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Annulation of Perimidines with 5-Alkynylpyrimidines en Route to 7-Formyl-1,3-Diazopyrenes
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.
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9778996/ https://www.ncbi.nlm.nih.gov/pubmed/36555299 http://dx.doi.org/10.3390/ijms232415657 |
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author | Shcherbakov, Stanislav V. Aksenov, Alexander V. Vendin, Maksim V. Shcherbakova, Viktoria Yu. Ivanova, Anna Yu. Shcheglov, Maksim O. Ovcharov, Sergei N. Rubin, Michael |
author_facet | Shcherbakov, Stanislav V. Aksenov, Alexander V. Vendin, Maksim V. Shcherbakova, Viktoria Yu. Ivanova, Anna Yu. Shcheglov, Maksim O. Ovcharov, Sergei N. Rubin, Michael |
author_sort | Shcherbakov, Stanislav V. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9778996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97789962022-12-23 Annulation of Perimidines with 5-Alkynylpyrimidines en Route to 7-Formyl-1,3-Diazopyrenes Shcherbakov, Stanislav V. Aksenov, Alexander V. Vendin, Maksim V. Shcherbakova, Viktoria Yu. Ivanova, Anna Yu. Shcheglov, Maksim O. Ovcharov, Sergei N. Rubin, Michael Int J Mol Sci Article 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. MDPI 2022-12-10 /pmc/articles/PMC9778996/ /pubmed/36555299 http://dx.doi.org/10.3390/ijms232415657 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Shcherbakov, Stanislav V. Aksenov, Alexander V. Vendin, Maksim V. Shcherbakova, Viktoria Yu. Ivanova, Anna Yu. Shcheglov, Maksim O. Ovcharov, Sergei N. Rubin, Michael Annulation of Perimidines with 5-Alkynylpyrimidines en Route to 7-Formyl-1,3-Diazopyrenes |
title | Annulation of Perimidines with 5-Alkynylpyrimidines en Route to 7-Formyl-1,3-Diazopyrenes |
title_full | Annulation of Perimidines with 5-Alkynylpyrimidines en Route to 7-Formyl-1,3-Diazopyrenes |
title_fullStr | Annulation of Perimidines with 5-Alkynylpyrimidines en Route to 7-Formyl-1,3-Diazopyrenes |
title_full_unstemmed | Annulation of Perimidines with 5-Alkynylpyrimidines en Route to 7-Formyl-1,3-Diazopyrenes |
title_short | Annulation of Perimidines with 5-Alkynylpyrimidines en Route to 7-Formyl-1,3-Diazopyrenes |
title_sort | annulation of perimidines with 5-alkynylpyrimidines en route to 7-formyl-1,3-diazopyrenes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9778996/ https://www.ncbi.nlm.nih.gov/pubmed/36555299 http://dx.doi.org/10.3390/ijms232415657 |
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