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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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Detalles Bibliográficos
Autor principal: SHINOKUBO, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Academy 2014
Materias:
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.
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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
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