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Cyanide-Free Ce(III)-Catalyzed Highly Efficient Synthesis of ?-Iminonitriles from 2-Aminopyridines and Nitroalkenes via Intermolecular Dehydration Reaction.


ABSTRACT: A direct and rapid method for the synthesis of ?-iminonitriles achieved good to excellent yields. A novel intermolecular dehydration reaction between 2-aminopyridines and nitroalkenes is reported via a rare-earth-metal catalyst. The merits of this transformation include cyanide-free protocol, short reaction time, simple operation, water as the only byproduct, commercially available reagents, good functional group tolerance, etc. Moreover, nitroalkenes are demonstrated as a new "CN" source in this transformation.

SUBMITTER: Chen Z 

PROVIDER: S-EPMC6644690 | biostudies-literature | 2018 Oct

REPOSITORIES: biostudies-literature

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Cyanide-Free Ce(III)-Catalyzed Highly Efficient Synthesis of α-Iminonitriles from 2-Aminopyridines and Nitroalkenes via Intermolecular Dehydration Reaction.

Chen Zhengwang Z   Liang Pei P   Zheng Jing J   Zhou Zhonggao Z   Wen Xiaowei X   Liu Tanggao T   Ye Min M  

ACS omega 20181003 10


A direct and rapid method for the synthesis of α-iminonitriles achieved good to excellent yields. A novel intermolecular dehydration reaction between 2-aminopyridines and nitroalkenes is reported via a rare-earth-metal catalyst. The merits of this transformation include cyanide-free protocol, short reaction time, simple operation, water as the only byproduct, commercially available reagents, good functional group tolerance, etc. Moreover, nitroalkenes are demonstrated as a new "CN" source in thi  ...[more]

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