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Updated: Oct 15, 2025

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Selective divergent radical cyclization of 1,6-dienes with alkyl nitriles
Qing-Qing Kang1, Yi Liu1, Shi-Ping Wu1
1Key Laboratory of Advanced Mass Spectrometry and Molecular Analysis of Zhejiang Province, State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products, School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang, 315211, China. weiwenting@nbu.edu.cn.
Abstract:
An efficient, selective, and step economical radical cyclization of 1,6-dienes with alkyl nitriles initiated by α-C(sp3)-H functionalization under the Sc(OTf)3 and Ag2CO3 system is described here. The selective divergent cyclization relies on the substitution effect at the α-position of the acrylamide moiety and nitriles, which is terminated by hydrogen abstraction, direct cyclization with the aryl ring, or further cyclization with the CN bond and hydrolysis, respectively.
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