Cargando…

Transition metal–catalyzed remote C─H borylation: An emerging synthetic tool

Transition metal–catalyzed C─H bond activation and borylation is a powerful synthetic method that offers versatile synthetic transformation from organoboron compounds to virtually all other functional groups. Compared to the ortho-borylation, remote borylation remains more challenging owing to the i...

Descripción completa

Detalles Bibliográficos
Autores principales: Hassan, Mirja Md Mahamudul, Guria, Saikat, Dey, Sayan, Das, Jaitri, Chattopadhyay, Buddhadeb
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10121176/
https://www.ncbi.nlm.nih.gov/pubmed/37083526
http://dx.doi.org/10.1126/sciadv.adg3311
_version_ 1785029327631417344
author Hassan, Mirja Md Mahamudul
Guria, Saikat
Dey, Sayan
Das, Jaitri
Chattopadhyay, Buddhadeb
author_facet Hassan, Mirja Md Mahamudul
Guria, Saikat
Dey, Sayan
Das, Jaitri
Chattopadhyay, Buddhadeb
author_sort Hassan, Mirja Md Mahamudul
collection PubMed
description Transition metal–catalyzed C─H bond activation and borylation is a powerful synthetic method that offers versatile synthetic transformation from organoboron compounds to virtually all other functional groups. Compared to the ortho-borylation, remote borylation remains more challenging owing to the inaccessibility of these C─H bonds. Enforcing the metal catalyst toward the remote C─H bonds needs well-judged catalyst design through proper ligand development. This review article aims to summarize the recent discoveries for the remote C─H borylation by the employment of new catalyst/ligand design with the help of steric of the ligand, noncovalent interactions. It has been found that C─H borylation now takes part in the total synthesis of natural products in a shorter route. Whereas, Ir-catalyzed C─H borylation is predominant, cobalt catalyst has also started to affect this field for sustainable and cost-effective development.
format Online
Article
Text
id pubmed-10121176
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher American Association for the Advancement of Science
record_format MEDLINE/PubMed
spelling pubmed-101211762023-04-22 Transition metal–catalyzed remote C─H borylation: An emerging synthetic tool Hassan, Mirja Md Mahamudul Guria, Saikat Dey, Sayan Das, Jaitri Chattopadhyay, Buddhadeb Sci Adv Physical and Materials Sciences Transition metal–catalyzed C─H bond activation and borylation is a powerful synthetic method that offers versatile synthetic transformation from organoboron compounds to virtually all other functional groups. Compared to the ortho-borylation, remote borylation remains more challenging owing to the inaccessibility of these C─H bonds. Enforcing the metal catalyst toward the remote C─H bonds needs well-judged catalyst design through proper ligand development. This review article aims to summarize the recent discoveries for the remote C─H borylation by the employment of new catalyst/ligand design with the help of steric of the ligand, noncovalent interactions. It has been found that C─H borylation now takes part in the total synthesis of natural products in a shorter route. Whereas, Ir-catalyzed C─H borylation is predominant, cobalt catalyst has also started to affect this field for sustainable and cost-effective development. American Association for the Advancement of Science 2023-04-21 /pmc/articles/PMC10121176/ /pubmed/37083526 http://dx.doi.org/10.1126/sciadv.adg3311 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Physical and Materials Sciences
Hassan, Mirja Md Mahamudul
Guria, Saikat
Dey, Sayan
Das, Jaitri
Chattopadhyay, Buddhadeb
Transition metal–catalyzed remote C─H borylation: An emerging synthetic tool
title Transition metal–catalyzed remote C─H borylation: An emerging synthetic tool
title_full Transition metal–catalyzed remote C─H borylation: An emerging synthetic tool
title_fullStr Transition metal–catalyzed remote C─H borylation: An emerging synthetic tool
title_full_unstemmed Transition metal–catalyzed remote C─H borylation: An emerging synthetic tool
title_short Transition metal–catalyzed remote C─H borylation: An emerging synthetic tool
title_sort transition metal–catalyzed remote c─h borylation: an emerging synthetic tool
topic Physical and Materials Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10121176/
https://www.ncbi.nlm.nih.gov/pubmed/37083526
http://dx.doi.org/10.1126/sciadv.adg3311
work_keys_str_mv AT hassanmirjamdmahamudul transitionmetalcatalyzedremotechborylationanemergingsynthetictool
AT guriasaikat transitionmetalcatalyzedremotechborylationanemergingsynthetictool
AT deysayan transitionmetalcatalyzedremotechborylationanemergingsynthetictool
AT dasjaitri transitionmetalcatalyzedremotechborylationanemergingsynthetictool
AT chattopadhyaybuddhadeb transitionmetalcatalyzedremotechborylationanemergingsynthetictool