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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...

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Detalles Bibliográficos
Autores principales: Berger, Anna Lucia, Donabauer, Karsten, König, Burkhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
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.
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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
title_full Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones
title_fullStr Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones
title_full_unstemmed Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones
title_short Photocatalytic Barbier reaction – visible-light induced allylation and benzylation of aldehydes and ketones
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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AT konigburkhard photocatalyticbarbierreactionvisiblelightinducedallylationandbenzylationofaldehydesandketones