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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...

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Autores principales: Sans-Panadés, Ester, Vaquero, Juan J., Fernández-Rodríguez, Manuel A., García-García, Patricia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
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.
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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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