Remote Construction of Diverse Heteropolycycles via 1,4‐Pd or 1,4/1,5‐Pd Migration‐Mediated Intermolecular Double C–H Annulation

Comprehensive Summary Although 1,4‐Pd migration has been widely used for the functionalization of remote C−H bonds, intermolecular double C−H annulation via this strategy remains elusive. Furthermore, catalytic reactions involving 1,5‐Pd migration are scarce due to competitive reductive elimination pathway. Herein, we report an intermolecular double C–H annulation of N ‐(2‐bromophenyl)‐2‐phenylacrylamides with 1, n ‐diynes mediated by 1,4‐Pd or sequential 1,4/1,5‐Pd migrations. The reaction proceeds through sequential Heck cyclization, alkyl‐to‐aryl 1,4‐Pd migration (or alkyl‐to‐aryl 1,4‐Pd migration followed by aryl‐to‐aryl 1,5‐Pd migration), dual alkyne insertion, and C–H activation, providing efficient access to both indolinone‐substituted tricyclic frameworks and tetracyclic indolinones. The method exhibits excellent regioselectivity, and preliminary mechanistic studies support the proposed pathway.

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Publication Details

Journal
Chinese Journal of Chemistry
Published
2025-12-22
DOI
https://doi.org/10.1002/cjoc.70401
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Remote Construction of Diverse Heteropolycycles via 1,4‐Pd or 1,4/1,5‐Pd Migration‐Mediated Intermolecular Double C–H Annulation

Yun Teh S. Liang, Xingyue Pan, Peng Yu, Yuan Yang et al.
Chinese Journal of Chemistry
Catalytic C–H Functionalization Methods
article

Remote Construction of Diverse Heteropolycycles via 1,4‐Pd or 1,4/1,5‐Pd Migration‐Mediated Intermolecular Double C–H Annulation

Yun Teh S. Liang, Xingyue Pan, Peng Yu, Yuan Yang, Liwei Zhou, Kunkun Wang, Zhendong Cheng
article en

Abstract

Comprehensive Summary Although 1,4‐Pd migration has been widely used for the functionalization of remote C−H bonds, intermolecular double C−H annulation via this strategy remains elusive. Furthermore, catalytic reactions involving 1,5‐Pd migration are scarce due to competitive reductive elimination pathway. Herein, we report an intermolecular double C–H annulation of N ‐(2‐bromophenyl)‐2‐phenylacrylamides with 1, n ‐diynes mediated by 1,4‐Pd or sequential 1,4/1,5‐Pd migrations. The reaction proceeds through sequential Heck cyclization, alkyl‐to‐aryl 1,4‐Pd migration (or alkyl‐to‐aryl 1,4‐Pd migration followed by aryl‐to‐aryl 1,5‐Pd migration), dual alkyne insertion, and C–H activation, providing efficient access to both indolinone‐substituted tricyclic frameworks and tetracyclic indolinones. The method exhibits excellent regioselectivity, and preliminary mechanistic studies support the proposed pathway.

Chinese Journal of ChemistryVol. 44(6)
Changsha Medical University (CN), Hunan Normal University (CN), Anhui Normal University (CN), Hunan Agricultural University (CN)
National Natural Science Foundation of China
Reduced inequalities
Openalex Percentile: Top 34%
Catalytic C–H Functionalization Methods
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