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Pd-catalyzed allylative dearomatisation using Grignard reagents
Pd-catalyzed allylative dearomatisation of naphthyl halides is shown to be feasible by employing Grignard reagents. The high reactivity of the nucleophile allows for fast reactions and low catalyst loading, while a plethora of successfully substituted compounds illustrate the broad scope. Five membe...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577247/ https://www.ncbi.nlm.nih.gov/pubmed/34693941 http://dx.doi.org/10.1039/d1cc05609c |
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author | Boldrini, Cosimo Harutyunyan, Syuzanna R. |
author_facet | Boldrini, Cosimo Harutyunyan, Syuzanna R. |
author_sort | Boldrini, Cosimo |
collection | PubMed |
description | Pd-catalyzed allylative dearomatisation of naphthyl halides is shown to be feasible by employing Grignard reagents. The high reactivity of the nucleophile allows for fast reactions and low catalyst loading, while a plethora of successfully substituted compounds illustrate the broad scope. Five membered heteroaromatic compounds are also demonstrated to be reactive under similar conditions. |
format | Online Article Text |
id | pubmed-8577247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-85772472021-12-13 Pd-catalyzed allylative dearomatisation using Grignard reagents Boldrini, Cosimo Harutyunyan, Syuzanna R. Chem Commun (Camb) Chemistry Pd-catalyzed allylative dearomatisation of naphthyl halides is shown to be feasible by employing Grignard reagents. The high reactivity of the nucleophile allows for fast reactions and low catalyst loading, while a plethora of successfully substituted compounds illustrate the broad scope. Five membered heteroaromatic compounds are also demonstrated to be reactive under similar conditions. The Royal Society of Chemistry 2021-10-25 /pmc/articles/PMC8577247/ /pubmed/34693941 http://dx.doi.org/10.1039/d1cc05609c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Boldrini, Cosimo Harutyunyan, Syuzanna R. Pd-catalyzed allylative dearomatisation using Grignard reagents |
title | Pd-catalyzed allylative dearomatisation using Grignard reagents |
title_full | Pd-catalyzed allylative dearomatisation using Grignard reagents |
title_fullStr | Pd-catalyzed allylative dearomatisation using Grignard reagents |
title_full_unstemmed | Pd-catalyzed allylative dearomatisation using Grignard reagents |
title_short | Pd-catalyzed allylative dearomatisation using Grignard reagents |
title_sort | pd-catalyzed allylative dearomatisation using grignard reagents |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577247/ https://www.ncbi.nlm.nih.gov/pubmed/34693941 http://dx.doi.org/10.1039/d1cc05609c |
work_keys_str_mv | AT boldrinicosimo pdcatalyzedallylativedearomatisationusinggrignardreagents AT harutyunyansyuzannar pdcatalyzedallylativedearomatisationusinggrignardreagents |