ARTICLES

Reaction of Tandem Addition of Aliphatic Amines to Alkenylnitriles Catalyzed by Tris(o-dimethylaminobenzyl)yttrium

  • Jinsong Hou ,
  • Gaosheng Yang
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  • aMOE Key Laboratory of Functional Molecular Solids, Anhui Laboratory of Molecule-Based Materials, Institute of Organic Chemistry, College of Chemistry and Materials Science, Anhui Normal University, Wuhu, Anhui 241002
    bCollege of Material and Chemical Engineering, Chuzhou University, Chuzhou, Anhui 239000

Received date: 2022-03-01

  Revised date: 2022-04-05

  Online published: 2022-04-29

Supported by

National Natural Science Foundation of China(21672005); National Natural Science Foundation of China(20972001)

Abstract

Amidines are nitrogen-containing compounds with very important physiological activities. There are few reports on the synthesis of cyclic amidines catalyzed by rare earth complexes. In this paper, a series of cyclic amidines were synthesized by the tandem reaction of N—H to CN and “C=C” with simple trialkyl rare earth metal complex Y(CH2C6H4NMe2-o)3 as precatalyst with 22%~96% yields. The method has the characteristics of simple catalyst, mild reaction conditions and 100% atomic utilization. It provides a new way for the construction of cyclic amidines.

Cite this article

Jinsong Hou , Gaosheng Yang . Reaction of Tandem Addition of Aliphatic Amines to Alkenylnitriles Catalyzed by Tris(o-dimethylaminobenzyl)yttrium[J]. Chinese Journal of Organic Chemistry, 2022 , 42(7) : 2070 -2078 . DOI: 10.6023/cjoc202203002

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