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Transition metal catalyzed borylation of functional π-systems
Borylated functional π-systems are useful building blocks to enable efficient synthesis of novel molecular architectures with beautiful structures, intriguing properties and unique functions. Introduction of boronic ester substituents to a variety of extended π-systems can be achieved through either...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Japan Academy
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923104/ https://www.ncbi.nlm.nih.gov/pubmed/24492644 http://dx.doi.org/10.2183/pjab.90.1 |
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author | SHINOKUBO, Hiroshi |
author_facet | SHINOKUBO, Hiroshi |
author_sort | SHINOKUBO, Hiroshi |
collection | PubMed |
description | Borylated functional π-systems are useful building blocks to enable efficient synthesis of novel molecular architectures with beautiful structures, intriguing properties and unique functions. Introduction of boronic ester substituents to a variety of extended π-systems can be achieved through either iridium-catalyzed direct C–H borylation or the two-step procedure via electrophilic halogenation followed by palladium-catalyzed borylation. This review article focuses on our recent progress on borylation of large π-conjugated systems such as porphyrins, perylene bisimides, hexabenzocoronenes and dipyrrins. |
format | Online Article Text |
id | pubmed-3923104 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Japan Academy |
record_format | MEDLINE/PubMed |
spelling | pubmed-39231042014-03-04 Transition metal catalyzed borylation of functional π-systems SHINOKUBO, Hiroshi Proc Jpn Acad Ser B Phys Biol Sci Review Borylated functional π-systems are useful building blocks to enable efficient synthesis of novel molecular architectures with beautiful structures, intriguing properties and unique functions. Introduction of boronic ester substituents to a variety of extended π-systems can be achieved through either iridium-catalyzed direct C–H borylation or the two-step procedure via electrophilic halogenation followed by palladium-catalyzed borylation. This review article focuses on our recent progress on borylation of large π-conjugated systems such as porphyrins, perylene bisimides, hexabenzocoronenes and dipyrrins. The Japan Academy 2014-01-10 /pmc/articles/PMC3923104/ /pubmed/24492644 http://dx.doi.org/10.2183/pjab.90.1 Text en © 2014 The Japan Academy This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review SHINOKUBO, Hiroshi Transition metal catalyzed borylation of functional π-systems |
title | Transition metal catalyzed borylation of functional π-systems |
title_full | Transition metal catalyzed borylation of functional π-systems |
title_fullStr | Transition metal catalyzed borylation of functional π-systems |
title_full_unstemmed | Transition metal catalyzed borylation of functional π-systems |
title_short | Transition metal catalyzed borylation of functional π-systems |
title_sort | transition metal catalyzed borylation of functional π-systems |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923104/ https://www.ncbi.nlm.nih.gov/pubmed/24492644 http://dx.doi.org/10.2183/pjab.90.1 |
work_keys_str_mv | AT shinokubohiroshi transitionmetalcatalyzedborylationoffunctionalpsystems |