Reactivity Insights of Methoxyphenyl Boronic Acids in Rieche Formylation Reaction

Author:

Santarsiere Alessandro12,Funicello Maria1,Lupattelli Paolo3,Choppin Sabine2,Colobert Françoise2,Hanquet Gilles2,Chiummiento Lucia1ORCID

Affiliation:

1. Department of Science University of Basilicata Via dell'Ateneo lucano 10 85100 Potenza Italy

2. CNRS UMR 7042-LIMA ECPM Université de Strasbourg Université de Haute-Alsace Rue de Bequerel 67000 Strasbourg France

3. Department of Chemistry University “La Sapienza” of Roma Piazzale A. Moro 4 Roma Italy

Abstract

AbstractIn 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.

Funder

Università degli Studi della Basilicata

Publisher

Wiley

Subject

General Chemistry

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