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Recent Advances in the Synthesis of Acylboranes and Their Widening Applicability
[Image: see text] The most common types of acylboranes are acyltrifluoroborates, acyl MIDA-boronates, and monofluoroacylboronates. Because of the increasing importance of these compounds in the past decade, we highlight the recently reported synthetic strategies to access acylboranes. In addition, a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391254/ https://www.ncbi.nlm.nih.gov/pubmed/32743157 http://dx.doi.org/10.1021/acsomega.0c02391 |
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author | Šterman, Andrej Sosič, Izidor Gobec, Stanislav Časar, Zdenko |
author_facet | Šterman, Andrej Sosič, Izidor Gobec, Stanislav Časar, Zdenko |
author_sort | Šterman, Andrej |
collection | PubMed |
description | [Image: see text] The most common types of acylboranes are acyltrifluoroborates, acyl MIDA-boronates, and monofluoroacylboronates. Because of the increasing importance of these compounds in the past decade, we highlight the recently reported synthetic strategies to access acylboranes. In addition, an expanding array of their applications has been discovered, based on either the ability of acylboranes to enter rapid amide-forming ligations or the retained ketone-like character of the carbonyl group. Therefore, we also describe ground-breaking achievements where acylboranes were successfully put to use, such as their utility in biochemical, material, and medicinal sciences. |
format | Online Article Text |
id | pubmed-7391254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-73912542020-07-31 Recent Advances in the Synthesis of Acylboranes and Their Widening Applicability Šterman, Andrej Sosič, Izidor Gobec, Stanislav Časar, Zdenko ACS Omega [Image: see text] The most common types of acylboranes are acyltrifluoroborates, acyl MIDA-boronates, and monofluoroacylboronates. Because of the increasing importance of these compounds in the past decade, we highlight the recently reported synthetic strategies to access acylboranes. In addition, an expanding array of their applications has been discovered, based on either the ability of acylboranes to enter rapid amide-forming ligations or the retained ketone-like character of the carbonyl group. Therefore, we also describe ground-breaking achievements where acylboranes were successfully put to use, such as their utility in biochemical, material, and medicinal sciences. American Chemical Society 2020-07-14 /pmc/articles/PMC7391254/ /pubmed/32743157 http://dx.doi.org/10.1021/acsomega.0c02391 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Šterman, Andrej Sosič, Izidor Gobec, Stanislav Časar, Zdenko Recent Advances in the Synthesis of Acylboranes and Their Widening Applicability |
title | Recent Advances in the Synthesis
of Acylboranes and Their Widening
Applicability |
title_full | Recent Advances in the Synthesis
of Acylboranes and Their Widening
Applicability |
title_fullStr | Recent Advances in the Synthesis
of Acylboranes and Their Widening
Applicability |
title_full_unstemmed | Recent Advances in the Synthesis
of Acylboranes and Their Widening
Applicability |
title_short | Recent Advances in the Synthesis
of Acylboranes and Their Widening
Applicability |
title_sort | recent advances in the synthesis
of acylboranes and their widening
applicability |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391254/ https://www.ncbi.nlm.nih.gov/pubmed/32743157 http://dx.doi.org/10.1021/acsomega.0c02391 |
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