Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/22300
Title: Annulation of Perimidines with 5-Alkynylpyrimidines en Route to 7-Formyl-1,3-Diazopyrenes
Authors: Shcherbakov, S. V.
Щербаков, С. В.
Aksenov, A. V.
Аксенов, А. В.
Vendin, M. V.
Вендин, М. В.
Shcherbakova, V. Y.
Щербакова, В. Ю.
Ivanova, A. Y.
Иванова, А. Ю.
Shcheglov, M. O.
Щеглов, М. О.
Ovcharov, S. N.
Овчаров, С. Н.
Rubin, M. A.
Рубин, М. А.
Keywords: Brønsted acid catalysis;Acetylenes;Annulations;Nitrogen heterocycles;Rearrangements
Issue Date: 2022
Citation: Shcherbakov, S.V., Aksenov, A.V., Vendin, M.V., Shcherbakova, V.Y., Ivanova, A.Y., Shcheglov, M.O., Ovcharov, S.N., Rubin, M. Annulation of Perimidines with 5-Alkynylpyrimidines en Route to 7-Formyl-1,3-Diazopyrenes // International journal of molecular sciences. - 2022. - 23 (24), статья № 15657. - DOI: 10.3390/ijms232415657
Series/Report no.: International Journal of Molecular Sciences
Abstract: Unusual rearrangements were shown to accompany Brønsted acid-assisted peri-annulations of 1H-perimidines with 5-alkynylpyrimidines. These transformations take different routes depending on the nature of acetylene precursor, and lead to the formation of 7-formyl-1,3-diazopyrenes.
URI: http://hdl.handle.net/20.500.12258/22300
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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