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Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones
We report a photocatalytic version of the Barbier type reaction using readily available allyl or benzyl bromides and aromatic aldehydes or ketones as starting materials to generate allylic or benzylic alcohols. The reaction proceeds at room temperature under visible light irradiation with the organi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148494/ https://www.ncbi.nlm.nih.gov/pubmed/30288242 http://dx.doi.org/10.1039/c8sc02038h |
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author | Berger, Anna Lucia Donabauer, Karsten König, Burkhard |
author_facet | Berger, Anna Lucia Donabauer, Karsten König, Burkhard |
author_sort | Berger, Anna Lucia |
collection | PubMed |
description | We report a photocatalytic version of the Barbier type reaction using readily available allyl or benzyl bromides and aromatic aldehydes or ketones as starting materials to generate allylic or benzylic alcohols. The reaction proceeds at room temperature under visible light irradiation with the organic dye 3,7-di(4-biphenyl)1-naphthalene-10-phenoxazine as a photocatalyst and DIPEA as sacrificial electron donor. The proposed cross-coupling mechanism of a ketyl- and an allyl or benzyl radical is supported by spectroscopic investigations and cyclic voltammetry measurements. |
format | Online Article Text |
id | pubmed-6148494 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-61484942018-10-04 Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones Berger, Anna Lucia Donabauer, Karsten König, Burkhard Chem Sci Chemistry We report a photocatalytic version of the Barbier type reaction using readily available allyl or benzyl bromides and aromatic aldehydes or ketones as starting materials to generate allylic or benzylic alcohols. The reaction proceeds at room temperature under visible light irradiation with the organic dye 3,7-di(4-biphenyl)1-naphthalene-10-phenoxazine as a photocatalyst and DIPEA as sacrificial electron donor. The proposed cross-coupling mechanism of a ketyl- and an allyl or benzyl radical is supported by spectroscopic investigations and cyclic voltammetry measurements. Royal Society of Chemistry 2018-08-02 /pmc/articles/PMC6148494/ /pubmed/30288242 http://dx.doi.org/10.1039/c8sc02038h Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Berger, Anna Lucia Donabauer, Karsten König, Burkhard Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones |
title | Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones
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title_full | Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones
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title_fullStr | Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones
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title_full_unstemmed | Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones
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title_short | Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones
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title_sort | photocatalytic barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148494/ https://www.ncbi.nlm.nih.gov/pubmed/30288242 http://dx.doi.org/10.1039/c8sc02038h |
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