In this study, mono- or poly-methoxylated phenyl boronic acids, were subjected to Rieche formylation. Unexpectedly the corresponding ipso-substituted aryl aldehydes were obtained in excellent yields and, for some of these substrates, the formylated arylboronic acids were also synthesized in moderate yields. These findings provide new insights into the general reactivity and versatility of arylboronic acids.Mono- and poly-methoxylated phenyl boronic acids were subjected to Rieche formylation, the corresponding i pso-substituted aryl aldehydes or the formylated arylboronic acids were prepared with good to excellent yields.image

Reactivity Insights of Methoxyphenyl Boronic Acids in Rieche Formylation Reaction / Santarsiere, Alessandro; Funicello, Maria; Lupattelli, Paolo; Choppin, Sabine; Colobert, Françoise; Hanquet, Gilles; Chiummiento, Lucia. - In: CHEMISTRYSELECT. - ISSN 2365-6549. - 8:34(2023), pp. 1-5. [10.1002/slct.202302100]

Reactivity Insights of Methoxyphenyl Boronic Acids in Rieche Formylation Reaction

Lupattelli, Paolo;
2023

Abstract

In this study, mono- or poly-methoxylated phenyl boronic acids, were subjected to Rieche formylation. Unexpectedly the corresponding ipso-substituted aryl aldehydes were obtained in excellent yields and, for some of these substrates, the formylated arylboronic acids were also synthesized in moderate yields. These findings provide new insights into the general reactivity and versatility of arylboronic acids.Mono- and poly-methoxylated phenyl boronic acids were subjected to Rieche formylation, the corresponding i pso-substituted aryl aldehydes or the formylated arylboronic acids were prepared with good to excellent yields.image
2023
benzaldehyde derivatives; electron-rich arylboronic acids; formylated boronic acids; Lewis acid; Rieche formylation
01 Pubblicazione su rivista::01a Articolo in rivista
Reactivity Insights of Methoxyphenyl Boronic Acids in Rieche Formylation Reaction / Santarsiere, Alessandro; Funicello, Maria; Lupattelli, Paolo; Choppin, Sabine; Colobert, Françoise; Hanquet, Gilles; Chiummiento, Lucia. - In: CHEMISTRYSELECT. - ISSN 2365-6549. - 8:34(2023), pp. 1-5. [10.1002/slct.202302100]
File allegati a questo prodotto
File Dimensione Formato  
Santarsiere-Reactivity_2023.pdf

accesso aperto

Tipologia: Versione editoriale (versione pubblicata con il layout dell'editore)
Licenza: Tutti i diritti riservati (All rights reserved)
Dimensione 2.32 MB
Formato Adobe PDF
2.32 MB Adobe PDF

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1714113
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 0
  • ???jsp.display-item.citation.isi??? 0
social impact