Professor Anita Mattson

Recent papers from the Mattson Group

Urea Activation of ?-Nitrodiazoesters: An Organocatalytic Approach to N?H Insertion Reactions

Arylation of Diazoesters by a Transient N?H Insertion Organocascade

Urea-Induced Acid Amplification: A New Approach for Metal-Free Insertion Chemistry

<h3>Professor Anita Mattson</h3>
<p>Boronate ureas benefit from internal Lewis acid coordination of the urea cabonyl oxygen and the strategically placed boron. As a result of this structural feature, boronate ureas can be rendered more acidic than conventional urea hydrogen bond donor catalysts. These more acidic boronate ureas are stable, storable, easy to use, and can enable enhanced and/or unique reactivity patterns when compared to conventional urea catalysts.<br>
<br>
<a href="https://www.amattson.com/" target="_blank">Mattson Group Website</a></p>


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<h2>DISCIPLINES</h2>
<ul>
<li>Organic Synthetic Chemistry</li>
<li>Catalysis</li>
</ul>
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Boronate ureas benefit from internal Lewis acid coordination of the urea cabonyl oxygen and the strategically placed boron. As a result of this structural feature, boronate ureas can be rendered more acidic than conventional urea hydrogen bond donor catalysts.