125488-15-5Relevant academic research and scientific papers
DUPLEX STABILIZING FLUORESCENCE QUENCHERS FOR NUCLEIC ACID PROBES
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Paragraph 0215-0216, (2019/03/05)
Diaryl-azo derivatives are efficient fluorescence quenchers as well as nucleic acid duplex-stabilizing agents and are useful in oligonucleotide conjugates and probes. The oligonucleotide-quencher conjugates may be used in detection methods for nucleic acid targets.
A simple, three-component synthesis of 2-aminothiazoles using trimethylsilyl isothiocyanate
Golubev, Viktor,Zubkov, Fedor,Krasavin, Mikhail
, p. 4844 - 4847 (2013/08/28)
The first multicomponent, solution-phase protocol to prepare privileged 2-aminothiazoles from α-bromocarbonyl compounds and amines (aromatic and aliphatic) using commercially available trimethylsilyl isothiocyanate is described.
Substituted 2-Aminothiazoles from α-Thiocyanato-acetophenones and Dialkylamines
Teller, J.,Dehne, H.,Zimmermann, T.,Fischer, G. W.,Olk, B.
, p. 453 - 460 (2007/10/02)
α-Thiocyanato-acetophenones 1 react with dialkylammonium salts of weak acids (acetates, propionates, benzoates) to give 2-dialkylamino-4-aryl-thiazoles 4.As reaction medium aliphatic alcohols (methanol, ethanol), dipolar-aprotic solvents (acetonitrile, di
