Reagent

About: Reagent is a research topic. Over the lifetime, 60091 publications have been published within this topic receiving 1234928 citations. The topic is also known as: reagens.

Glucose detection system free from fluoride-ion interference

Abstract: An improved multilayer element for detecting glucose in samples of biological fluid which may contain with fluoride ion as a contaminant or preservative is described. The improved element comprises a buffered Trinder's reagent, which reagent comprises glucose oxidase, peroxidase, 4-aminoantipyrine and a phenolic or naphtholic coupler, which is buffered to a pH between about 4.5 and about 6.0. Such a buffering reduces any interference which may be due to fluoride ion present in the sample under analysis.

2'-Nitro-2'-propen-1'-yl 2,2-dimethylpropanoate (NPP), a multiple coupling reagent

Abstract: The title compound 1 (NPP) is prepared from formaldehyde, nitromethane, an pivaloyl chloride. It is shown to be a versatile nitroallylating reagent combining with nucleophiles as different as anilines, indoles, enolates, and organolithium compounds. This is documented by ca. 40 examples (2–30). The mechanism of the reaction is discussed. Some examples of addition of two different nucleophiles to the C3-moiety of NPP are described (35-46). This demonstrates the usefulness of NPP as a multiple coupling reagent for convergent syntheses, also of products not containing nitro groups ((Scheme 4)).

Rhodium-catalyzed, regiospecific functionalization of polyolefins in the melt.

Abstract: The rhodium-catalyzed, terminal-selective borylation of alkanes has been used to modify polyolefins. The functionalization of two materials, polyethylethylene (PEE) of molecular weights 1200 and 37 000, was conducted by combining bis-pinacoldiboron and 2.5 mol % [Cp*RhCl2]2 in neat polymer and heating at 150 °C. This procedure causes the polymer and boron reagent to melt, the catalyst to dissolve, and the reaction to form material with boryl groups at the terminal position of the polymer side chains. Oxidation of the borylated material generated polymers with hydroxyl groups at the terminal position of the side chains. The functionalization was conducted at various ratios of boron reagent to monomer. The resulting borylated and subsequent hydoxylated materials were characterized by 1H and 13C NMR spectroscopy, as well as MALDI-MS and GPC. Little change in polymer molecular weight and polydispersity was observed, and these data indicate that scission of the main chain does not occur. Measurements of the Tg...