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A New Synthetic Pathway to Triphenylpyridines via Cascade Reactions Utilizing a New Iron‐Organic Framework as a Recyclable Heterogeneous Catalyst
Author(s) -
Doan Son H.,
Tran Nhu K. Q.,
Pham Phuc H.,
Nguyen Vu H. H.,
Nguyen Ngoc N.,
Ha Phuong T. M.,
Li Shuang,
Le Ha V.,
Le Nhan T. H.,
Tu Thach N.,
Phan Nam T. S.
Publication year - 2019
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201900094
Subject(s) - chemistry , catalysis , cascade , heterogeneous catalysis , ammonium acetate , organic synthesis , homogeneous , homogeneous catalysis , organic reaction , metal organic framework , organic chemistry , combinatorial chemistry , chemical engineering , chromatography , physics , high performance liquid chromatography , engineering , thermodynamics , adsorption
A new iron‐organic framework, VNU‐22 {[Fe 3 (BTC)(BPDC) 2 ] · 11.97H 2 O}, constructed from BTC 3– , BPDC 2– pillars and infinite [Fe 3 (CO 2 ) 7 ] ∞ rod SBU, was obtained. The VNU‐22 was utilized as a heterogeneous catalyst in the synthesis of 2,4,6‐triphenylpyridines via cascade reactions from acetophenones and phenylacetic acids with ammonium acetate as a nitrogen source. This transformation is new. The VNU‐22 was more active in the cascade reactions than many homogeneous and heterogeneous catalysts. The framework catalyst was recovered and reutilized without an appreciable decline in its performance. To our best knowledge, this synthetic pathway to 2,4,6‐triphenylpyridines was not previously reported, and would attract interests from the chemical industry.