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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...

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Autores principales: Šterman, Andrej, Sosič, Izidor, Gobec, Stanislav, Časar, Zdenko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
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.
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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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