Synthesis 2025; 57(07): 1306-1312
DOI: 10.1055/a-2508-3790
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Nickel(II)-Catalyzed Cycloisomerization of 1,6-Dienes

Zhongjian Du
a   School of Chemistry and Chemical Engineering, Hefei University of Technology and Anhui Province Key Laboratory of Value-Added Catalytic Conversion and Reaction Engineering, Hefei 230009, P. R. of China
,
Chenlei Ji
a   School of Chemistry and Chemical Engineering, Hefei University of Technology and Anhui Province Key Laboratory of Value-Added Catalytic Conversion and Reaction Engineering, Hefei 230009, P. R. of China
,
Xu Wang
a   School of Chemistry and Chemical Engineering, Hefei University of Technology and Anhui Province Key Laboratory of Value-Added Catalytic Conversion and Reaction Engineering, Hefei 230009, P. R. of China
,
Sijian Zhang
a   School of Chemistry and Chemical Engineering, Hefei University of Technology and Anhui Province Key Laboratory of Value-Added Catalytic Conversion and Reaction Engineering, Hefei 230009, P. R. of China
,
Zhenyu Wang
b   Anhui Province Key Lab of Green Manufacturing in Phosegene Industry, Caijiashan Fine Chem Pk, Xinhang 242235, P. R. of China
,
a   School of Chemistry and Chemical Engineering, Hefei University of Technology and Anhui Province Key Laboratory of Value-Added Catalytic Conversion and Reaction Engineering, Hefei 230009, P. R. of China
› Institutsangaben
This work was supported by the National Natural Science Foundation of China (22401070), Anhui Postdoctoral Science Foundation (2023B666), and the Fundamental Research Funds for the Central Universities of China (PA2024GDSK0102).


Abstract

A nickel-catalyzed protocol for the cycloisomerization of 1,6-dienes has been developed. Using commercially available NiBr₂ and PPh₃ as catalysts, Zn as a reductant, and ZnI₂ as an additive, the methodology efficiently converts various 1,6-dienes into pyrrolidine derivatives in excellent yields and high selectivity.

Supporting Information



Publikationsverlauf

Eingereicht: 02. Dezember 2024

Angenommen nach Revision: 26. Dezember 2024

Accepted Manuscript online:
03. Januar 2025

Artikel online veröffentlicht:
20. Februar 2025

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