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Visible light amination/Smiles cascade: access to phthalazine derivatives

We report the synthesis of various phthalazines via a new cascade reaction, initiated by visible light photocatalysis, involving a radical hydroamination reaction followed by a radical Smiles rearrangement. Phthalazine derivatives are obtained in high yields and from a broad scope readily accessible...

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Autores principales: Brachet, Etienne, Marzo, Leyre, Selkti, Mohamed, König, Burkhard, Belmont, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018559/
https://www.ncbi.nlm.nih.gov/pubmed/30155150
http://dx.doi.org/10.1039/c6sc01095d
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author Brachet, Etienne
Marzo, Leyre
Selkti, Mohamed
König, Burkhard
Belmont, Philippe
author_facet Brachet, Etienne
Marzo, Leyre
Selkti, Mohamed
König, Burkhard
Belmont, Philippe
author_sort Brachet, Etienne
collection PubMed
description We report the synthesis of various phthalazines via a new cascade reaction, initiated by visible light photocatalysis, involving a radical hydroamination reaction followed by a radical Smiles rearrangement. Phthalazine derivatives are obtained in high yields and from a broad scope readily accessible ortho-alkynylsulfonohydrazone precursors. The mild photoredox conditions ensure an excellent functional group tolerance. Application of this strategy to a one-pot protocol starting from the corresponding carbonyl compounds, and subsequent functionalization allow the rapid synthesis of structurally diverse structures.
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spelling pubmed-60185592018-08-28 Visible light amination/Smiles cascade: access to phthalazine derivatives Brachet, Etienne Marzo, Leyre Selkti, Mohamed König, Burkhard Belmont, Philippe Chem Sci Chemistry We report the synthesis of various phthalazines via a new cascade reaction, initiated by visible light photocatalysis, involving a radical hydroamination reaction followed by a radical Smiles rearrangement. Phthalazine derivatives are obtained in high yields and from a broad scope readily accessible ortho-alkynylsulfonohydrazone precursors. The mild photoredox conditions ensure an excellent functional group tolerance. Application of this strategy to a one-pot protocol starting from the corresponding carbonyl compounds, and subsequent functionalization allow the rapid synthesis of structurally diverse structures. Royal Society of Chemistry 2016-08-01 2016-05-06 /pmc/articles/PMC6018559/ /pubmed/30155150 http://dx.doi.org/10.1039/c6sc01095d Text en This journal is © The Royal Society of Chemistry 2016 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
Brachet, Etienne
Marzo, Leyre
Selkti, Mohamed
König, Burkhard
Belmont, Philippe
Visible light amination/Smiles cascade: access to phthalazine derivatives
title Visible light amination/Smiles cascade: access to phthalazine derivatives
title_full Visible light amination/Smiles cascade: access to phthalazine derivatives
title_fullStr Visible light amination/Smiles cascade: access to phthalazine derivatives
title_full_unstemmed Visible light amination/Smiles cascade: access to phthalazine derivatives
title_short Visible light amination/Smiles cascade: access to phthalazine derivatives
title_sort visible light amination/smiles cascade: access to phthalazine derivatives
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018559/
https://www.ncbi.nlm.nih.gov/pubmed/30155150
http://dx.doi.org/10.1039/c6sc01095d
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