Abstract
AbstractWe performed direct carbamoylation using heteropoly acid (HPA) photocatalysts with a Keggin structure under UV‐light. Carbamoyl radicals were generated via the decarboxylation of N,N‐disubstituted dimethyloxamic acid under these conditions. The HPA catalyst functioned as a photocatalyst when the dicarbonyl bond was broken, generating carbon dioxide. We found that disubstituted carbamoyl radicals readily coupled with aromatic bromides to generate diverse benzoic amides. In particular, using a homogeneous HPA photocatalyst improved the reaction's transmittance, which had been a problem of the existing heterogeneous photocatalyst. This reaction condition can be easily handled, mild, and safer than the traditional benzoic amide synthesis. This method can be scaled up efficiently, is eco‐friendly, and can be applied to producing active pharmaceutical ingredients.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
