A Metal‐Free Synthesis of N‐Aryl Carbamates under Ambient Conditions. (12th August 2015)

• Record Type: Journal Article
• Authors: Guo, Wusheng; Gónzalez‐Fabra, Joan; Bandeira, Nuno A. G.; Bo, Carles; Kleij, Arjan W.
• Is Part Of: Angewandte Chemie. Volume 127:Number 40(2015)
• Page Start: 11852
• Page End: 11856
• Publication Date: 2015-08-12
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201504956
• Languages: English
• ISSNs: 0044-8249

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The first chemo‐ and site‐selective process for the formation of N‐aryl‐carbamates from cyclic organic carbonates and aromatic amines is reported. The reactions proceed smoothly under extremely mild reaction conditions using TBD (triazabicyclodecene) as an effective and cheap organocatalyst, thus providing a sustainable and new methodology for the formation of a wide variety of useful N‐aryl carbamate synthons in good to excellent yields. Computational investigations have been performed and show the underlying reason for the observed unique reactivity as related to an effective proton‐relay mechanism mediated by the bicyclic guanidine base.</p> </abstract>