First synthesis of 4-(arylsulfonyl)phenols by regioselective [3+3] cyclocondensations of 1,3-bis(silyloxy)-1,3-butadienes with 2-arylsulfonyl-3-ethoxy-2-en-1-ones

The formal [3+3] cyclization of 1,3-bis(silyloxy)-1,3-butadienes with readily available 2-arylsulfonyl-3-ethoxy-2-en-1-ones resulted in regioselective formation of 4-(arylsulfonyl)phenols.

Detalles Bibliográficos
Autores principales: Riahi, Abdolmajid, Shkoor, Mohanad, Fatunsin, Olumide, Lubbe, Mathias, Reinke, Helmut, Langer, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2009
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111812/
https://www.ncbi.nlm.nih.gov/pubmed/32287440
http://dx.doi.org/10.1016/j.tetlet.2008.10.097
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author Riahi, Abdolmajid
Shkoor, Mohanad
Fatunsin, Olumide
Lubbe, Mathias
Reinke, Helmut
Langer, Peter
author_facet Riahi, Abdolmajid
Shkoor, Mohanad
Fatunsin, Olumide
Lubbe, Mathias
Reinke, Helmut
Langer, Peter
author_sort Riahi, Abdolmajid
collection PubMed
description The formal [3+3] cyclization of 1,3-bis(silyloxy)-1,3-butadienes with readily available 2-arylsulfonyl-3-ethoxy-2-en-1-ones resulted in regioselective formation of 4-(arylsulfonyl)phenols.
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spelling pubmed-71118122020-04-02 First synthesis of 4-(arylsulfonyl)phenols by regioselective [3+3] cyclocondensations of 1,3-bis(silyloxy)-1,3-butadienes with 2-arylsulfonyl-3-ethoxy-2-en-1-ones Riahi, Abdolmajid Shkoor, Mohanad Fatunsin, Olumide Lubbe, Mathias Reinke, Helmut Langer, Peter Tetrahedron Lett Article The formal [3+3] cyclization of 1,3-bis(silyloxy)-1,3-butadienes with readily available 2-arylsulfonyl-3-ethoxy-2-en-1-ones resulted in regioselective formation of 4-(arylsulfonyl)phenols. Elsevier Ltd. 2009-01-07 2008-11-01 /pmc/articles/PMC7111812/ /pubmed/32287440 http://dx.doi.org/10.1016/j.tetlet.2008.10.097 Text en Copyright © 2008 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Riahi, Abdolmajid
Shkoor, Mohanad
Fatunsin, Olumide
Lubbe, Mathias
Reinke, Helmut
Langer, Peter
First synthesis of 4-(arylsulfonyl)phenols by regioselective [3+3] cyclocondensations of 1,3-bis(silyloxy)-1,3-butadienes with 2-arylsulfonyl-3-ethoxy-2-en-1-ones
title First synthesis of 4-(arylsulfonyl)phenols by regioselective [3+3] cyclocondensations of 1,3-bis(silyloxy)-1,3-butadienes with 2-arylsulfonyl-3-ethoxy-2-en-1-ones
title_full First synthesis of 4-(arylsulfonyl)phenols by regioselective [3+3] cyclocondensations of 1,3-bis(silyloxy)-1,3-butadienes with 2-arylsulfonyl-3-ethoxy-2-en-1-ones
title_fullStr First synthesis of 4-(arylsulfonyl)phenols by regioselective [3+3] cyclocondensations of 1,3-bis(silyloxy)-1,3-butadienes with 2-arylsulfonyl-3-ethoxy-2-en-1-ones
title_full_unstemmed First synthesis of 4-(arylsulfonyl)phenols by regioselective [3+3] cyclocondensations of 1,3-bis(silyloxy)-1,3-butadienes with 2-arylsulfonyl-3-ethoxy-2-en-1-ones
title_short First synthesis of 4-(arylsulfonyl)phenols by regioselective [3+3] cyclocondensations of 1,3-bis(silyloxy)-1,3-butadienes with 2-arylsulfonyl-3-ethoxy-2-en-1-ones
title_sort first synthesis of 4-(arylsulfonyl)phenols by regioselective [3+3] cyclocondensations of 1,3-bis(silyloxy)-1,3-butadienes with 2-arylsulfonyl-3-ethoxy-2-en-1-ones
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111812/
https://www.ncbi.nlm.nih.gov/pubmed/32287440
http://dx.doi.org/10.1016/j.tetlet.2008.10.097
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