“Cesium Effect”-Mediated/Controlled Divergent Synthesis via Synergistic Pd/Cu-Catalyzed Cascade Reactions

Herein, we describe a method in the one-pot synthesis of cyclic 1,3-enynes and allenynes from alkynyl-allenyl cross-coupling and cascade reactions of vinylidenecyclopropane-diesters (VDCP-diesters) with a large number of unactivated terminal alkynes for the formation of a C(sp2)–C(sp) bond under palladium/copper dual catalysis and assisted by base Cs2CO3 and NEt3 with distinctly different Brønsted basicity and Lewis basicity. This developed divergent transformation proceeds through a key rapid transmetalation and the subsequent intramolecular cyclization process regulated by cesium effect. Our investigations found that these reactions can occur under mild conditions and have a broad substrate scope with a wide range of functional groups via a zwitterionic palladium species, affording the corresponding desired products in moderate to good yields. Further synthetic transformations show the application value of this protocol. Plausible reaction mechanisms have also been proposed on the basis of control, deuterium labeling experiments, and density functional theory calculations.

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Publication Details

Journal
ACS Catalysis
Published
2025-05-05
DOI
https://doi.org/10.1021/acscatal.5c01895
Citations
2
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.87

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article

“Cesium Effect”-Mediated/Controlled Divergent Synthesis via Synergistic Pd/Cu-Catalyzed Cascade Reactions

Yong-Jie Long, Yin Wei, Xian-Hua Zhong, Min Shi
2 citations
ACS Catalysis
Catalytic C–H Functionalization Methods
1.87
article

“Cesium Effect”-Mediated/Controlled Divergent Synthesis via Synergistic Pd/Cu-Catalyzed Cascade Reactions

Yong-Jie Long, Yin Wei, Xian-Hua Zhong, Min Shi
article en
2 citations

Abstract

Herein, we describe a method in the one-pot synthesis of cyclic 1,3-enynes and allenynes from alkynyl-allenyl cross-coupling and cascade reactions of vinylidenecyclopropane-diesters (VDCP-diesters) with a large number of unactivated terminal alkynes for the formation of a C(sp2)–C(sp) bond under palladium/copper dual catalysis and assisted by base Cs2CO3 and NEt3 with distinctly different Brønsted basicity and Lewis basicity. This developed divergent transformation proceeds through a key rapid transmetalation and the subsequent intramolecular cyclization process regulated by cesium effect. Our investigations found that these reactions can occur under mild conditions and have a broad substrate scope with a wide range of functional groups via a zwitterionic palladium species, affording the corresponding desired products in moderate to good yields. Further synthetic transformations show the application value of this protocol. Plausible reaction mechanisms have also been proposed on the basis of control, deuterium labeling experiments, and density functional theory calculations.

ACS CatalysisVol. 15(10)
Shanghai Institute of Organic Chemistry (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China, Chinese Academy of Sciences, National Key Research and Development Program of China
Openalex Percentile: Top 16%
Catalytic C–H Functionalization Methods
1.87
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