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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.


Papers
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Journal ArticleDOI
TL;DR: Three unstable products can be partially isolated from acid hydrolyzates of glutaraldehyde-treated proteins or from the reaction mixtures of glutARaldehyde and model compounds; two of these products have strong ultraviolet absorption near 265 nm.

218 citations

Journal ArticleDOI
TL;DR: The enantioselective addition reaction of terminal acetylenes and aldehydes mediated by Zn(OTf)2 and N-methyl ephedrine can be conducted with reagent grade solvent containing 84-1000 ppm H2O.

218 citations

Patent
10 Jan 2000
TL;DR: In this paper, a method and reagent composition for covalent attachment of target molecules, such as nucleic acids, onto the surface of a substrate is presented, which can be used to provide activated slides for use in preparing microarrays of nucleic acid.
Abstract: Method and reagent composition for covalent attachment of target molecules, such as nucleic acids, onto the surface of a substrate. The reagent composition includes groups capable of covalently binding to the target molecule. Optionally, the composition can contain photoreactive groups for use in attaching the reagent composition to the surface. The reagent composition can be used to provide activated slides for use in preparing microarrays of nucleic acids.

218 citations

Journal ArticleDOI
TL;DR: An artificial system that co-encapsulates multiple catalysts and substrates within the confined space defined by an M12L24 nanosphere that contains 24 endohedral guanidinium-binding sites is reported, demonstrated to strongly bind sulfonate-containing gold catalysts.
Abstract: Tuning reagent and catalyst concentrations is crucial in the development of efficient catalytic transformations. In enzyme-catalysed reactions the substrate is bound-often by multiple non-covalent interactions-in a well-defined pocket close to the active site of the enzyme; this pre-organization facilitates highly efficient transformations. Here we report an artificial system that co-encapsulates multiple catalysts and substrates within the confined space defined by an M12L24 nanosphere that contains 24 endohedral guanidinium-binding sites. Cooperative binding means that sulfonate guests are bound much more strongly than carboxylates. This difference has been used to fix gold-based catalysts firmly, with the remaining binding sites left to pre-organize substrates. This strategy was applied to a Au(I)-catalysed cyclization of acetylenic acid to enol lactone in which the pre-organization resulted in much higher reaction rates. We also found that the encapsulated sulfonate-containing Au(I) catalysts did not convert neutral (acid) substrates, and so could have potential in the development of substrate-selective catalysis and base-triggered on/off switching of catalysis.

217 citations

Journal ArticleDOI
Fei Wang1, Dinghai Wang1, Xin Mu1, Pinhong Chen1, Guosheng Liu1 
TL;DR: A novel copper-catalyzed intermolecular trifluoromethylarylation of alkenes is developed using less active ether-type Togni's reagent under mild reaction conditions and preliminary mechanistic studies reveal that a mutual activation process between arylboronic acid and CF3(+) reagent is essential.
Abstract: A novel copper-catalyzed intermolecular trifluoromethylarylation of alkenes is developed using less active ether-type Togni’s reagent under mild reaction conditions. Various alkenes and diverse arylboronic acids are compatible with these conditions. Preliminary mechanistic studies reveal that a mutual activation process between arylboronic acid and CF3+ reagent is essential. In addition, the reaction might involve a rate-determining transmetalation, and the final aryl C–C bond is derived from reductive elimination of the aryl(alkyl)Cu(III) intermediate.

217 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20232,117
20224,093
2021785
20201,317
20191,860
20182,158