromide as dealkylating reagent.
Metabolism of anastrozole occurs by N-dealkylation, hydroxylation and glucuronidation.
The elimination is predominantly hepatic by glucuronidation and N-dealkylation.
Metabolism of Anastrozole occurs by N –dealkylation, hydroxylation and glucuronidation.
Rotigotine is metabolised by N-dealkylation as well as direct and secondary conjugation.
The dealkylation-transalkylation system includes dealkylation, non-aromatic product gas separations and transalkylation stages.
Firocoxib is metabolised predominantly by dealkylation and glucuronidation in the liver.
The α-keto bisphosphonate esters can be converted to the corresponding acids by acid hydrolysis or mild silyldealkylation.
Further disclosed is the preparation of 2,3-dihydroxy benzonitrile by dealkylation of 2,3-dialkoxy benzonitrile using suitable aluminum salt-amine complex.
Domperidone undergoes rapid and extensive hepatic metabolism by hydroxylation and N-dealkylation.
Domperidone undergoes rapid and extensive hepatic metabolism by hydroxylation and N-dealkylation.
The present disclosure also provides improved processes for preparing semi-synthetic opioids that incorporate the disclosed methods for N-dealkylation of tertiary amines.
Domperidone undergoes rapid and extensive hepatic metabolism by hydroxylation and N-dealkylation.
68953-80-0 Benzene, mixed with toluene, dealkylation product
N-dealkylation, a major pathway of biotransformation, yields the metabolites monoethylglycinexylidide and glycinexylidide.
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