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Synthesis of BN-Polyarenes by a Mild Borylative Cyclization Cascade
[Image: see text] Reaction of BCl(3) with suitably substituted o-alkynylanilines promotes a cascade reaction in which BN-polycyclic compounds are obtained via the formation of two new cycles and three new bonds in a single operational step. The reaction is highly efficient and takes place at room te...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9384698/ https://www.ncbi.nlm.nih.gov/pubmed/35913827 http://dx.doi.org/10.1021/acs.orglett.2c02477 |
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author | Sans-Panadés, Ester Vaquero, Juan J. Fernández-Rodríguez, Manuel A. García-García, Patricia |
author_facet | Sans-Panadés, Ester Vaquero, Juan J. Fernández-Rodríguez, Manuel A. García-García, Patricia |
author_sort | Sans-Panadés, Ester |
collection | PubMed |
description | [Image: see text] Reaction of BCl(3) with suitably substituted o-alkynylanilines promotes a cascade reaction in which BN-polycyclic compounds are obtained via the formation of two new cycles and three new bonds in a single operational step. The reaction is highly efficient and takes place at room temperature, providing a very mild and straightforward strategy for the preparation of BN-aromatic compounds, which can be further transformed into a variety of BN-PAHs with different polycyclic cores and substituents. |
format | Online Article Text |
id | pubmed-9384698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-93846982022-08-18 Synthesis of BN-Polyarenes by a Mild Borylative Cyclization Cascade Sans-Panadés, Ester Vaquero, Juan J. Fernández-Rodríguez, Manuel A. García-García, Patricia Org Lett [Image: see text] Reaction of BCl(3) with suitably substituted o-alkynylanilines promotes a cascade reaction in which BN-polycyclic compounds are obtained via the formation of two new cycles and three new bonds in a single operational step. The reaction is highly efficient and takes place at room temperature, providing a very mild and straightforward strategy for the preparation of BN-aromatic compounds, which can be further transformed into a variety of BN-PAHs with different polycyclic cores and substituents. American Chemical Society 2022-08-01 2022-08-12 /pmc/articles/PMC9384698/ /pubmed/35913827 http://dx.doi.org/10.1021/acs.orglett.2c02477 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Sans-Panadés, Ester Vaquero, Juan J. Fernández-Rodríguez, Manuel A. García-García, Patricia Synthesis of BN-Polyarenes by a Mild Borylative Cyclization Cascade |
title | Synthesis of
BN-Polyarenes by a Mild Borylative Cyclization
Cascade |
title_full | Synthesis of
BN-Polyarenes by a Mild Borylative Cyclization
Cascade |
title_fullStr | Synthesis of
BN-Polyarenes by a Mild Borylative Cyclization
Cascade |
title_full_unstemmed | Synthesis of
BN-Polyarenes by a Mild Borylative Cyclization
Cascade |
title_short | Synthesis of
BN-Polyarenes by a Mild Borylative Cyclization
Cascade |
title_sort | synthesis of
bn-polyarenes by a mild borylative cyclization
cascade |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9384698/ https://www.ncbi.nlm.nih.gov/pubmed/35913827 http://dx.doi.org/10.1021/acs.orglett.2c02477 |
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