E. Yu. Schmidt, I. V. Tatarinova, E. V. Ivanova, B. A. Trofimov, “2-Aminopyrimidines in just two steps from ketones, acetylenes and guanidine via β,γ enones”, Mendeleev Commun., 27:3 (2017), 283

Эта публикация цитируется в 6 статьях

Communications

2-Aminopyrimidines in just two steps from ketones, acetylenes and guanidine via β,γ enones

E. Yu. Schmidt, I. V. Tatarinova, E. V. Ivanova, B. A. Trofimov

A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation

Аннотация: Available β,γ-enones, the products of nucleophilic addition of ketones to phenylacetylene, react with guanidine in the KOH / DMSO system at 70°C to give 2-aminopyrimidines in up to 72% yield.

Язык публикации: английский

DOI: 10.1016/j.mencom.2017.05.022

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