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1.
Org Biomol Chem ; 15(18): 3924-3929, 2017 May 10.
Artículo en Inglés | MEDLINE | ID: mdl-28430269

RESUMEN

An easily available Pd(OAc)2/(2-(anthracen-9-yl)-1H-inden-3-yl) dicyclohexylphosphine/toluene/iPrOH/water catalytic system was developed, which shows high catalytic activity in the Suzuki-Miyaura cross-coupling reactions of a diverse array of aryl and heteroaryl chlorides with Pd loadings down to 0.01 mol%.

2.
Org Biomol Chem ; 15(27): 5805-5810, 2017 Jul 21.
Artículo en Inglés | MEDLINE | ID: mdl-28660941

RESUMEN

An efficient solvent-free protocol for the Buchwald-Hartwig cross-coupling reaction of aryl and heteroaryl chlorides with primary and secondary amines using the Pd(dba)2/ligand 1 catalytic system has been developed. Notably, the catalytic system also efficiently catalyzed the reaction under aqueous conditions.

3.
Chem Commun (Camb) ; 57(82): 10711-10714, 2021 Oct 14.
Artículo en Inglés | MEDLINE | ID: mdl-34553711

RESUMEN

Herein, we describe a soluble iron(II)-phthalocyanine, [FeII(tBu4Pc)(py)2] (Pc = phthalocyaninato(2-)), as an effective catalyst in intramolecular C(sp3)-H bond amination, with alkyl azides as the nitrogen source, to afford the amination products in moderate to excellent yields with a broad substrate scope.

4.
Anal Sci ; 34(8): 959-964, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-30101892

RESUMEN

DNA methyltransferase (MTase) is related to transcriptional repressor activity in biological functions. It is an essential for cancer diagnosis and therapeutics to detect DNA MTase activity sensitively. Here, a fluorescent system based on polymerase amplification has been developed to detect DNA adenine MTase (Dam) activity sensitively. The amplification is triggered by the probe DNA regions a, which are the primes of a polymerase-induced replicated reaction. They come from methylation and a digestion reaction of DNA S1-S1, including a 5'-GATC-3' sequence recognized by Dam MTase and methylation sensitive restriction endonuclease Dpn I. The intensities of fluorescence are dependent on the Dam MTase activity. The method shows fine sensitivity with a detection limit of 3.2 × 10-4 U mL-1 and specificity for Dam MTase. In human serum samples, the method has been successfully applied, and it has also been used to screen the inhibitors, which means that the developed method can be a powerful and potential tool for drug development and clinical diagnosis in the future.


Asunto(s)
Técnicas Biosensibles , Pruebas de Enzimas/métodos , Fluorescencia , Técnicas de Amplificación de Ácido Nucleico/métodos , Metiltransferasa de ADN de Sitio Específico (Adenina Especifica)/análisis , Metiltransferasa de ADN de Sitio Específico (Adenina Especifica)/metabolismo , Sondas de ADN/química , Sondas de ADN/metabolismo , Humanos , Espectrometría de Fluorescencia
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