Tetrahedron

Novel solid-supported dimerization–heteroannulation of chalcones: simple and efficient synthesis of 2, 4, 6-triaryl-3-methylarylpyridines

AK Verma, S Koul, APS Pannu, TK Razdan

Index: Verma, Anil K.; Koul, Summon; Pannu, Ajay P.S.; Razdan, Tej K. Tetrahedron, 2007 , vol. 63, # 36 p. 8715 - 8722

Full Text: HTML

Citation Number: 16

Abstract

2, 4, 6-Triaryl-3-methylarylpyridines were obtained, in 60–70% yield, by a novel one-pot solventless solid-supported dimerization–heteroannulation reaction of chalcones and compounds possessing terminal–CONH2 functionality, at 125–135° C, using immobilized Bi (III) nitrate and Zn (II) chloride as co-catalyst. Initially, chalcones were prepared, in nearly quantitative yield, by a modified aldol condensation, in neutral aqueous medium, in the ...

Related Articles:

Synthesis and anti-inflammatory, analgesic, ulcerogenic and lipid peroxidation activities of 3, 5-dimethyl pyrazoles, 3-methyl pyrazol-5-ones and 3, 5-disubstituted …

[Amir, Mohd; Kumar, Shikha Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2005 , vol. 44, # 12 p. 2532 - 2537]

Design, synthesis and SAR study of hydroxychalcone inhibitors of human β-secretase (BACE1)

[Ma, Lei; Yang, Zhengyi; Li, Chenjing; Zhu, Zhiyuan; Shen, Xu; Hu, Lihong Journal of Enzyme Inhibition and Medicinal Chemistry, 2011 , vol. 26, # 5 p. 643 - 648]

Hydration of the flavylium ion

[Journal of the American Chemical Society, , vol. 102, # 18 p. 5838 - 5848]

Design, synthesis and SAR study of hydroxychalcone inhibitors of human β-secretase (BACE1)

[Journal of Enzyme Inhibition and Medicinal Chemistry, , vol. 26, # 5 p. 643 - 648]

Design, synthesis and SAR study of hydroxychalcone inhibitors of human β-secretase (BACE1)

[Journal of Enzyme Inhibition and Medicinal Chemistry, , vol. 26, # 5 p. 643 - 648]

More Articles...