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喹啉的合成:钯催化的α-氨基肉桂腈与芳基肼的脱氮级联反应

The synthesis of quinolines denitrogenative palladium-catalyzed cascade reaction of -aminocinnamonitriles with arylhydrazines.

作者信息

Xie Jing, Huang Hang, Xu Tong, Li Renhao, Chen Jiuxi, Ye Xueting

机构信息

Department of Stomatology, The First Affiliated Hospital of Wenzhou Medical University Wenzhou 325000 China.

Department of Urology, The First Affiliated Hospital of Wenzhou Medical University Wenzhou 325000 China

出版信息

RSC Adv. 2020 Mar 3;10(15):8586-8593. doi: 10.1039/d0ra01043j. eCollection 2020 Feb 27.

Abstract

The first example of the palladium-catalyzed cascade reaction of -aminocinnamonitriles with arylhydrazines has been achieved, providing an efficient synthetic pathway to access quinolines with moderate to good yields. Preliminary mechanistic experiments indicate that this cascade process involves sequential denitrogenative addition followed by an intramolecular cyclization.

摘要

实现了钯催化的α-氨基肉桂腈与芳基肼的串联反应的首例报道,为以中等至良好产率获得喹啉提供了一条有效的合成途径。初步机理实验表明,该串联过程涉及依次的脱氮加成,随后是分子内环化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3240/9050002/eb0aecdd1c56/d0ra01043j-f1.jpg

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