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Combining transition metals and transient directing groups for C–H functionalizations

In the domain of synthetic chemistry, C–H bond activation has always remained in the spotlight for researchers over the last few decades. Although different strategies have been employed to chemically trigger unactivated C–H bonds, transition metal catalyzed directing group (DG) aided C–H bond activ...

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Autores principales: Bhattacharya, Trisha, Pimparkar, Sandeep, Maiti, Debabrata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080754/
https://www.ncbi.nlm.nih.gov/pubmed/35541005
http://dx.doi.org/10.1039/c8ra03230k
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author Bhattacharya, Trisha
Pimparkar, Sandeep
Maiti, Debabrata
author_facet Bhattacharya, Trisha
Pimparkar, Sandeep
Maiti, Debabrata
author_sort Bhattacharya, Trisha
collection PubMed
description In the domain of synthetic chemistry, C–H bond activation has always remained in the spotlight for researchers over the last few decades. Although different strategies have been employed to chemically trigger unactivated C–H bonds, transition metal catalyzed directing group (DG) aided C–H bond activation is the most explored pathway of all because of its ability to perform diverse site selective functional metamorphosis. Despite its popularity, tedious synthetic methodology requiring additional steps for the installation and removal of DGs from the target substrate diminishes its efficacy. However, replacement of directing groups by transient directing groups (tDGs) reduces the hurdle to a greater extent without compromising the product yield and selectivity. In this report we have depicted the intense journey of transient directing groups with three (Rh, Ru, and Pd) prevalent second row transition metals.
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spelling pubmed-90807542022-05-09 Combining transition metals and transient directing groups for C–H functionalizations Bhattacharya, Trisha Pimparkar, Sandeep Maiti, Debabrata RSC Adv Chemistry In the domain of synthetic chemistry, C–H bond activation has always remained in the spotlight for researchers over the last few decades. Although different strategies have been employed to chemically trigger unactivated C–H bonds, transition metal catalyzed directing group (DG) aided C–H bond activation is the most explored pathway of all because of its ability to perform diverse site selective functional metamorphosis. Despite its popularity, tedious synthetic methodology requiring additional steps for the installation and removal of DGs from the target substrate diminishes its efficacy. However, replacement of directing groups by transient directing groups (tDGs) reduces the hurdle to a greater extent without compromising the product yield and selectivity. In this report we have depicted the intense journey of transient directing groups with three (Rh, Ru, and Pd) prevalent second row transition metals. The Royal Society of Chemistry 2018-05-29 /pmc/articles/PMC9080754/ /pubmed/35541005 http://dx.doi.org/10.1039/c8ra03230k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Bhattacharya, Trisha
Pimparkar, Sandeep
Maiti, Debabrata
Combining transition metals and transient directing groups for C–H functionalizations
title Combining transition metals and transient directing groups for C–H functionalizations
title_full Combining transition metals and transient directing groups for C–H functionalizations
title_fullStr Combining transition metals and transient directing groups for C–H functionalizations
title_full_unstemmed Combining transition metals and transient directing groups for C–H functionalizations
title_short Combining transition metals and transient directing groups for C–H functionalizations
title_sort combining transition metals and transient directing groups for c–h functionalizations
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080754/
https://www.ncbi.nlm.nih.gov/pubmed/35541005
http://dx.doi.org/10.1039/c8ra03230k
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