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Metal-free thermal organocatalytic pinacol coupling of arylaldehydes using an isonicotinate catalyst with bis(pinacolato)diboron

The metal-free thermal organocatalytic pinacol coupling of arylaldehydes has been developed. The intermolecular coupling of arylaldehydes catalyzed by t-butyl isonicotinate with bis(pinacolato)diboron as the co-reducing agent afforded 1,2-diphenylethane-1,2-diols. This reaction was also applicable t...

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Detalles Bibliográficos
Autores principales: Yasui, Masamichi, Hanaya, Kengo, Sugai, Takeshi, Higashibayashi, Shuhei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036917/
https://www.ncbi.nlm.nih.gov/pubmed/35481014
http://dx.doi.org/10.1039/d1ra04443e
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author Yasui, Masamichi
Hanaya, Kengo
Sugai, Takeshi
Higashibayashi, Shuhei
author_facet Yasui, Masamichi
Hanaya, Kengo
Sugai, Takeshi
Higashibayashi, Shuhei
author_sort Yasui, Masamichi
collection PubMed
description The metal-free thermal organocatalytic pinacol coupling of arylaldehydes has been developed. The intermolecular coupling of arylaldehydes catalyzed by t-butyl isonicotinate with bis(pinacolato)diboron as the co-reducing agent afforded 1,2-diphenylethane-1,2-diols. This reaction was also applicable to the intramolecular coupling of 1,1′-biphenyl-2,2′-dicarbaldehydes to afford 9,10-dihydrophenanthrene-9,10-diols. Various functional groups were tolerated under this coupling condition.
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spelling pubmed-90369172022-04-26 Metal-free thermal organocatalytic pinacol coupling of arylaldehydes using an isonicotinate catalyst with bis(pinacolato)diboron Yasui, Masamichi Hanaya, Kengo Sugai, Takeshi Higashibayashi, Shuhei RSC Adv Chemistry The metal-free thermal organocatalytic pinacol coupling of arylaldehydes has been developed. The intermolecular coupling of arylaldehydes catalyzed by t-butyl isonicotinate with bis(pinacolato)diboron as the co-reducing agent afforded 1,2-diphenylethane-1,2-diols. This reaction was also applicable to the intramolecular coupling of 1,1′-biphenyl-2,2′-dicarbaldehydes to afford 9,10-dihydrophenanthrene-9,10-diols. Various functional groups were tolerated under this coupling condition. The Royal Society of Chemistry 2021-07-14 /pmc/articles/PMC9036917/ /pubmed/35481014 http://dx.doi.org/10.1039/d1ra04443e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Yasui, Masamichi
Hanaya, Kengo
Sugai, Takeshi
Higashibayashi, Shuhei
Metal-free thermal organocatalytic pinacol coupling of arylaldehydes using an isonicotinate catalyst with bis(pinacolato)diboron
title Metal-free thermal organocatalytic pinacol coupling of arylaldehydes using an isonicotinate catalyst with bis(pinacolato)diboron
title_full Metal-free thermal organocatalytic pinacol coupling of arylaldehydes using an isonicotinate catalyst with bis(pinacolato)diboron
title_fullStr Metal-free thermal organocatalytic pinacol coupling of arylaldehydes using an isonicotinate catalyst with bis(pinacolato)diboron
title_full_unstemmed Metal-free thermal organocatalytic pinacol coupling of arylaldehydes using an isonicotinate catalyst with bis(pinacolato)diboron
title_short Metal-free thermal organocatalytic pinacol coupling of arylaldehydes using an isonicotinate catalyst with bis(pinacolato)diboron
title_sort metal-free thermal organocatalytic pinacol coupling of arylaldehydes using an isonicotinate catalyst with bis(pinacolato)diboron
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036917/
https://www.ncbi.nlm.nih.gov/pubmed/35481014
http://dx.doi.org/10.1039/d1ra04443e
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