Volume 58, Issue 7 p. 1850
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Inside Cover: Access to N-Substituted 2-Pyridones by Catalytic Intermolecular Dearomatization and 1,4-Acyl Transfer (Angew. Chem. Int. Ed. 7/2019)

Guangyang Xu

Guangyang Xu

Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering, Changzhou University, 1 Gehu Road, 213164 Changzhou, China

These authors contributed equally to this work.

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Ping Chen

Ping Chen

Lab of Computational Chemistry and Drug Design, State Key Laboratory of Chemical Oncogeomics, Peking University Shenzhen Graduate School, Shenzhen, 518055 China

These authors contributed equally to this work.

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Pei Liu

Pei Liu

Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering, Changzhou University, 1 Gehu Road, 213164 Changzhou, China

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Shengbiao Tang

Shengbiao Tang

Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering, Changzhou University, 1 Gehu Road, 213164 Changzhou, China

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Prof. Dr. Xinhao Zhang

Corresponding Author

Prof. Dr. Xinhao Zhang

Lab of Computational Chemistry and Drug Design, State Key Laboratory of Chemical Oncogeomics, Peking University Shenzhen Graduate School, Shenzhen, 518055 China

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Prof. Dr. Jiangtao Sun

Corresponding Author

Prof. Dr. Jiangtao Sun

Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering, Changzhou University, 1 Gehu Road, 213164 Changzhou, China

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First published: 16 January 2019
Citations: 1

Graphical Abstract

When the fearless Don Quixote was charging at windmills, he left his slow companion, Sancho Panza, behind. In their Communication on page 1980 ff., X. Zhang, J. Sun et al. describe a novel rhodium-catalyzed dearomatization and rearrangement of O-substituted pyridines to access N-substituted 2-pyridones, a challenging target because their straightforward synthesis by simple alkylation of 2-pyridones is thwarted by their preferred O-reactivity. The key to this transformation is the formation of the pyridinium ylide and a subsequent 1,4-acyl migratory rearrangement.

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