Investigation of cationic transformations involving 5-ethynyl-4-arylpyrimidines

An innovative synthetic approach towards 5-ethynyl-4-arylpyrimidines was developed involving acid-catalyzed electrophilic alkylation of phenols with 5-bromopyrimidine, followed by oxidation and palladium-catalyzed Sonogashira cross-coupling reaction. Reactions of these compounds in the presence of t...

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Hlavní autoři:	Shcherbakov, S. V., Щербаков, С. В., Magometov, A. Y., Магометов, А. Ю., Vendin, M. V., Вендин, М. В., Shcherbakova, V. Y., Щербакова, В. Ю., Aksenov, N. A., Аксенов, Н. А., Aksenov, A. V., Аксенов, А. В., Rubin, M. A., Рубин, М. А.
Médium:	Статья
Jazyk:	English
Vydáno:	Elsevier Ltd 2022
Témata:	Acetylenes Cationic rearrangements Heterocyclic chemistry Reaction mechanisms Synthetic methodology
On-line přístup:	https://dspace.ncfu.ru/handle/20.500.12258/19633
Tagy:	Přidat tag Žádné tagy, Buďte první, kdo otaguje tento záznam!

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https://dspace.ncfu.ru/handle/20.500.12258/19633

Investigation of cationic transformations involving 5-ethynyl-4-arylpyrimidines

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