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Iron catalyzed methylation and ethylation of vinyl arenes

Short alkyl chain Heck (type) reactions, especially methyl Heck reactions, are a difficult aspect of the alkyl Heck reaction. To provide a solution to this problem, iron-catalyzed methyl, ethyl and propyl Heck reactions were developed using readily available alkyl peroxides as alkyl sources. The rea...

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Detalles Bibliográficos
Autores principales: Zhu, Nengbo, Zhao, Jianguo, Bao, Hongli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399631/
https://www.ncbi.nlm.nih.gov/pubmed/28451327
http://dx.doi.org/10.1039/c6sc04274k
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author Zhu, Nengbo
Zhao, Jianguo
Bao, Hongli
author_facet Zhu, Nengbo
Zhao, Jianguo
Bao, Hongli
author_sort Zhu, Nengbo
collection PubMed
description Short alkyl chain Heck (type) reactions, especially methyl Heck reactions, are a difficult aspect of the alkyl Heck reaction. To provide a solution to this problem, iron-catalyzed methyl, ethyl and propyl Heck reactions were developed using readily available alkyl peroxides as alkyl sources. The reaction conditions were mild, clean, and easy to handle. No additive was needed, and no hazardous waste was generated. The products were obtained in up to 99% yield of one isomer for most situations. This reaction works for many types of olefin and tolerates a variety of functional groups. Several late-stage functionalizations of natural products and drug molecules were conducted to demonstrate the synthetic applications of this reaction.
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spelling pubmed-53996312017-04-27 Iron catalyzed methylation and ethylation of vinyl arenes Zhu, Nengbo Zhao, Jianguo Bao, Hongli Chem Sci Chemistry Short alkyl chain Heck (type) reactions, especially methyl Heck reactions, are a difficult aspect of the alkyl Heck reaction. To provide a solution to this problem, iron-catalyzed methyl, ethyl and propyl Heck reactions were developed using readily available alkyl peroxides as alkyl sources. The reaction conditions were mild, clean, and easy to handle. No additive was needed, and no hazardous waste was generated. The products were obtained in up to 99% yield of one isomer for most situations. This reaction works for many types of olefin and tolerates a variety of functional groups. Several late-stage functionalizations of natural products and drug molecules were conducted to demonstrate the synthetic applications of this reaction. Royal Society of Chemistry 2017-03-01 2016-12-02 /pmc/articles/PMC5399631/ /pubmed/28451327 http://dx.doi.org/10.1039/c6sc04274k Text en This journal is © The Royal Society of Chemistry 2016 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Zhu, Nengbo
Zhao, Jianguo
Bao, Hongli
Iron catalyzed methylation and ethylation of vinyl arenes
title Iron catalyzed methylation and ethylation of vinyl arenes
title_full Iron catalyzed methylation and ethylation of vinyl arenes
title_fullStr Iron catalyzed methylation and ethylation of vinyl arenes
title_full_unstemmed Iron catalyzed methylation and ethylation of vinyl arenes
title_short Iron catalyzed methylation and ethylation of vinyl arenes
title_sort iron catalyzed methylation and ethylation of vinyl arenes
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399631/
https://www.ncbi.nlm.nih.gov/pubmed/28451327
http://dx.doi.org/10.1039/c6sc04274k
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AT zhaojianguo ironcatalyzedmethylationandethylationofvinylarenes
AT baohongli ironcatalyzedmethylationandethylationofvinylarenes