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Palladium-catalyzed dearomative 1,4-difunctionalization of naphthalenes
A highly diastereoselective dearomatization of naphthalenes via a Pd-catalyzed 1,4-difunctionalization reaction is described. In the presence of a commercially available palladium precursor and ligand, intramolecular dearomative Heck-type insertion provides π-allylpalladium intermediates which are r...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7504896/ https://www.ncbi.nlm.nih.gov/pubmed/33033598 http://dx.doi.org/10.1039/d0sc02816a |
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author | Yang, Ping Zheng, Chao Nie, Yu-Han You, Shu-Li |
author_facet | Yang, Ping Zheng, Chao Nie, Yu-Han You, Shu-Li |
author_sort | Yang, Ping |
collection | PubMed |
description | A highly diastereoselective dearomatization of naphthalenes via a Pd-catalyzed 1,4-difunctionalization reaction is described. In the presence of a commercially available palladium precursor and ligand, intramolecular dearomative Heck-type insertion provides π-allylpalladium intermediates which are readily captured by a series of nucleophiles in excellent yields (up to 99%). This reaction features mild conditions, broad substrate scope, and useful transformations of the products. |
format | Online Article Text |
id | pubmed-7504896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-75048962020-10-07 Palladium-catalyzed dearomative 1,4-difunctionalization of naphthalenes Yang, Ping Zheng, Chao Nie, Yu-Han You, Shu-Li Chem Sci Chemistry A highly diastereoselective dearomatization of naphthalenes via a Pd-catalyzed 1,4-difunctionalization reaction is described. In the presence of a commercially available palladium precursor and ligand, intramolecular dearomative Heck-type insertion provides π-allylpalladium intermediates which are readily captured by a series of nucleophiles in excellent yields (up to 99%). This reaction features mild conditions, broad substrate scope, and useful transformations of the products. Royal Society of Chemistry 2020-06-10 /pmc/articles/PMC7504896/ /pubmed/33033598 http://dx.doi.org/10.1039/d0sc02816a Text en This journal is © The Royal Society of Chemistry 2020 https://creativecommons.org/licenses/by/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Yang, Ping Zheng, Chao Nie, Yu-Han You, Shu-Li Palladium-catalyzed dearomative 1,4-difunctionalization of naphthalenes |
title | Palladium-catalyzed dearomative 1,4-difunctionalization of naphthalenes
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title_full | Palladium-catalyzed dearomative 1,4-difunctionalization of naphthalenes
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title_fullStr | Palladium-catalyzed dearomative 1,4-difunctionalization of naphthalenes
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title_full_unstemmed | Palladium-catalyzed dearomative 1,4-difunctionalization of naphthalenes
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title_short | Palladium-catalyzed dearomative 1,4-difunctionalization of naphthalenes
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title_sort | palladium-catalyzed dearomative 1,4-difunctionalization of naphthalenes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7504896/ https://www.ncbi.nlm.nih.gov/pubmed/33033598 http://dx.doi.org/10.1039/d0sc02816a |
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