Synthesis of α‐Aryl Esters and Nitriles: Deaminative Coupling of α‐Aminoesters and α‐Aminoacetonitriles with Arylboronic Acids |
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Authors: | Guojiao Wu Yifan Deng Chaoqiang Wu Dr. Yan Zhang Prof. Dr. Jianbo Wang |
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Affiliation: | 1. Beijing National Laboratory of Molecular Sciences (BNLMS) and Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871 (China);2. The State Key Laboratory of Organometallic Chemistry, Chinese Academy of Sciences, Shanghai 200032 (China) |
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Abstract: | Transition‐metal‐free synthesis of α‐aryl esters and nitriles using arylboronic acids with α‐aminoesters and α‐aminoacetonitriles, respectively, as the starting materials has been developed. The reaction represents a rare case of converting C(sp3)? N bonds into C(sp3)? C(sp2) bonds. The reaction conditions are mild, demonstrate good functional‐group tolerance, and can be scaled up. |
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Keywords: | arenes boron diazo compounds nitriles synthetic methods |
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