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Substituents Regulate the Cyclization of Conjugated Alkynes to Accurately Construct Cyclo-(E)-[3]dendralenes
Substituent-regulated cyclization of conjugated alkynes with acid catalysis was developed in this paper, and it provides a straightforward synthesis of cyclic-(E)-[3]dendralenes. Depending on the electronic effect of the aromatic ring pairing, a variety of phosphinyl quintuplet/hexa cyclo-[3]dendral...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10254459/ https://www.ncbi.nlm.nih.gov/pubmed/37298858 http://dx.doi.org/10.3390/molecules28114382 |
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author | Xia, Yun-Tao Li, Ya-Xin Bi, Tong-Tong Lian, Wei Wang, Xia Yan, Meng Guo, Tao |
author_facet | Xia, Yun-Tao Li, Ya-Xin Bi, Tong-Tong Lian, Wei Wang, Xia Yan, Meng Guo, Tao |
author_sort | Xia, Yun-Tao |
collection | PubMed |
description | Substituent-regulated cyclization of conjugated alkynes with acid catalysis was developed in this paper, and it provides a straightforward synthesis of cyclic-(E)-[3]dendralenes. Depending on the electronic effect of the aromatic ring pairing, a variety of phosphinyl quintuplet/hexa cyclo-[3]dendralenes with diverse substitution patterns are accessible, with good efficiency and high stereoselectivity. This self-cyclization process achieves the first precise construction of a phosphinylcyclo-(E)-[3]dendralene from conjugated alkynes to aromatization. |
format | Online Article Text |
id | pubmed-10254459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102544592023-06-10 Substituents Regulate the Cyclization of Conjugated Alkynes to Accurately Construct Cyclo-(E)-[3]dendralenes Xia, Yun-Tao Li, Ya-Xin Bi, Tong-Tong Lian, Wei Wang, Xia Yan, Meng Guo, Tao Molecules Article Substituent-regulated cyclization of conjugated alkynes with acid catalysis was developed in this paper, and it provides a straightforward synthesis of cyclic-(E)-[3]dendralenes. Depending on the electronic effect of the aromatic ring pairing, a variety of phosphinyl quintuplet/hexa cyclo-[3]dendralenes with diverse substitution patterns are accessible, with good efficiency and high stereoselectivity. This self-cyclization process achieves the first precise construction of a phosphinylcyclo-(E)-[3]dendralene from conjugated alkynes to aromatization. MDPI 2023-05-27 /pmc/articles/PMC10254459/ /pubmed/37298858 http://dx.doi.org/10.3390/molecules28114382 Text en © 2023 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 Xia, Yun-Tao Li, Ya-Xin Bi, Tong-Tong Lian, Wei Wang, Xia Yan, Meng Guo, Tao Substituents Regulate the Cyclization of Conjugated Alkynes to Accurately Construct Cyclo-(E)-[3]dendralenes |
title | Substituents Regulate the Cyclization of Conjugated Alkynes to Accurately Construct Cyclo-(E)-[3]dendralenes |
title_full | Substituents Regulate the Cyclization of Conjugated Alkynes to Accurately Construct Cyclo-(E)-[3]dendralenes |
title_fullStr | Substituents Regulate the Cyclization of Conjugated Alkynes to Accurately Construct Cyclo-(E)-[3]dendralenes |
title_full_unstemmed | Substituents Regulate the Cyclization of Conjugated Alkynes to Accurately Construct Cyclo-(E)-[3]dendralenes |
title_short | Substituents Regulate the Cyclization of Conjugated Alkynes to Accurately Construct Cyclo-(E)-[3]dendralenes |
title_sort | substituents regulate the cyclization of conjugated alkynes to accurately construct cyclo-(e)-[3]dendralenes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10254459/ https://www.ncbi.nlm.nih.gov/pubmed/37298858 http://dx.doi.org/10.3390/molecules28114382 |
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