Volume 36, Issue 8 p. 673
Cover Picture
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Cover Picture: Palladium-Catalyzed Intermolecular Oxidative Coupling Reactions of (Z)-Enamines with Isocyanides through Selective β-C(sp2)-H and/or C=C Bond Cleavage (Chin. J. Chem. 8/2018)

Weigao Hu

Weigao Hu

Key Lab of Functional Molecular Engineering of Guangdong Province, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, Guangdong, 510640 China

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Jia Zheng

Jia Zheng

Key Lab of Functional Molecular Engineering of Guangdong Province, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, Guangdong, 510640 China

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Meng Li

Meng Li

Key Lab of Functional Molecular Engineering of Guangdong Province, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, Guangdong, 510640 China

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Wanqing Wu

Wanqing Wu

Key Lab of Functional Molecular Engineering of Guangdong Province, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, Guangdong, 510640 China

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Haiyang Liu

Haiyang Liu

Key Lab of Functional Molecular Engineering of Guangdong Province, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, Guangdong, 510640 China

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Huanfeng Jiang

Corresponding Author

Huanfeng Jiang

Key Lab of Functional Molecular Engineering of Guangdong Province, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, Guangdong, 510640 China

E-mail: [email protected]Search for more papers by this author
First published: 13 July 2018

Abstract

The cover picture shows Two efficient intermolecular oxidative coupling reactions of (Z)-enamines with isocyanides via palladium catalysis have been developed. In these transformations, the β-C(sp2)-H and/or C = C bond were cut off selectively by using different anionic ligands, leading to controllable chemodivergent and stereoselective construction of a wide range of (E)β-carbamoylenamine derivatives with intramolecular hydrogen bonds. More details are discussed in the article by Jiang et al. on page 712–715.

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