Publication | Closed Access
Regioselective Synthesis of 7-(Trimethylsilylethynyl)pyrazolo[1,5-<i>a</i>]pyrimidines via Reaction of Pyrazolamines with Enynones
39
Citations
48
References
2016
Year
Product PurificationEngineeringFluorescent PropertiesOrganic ChemistryRegioselective SynthesisEasy AccessChemistryHeterocycle ChemistryStereoselective SynthesisPharmacologySynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
Condensation of enynones readily available from cheap starting material with pyrazolamines provides easy access to fluorescent 7-(trimethylsilylethynyl)pyrazolo[1,5-a]pyrimidines. The reaction is straightforward, does not require the use of any additional reagents or catalysts, and can be performed without inert atmosphere. Various substituents and functional groups in both enynone and pyrazolamine are tolerated. The presented method features full regioselectivity, high isolated yields, and simplicity of both setup and product purification. Fluorescent properties of the obtained pyrazolopyrimidines were studied.
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