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.imageFile | Dimensione | Formato | |
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