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- W3136368162 abstract "An efficient method for the synthesis of pharmaceutically prospective pyrrole–aminopyrimidine ensembles (in up to 91% yield) by the cyclocondensation of easily available acylethynylpyrroles with guanidine nitrate has been developed. The reaction proceeds under heating (110–115 °C, 4 h) in the KOH/DMSO system. In the case of 2-benzoylethynylpyrrole, the unexpected addition of the formed pyrrole–aminopyrimidine as N- (NH moiety of the pyrrole ring) and C- (CH of aminopyrimidine) nucleophiles to the triple bond is observed." @default.
- W3136368162 created "2021-03-29" @default.
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- W3136368162 date "2021-03-17" @default.
- W3136368162 modified "2023-10-16" @default.
- W3136368162 title "Pyrrole–Aminopyrimidine Ensembles: Cycloaddition of Guanidine to Acylethynylpyrroles" @default.
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- W3136368162 doi "https://doi.org/10.3390/molecules26061692" @default.
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