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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...

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Autores principales: Yang, Ping, Zheng, Chao, Nie, Yu-Han, You, Shu-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2020
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.
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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
title_full Palladium-catalyzed dearomative 1,4-difunctionalization of naphthalenes
title_fullStr Palladium-catalyzed dearomative 1,4-difunctionalization of naphthalenes
title_full_unstemmed Palladium-catalyzed dearomative 1,4-difunctionalization of naphthalenes
title_short Palladium-catalyzed dearomative 1,4-difunctionalization of naphthalenes
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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