Synthesis of Pyrimidines with Ammonium Acetate as Nitrogen Source Under Solvent‐Free Conditions | Zendy

Wang Peigen | Zendy; Zhang Xueguo | Zendy; Liu Yafeng | Zendy; Chen Baohua | Zendy

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Synthesis of Pyrimidines with Ammonium Acetate as Nitrogen Source Under Solvent‐Free Conditions

Author(s) -

Wang Peigen,

Zhang Xueguo,

Liu Yafeng,

Chen Baohua

Publication year - 2019

Publication title -

asian journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.846

H-Index - 44

eISSN - 2193-5815

pISSN - 2193-5807

DOI - 10.1002/ajoc.201900248

Subject(s) - chemistry , ammonium acetate , chalcone , nitrogen , solvent , ammonium , tandem , ring (chemistry) , alcohol , organic chemistry , benzyl alcohol , catalysis , materials science , high performance liquid chromatography , composite material

A three‐component tandem reaction for the synthesis of multisubstituted pyrimidines from chalcone, benzyl alcohol and NH 4 OAc have been developed. This transformation represents an example for the simultaneous formation of two new C(sp 2 )−N bonds and a six‐membered ring using NH 4 OAc as nitrogen source under solvent‐free conditions.

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