نتایج جستجو برای: aminophenol
تعداد نتایج: 862 فیلتر نتایج به سال:
Construction of Escherichia coli strains for conversion of nitroacetophenones to ortho-aminophenols.
The predominant bacterial pathway for nitrobenzene (NB) degradation uses an NB nitroreductase and hydroxylaminobenzene (HAB) mutase to form the ring-fission substrate ortho-aminophenol. We tested the hypothesis that constructed strains might accumulate the aminophenols from nitroacetophenones and other nitroaromatic compounds. We constructed a recombinant plasmid carrying NB nitroreductase (nbz...
Two novel probes were designed, sharing the same BODIPY core but differing only by a minimized variation in the recognition site from 4-hydroxyaniline into 4-methoxyaniline. Such a small change in the reaction site could switch the selective detection from peroxynitrite to HOCl. Undoubtedly, the new designed BODIPY core exhibits valuable properties.
Oor N-arylated aminophenol products constitute a common structural motif in various potentially useful therapeutic agents and/or drug candidates. We have developed a complementary set of Cuand Pd-based catalyst systems for the selective Oand N-arylation of unprotected aminophenols using aryl halides. Selective O-arylation of 3and 4-aminophenols is achieved with copper-catalyzed methods employin...
A molecularly imprinted copolymer, poly(o-phenylenediamine-co-o-aminophenol) (PoPDoAP), was prepared as a new ascorbic acid (AA) sensor. The copolymer was synthesized by incorporation of AA as template molecules during the electrochemical copolymerization of o-phenylenediamine and o-aminophenol, and complementary sites were formed after the copolymer was electrochemically reduced in ammonium aq...
O- or N-arylated aminophenol products constitute a common structural motif in various potentially useful therapeutic agents and/or drug candidates. We have developed a complementary set of Cu- and Pd-based catalyst systems for the selective O- and N-arylation of unprotected aminophenols using aryl halides. Selective O-arylation of 3- and 4-aminophenols is achieved with copper-catalyzed methods ...
An ortho-nitrophenol solution was injected into the intestine which had been removed from an anesthetized mouse by placing a ligature at the duodenum and at the rectum. The intestine was then incubated in Ringer's solution at 37•Ž and the ortho-nitrophenol was found to be reduced to ortho aminophenol. At the same time, it was found that ortho-nitrophenol which was incubated with the intestinal ...
In order to determine phenolic compounds in water, we propose a method based on the reaction of phenolic compounds with 4-aminoantipyrine in the presence of peroxodisulfate at pH 10 to form antipyrine dye and the solid-phase extraction of dye with a Varian Bond Elut Plexa cartridge. Dye collected on the cartridge is eluted with acetonitrile and the absorbance is measured at 475 nm. In our exper...
Oor N-arylated aminophenol products constitute a common structural motif in various potentially useful therapeutic agents and/or drug candidates. We have developed a complementary set of Cuand Pd-based catalyst systems for the selective Oand N-arylation of unprotected aminophenols using aryl halides. Selective O-arylation of 3and 4-aminophenols is achieved with copper-catalyzed methods employin...
Paracetamol that is known as acetaminophen have the most consume as an analgesic and antipyreticdrug in the world. That is formulated in single compound or mixture at many forms such astablets, syrups, suspensions and drops. The last form is intravenous injections. Paracetamol derivedfrom 4-minophenol which is synthesized by acylated the P-acetaminophenol and acetic anhydride.4-aminophenol is t...
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