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Tri(boryl)alkanes and Tri(boryl)alkenes: The Versatile Reagents
The interest of organoboron chemistry in organic synthesis is growing, together with the development of new and versatile polyborated reagents. Here, the preparation of 1,1,1-tri(boryl)alkanes, 1,2,3-tri(boryl)alkanes, 1,1,2-tri(boryl)alkanes, as well as 1,1,2-tri(boryl)alkenes as suitable and acces...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7180881/ https://www.ncbi.nlm.nih.gov/pubmed/32290330 http://dx.doi.org/10.3390/molecules25071758 |
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author | Salvadó, Oriol Fernández, Elena |
author_facet | Salvadó, Oriol Fernández, Elena |
author_sort | Salvadó, Oriol |
collection | PubMed |
description | The interest of organoboron chemistry in organic synthesis is growing, together with the development of new and versatile polyborated reagents. Here, the preparation of 1,1,1-tri(boryl)alkanes, 1,2,3-tri(boryl)alkanes, 1,1,2-tri(boryl)alkanes, as well as 1,1,2-tri(boryl)alkenes as suitable and accessible polyborated systems is demonstrated as being easily applied in the construction of new carbon-carbon and carbon-heteroatom bonds. Synthetic procedures and limitations have been collected to demonstrate the powerful strategies to construct selective molecules, taking advantages of the easy transformation of carbon-boron bond in multiple functionalities, under the total control of chemo- and stereoselectivity. |
format | Online Article Text |
id | pubmed-7180881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71808812020-05-01 Tri(boryl)alkanes and Tri(boryl)alkenes: The Versatile Reagents Salvadó, Oriol Fernández, Elena Molecules Review The interest of organoboron chemistry in organic synthesis is growing, together with the development of new and versatile polyborated reagents. Here, the preparation of 1,1,1-tri(boryl)alkanes, 1,2,3-tri(boryl)alkanes, 1,1,2-tri(boryl)alkanes, as well as 1,1,2-tri(boryl)alkenes as suitable and accessible polyborated systems is demonstrated as being easily applied in the construction of new carbon-carbon and carbon-heteroatom bonds. Synthetic procedures and limitations have been collected to demonstrate the powerful strategies to construct selective molecules, taking advantages of the easy transformation of carbon-boron bond in multiple functionalities, under the total control of chemo- and stereoselectivity. MDPI 2020-04-10 /pmc/articles/PMC7180881/ /pubmed/32290330 http://dx.doi.org/10.3390/molecules25071758 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Salvadó, Oriol Fernández, Elena Tri(boryl)alkanes and Tri(boryl)alkenes: The Versatile Reagents |
title | Tri(boryl)alkanes and Tri(boryl)alkenes: The Versatile Reagents |
title_full | Tri(boryl)alkanes and Tri(boryl)alkenes: The Versatile Reagents |
title_fullStr | Tri(boryl)alkanes and Tri(boryl)alkenes: The Versatile Reagents |
title_full_unstemmed | Tri(boryl)alkanes and Tri(boryl)alkenes: The Versatile Reagents |
title_short | Tri(boryl)alkanes and Tri(boryl)alkenes: The Versatile Reagents |
title_sort | tri(boryl)alkanes and tri(boryl)alkenes: the versatile reagents |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7180881/ https://www.ncbi.nlm.nih.gov/pubmed/32290330 http://dx.doi.org/10.3390/molecules25071758 |
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