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Synthesis of 2,6-Dibromo-9-selenabicyclo[3.3.1]nonane-Based Pyridinium Salts Containing Acetal Groups
An efficient one-pot procedure has been developed for the synthesis of previously unknown 1,1′-(9-selenabicyclo[3.3.1]nonane-2,6-diyl)dipyridinium dibromides containing acetal moieties via transannular addition of selenium dibromide to Z,Z-cycloocta-1,5-diene, followed by reaction with pyridine-3-...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pleiades Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156833/ http://dx.doi.org/10.1134/S1070428022040236 |
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author | Musalov, M. V. Zhivet’eva, S. A. Shkurchenko, I. V. Amosova, S. V. Potapov, V. A. |
author_facet | Musalov, M. V. Zhivet’eva, S. A. Shkurchenko, I. V. Amosova, S. V. Potapov, V. A. |
author_sort | Musalov, M. V. |
collection | PubMed |
description | An efficient one-pot procedure has been developed for the synthesis of previously unknown 1,1′-(9-selenabicyclo[3.3.1]nonane-2,6-diyl)dipyridinium dibromides containing acetal moieties via transannular addition of selenium dibromide to Z,Z-cycloocta-1,5-diene, followed by reaction with pyridine-3- and 4-carbaldehyde acetals. The yields of the target products range from 80 to 97%. |
format | Online Article Text |
id | pubmed-9156833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Pleiades Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-91568332022-06-02 Synthesis of 2,6-Dibromo-9-selenabicyclo[3.3.1]nonane-Based Pyridinium Salts Containing Acetal Groups Musalov, M. V. Zhivet’eva, S. A. Shkurchenko, I. V. Amosova, S. V. Potapov, V. A. Russ J Org Chem Article An efficient one-pot procedure has been developed for the synthesis of previously unknown 1,1′-(9-selenabicyclo[3.3.1]nonane-2,6-diyl)dipyridinium dibromides containing acetal moieties via transannular addition of selenium dibromide to Z,Z-cycloocta-1,5-diene, followed by reaction with pyridine-3- and 4-carbaldehyde acetals. The yields of the target products range from 80 to 97%. Pleiades Publishing 2022-06-01 2022 /pmc/articles/PMC9156833/ http://dx.doi.org/10.1134/S1070428022040236 Text en © Pleiades Publishing, Ltd. 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Musalov, M. V. Zhivet’eva, S. A. Shkurchenko, I. V. Amosova, S. V. Potapov, V. A. Synthesis of 2,6-Dibromo-9-selenabicyclo[3.3.1]nonane-Based Pyridinium Salts Containing Acetal Groups |
title | Synthesis of 2,6-Dibromo-9-selenabicyclo[3.3.1]nonane-Based Pyridinium Salts Containing Acetal Groups |
title_full | Synthesis of 2,6-Dibromo-9-selenabicyclo[3.3.1]nonane-Based Pyridinium Salts Containing Acetal Groups |
title_fullStr | Synthesis of 2,6-Dibromo-9-selenabicyclo[3.3.1]nonane-Based Pyridinium Salts Containing Acetal Groups |
title_full_unstemmed | Synthesis of 2,6-Dibromo-9-selenabicyclo[3.3.1]nonane-Based Pyridinium Salts Containing Acetal Groups |
title_short | Synthesis of 2,6-Dibromo-9-selenabicyclo[3.3.1]nonane-Based Pyridinium Salts Containing Acetal Groups |
title_sort | synthesis of 2,6-dibromo-9-selenabicyclo[3.3.1]nonane-based pyridinium salts containing acetal groups |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9156833/ http://dx.doi.org/10.1134/S1070428022040236 |
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