Novel bipodal, tripodal, and tetrapodal 1,4-dihydropyridines - Microwave-assisted synthesis and structural confinements

被引:12
作者
Rajesh, Kancherla [1 ]
Reddy, Bandapalli Palakshi [1 ]
Vijayakumar, Vijayaparthasarathi [1 ]
机构
[1] VIT Univ, Sch Adv Sci, Div Organ Chem, Synthet Organ Chem Res Lab, Vellore 632014, Tamil Nadu, India
来源
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE | 2011年 / 89卷 / 10期
关键词
bipodal-tripodal-tetrapodal 1,4-dihydropyridines; Hantzsch pyridines; microwave irradiation; DERIVATIVES;
D O I
10.1139/V11-088
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The one pot, three component reaction of p-hydroxy benzaldehyde, beta-ketoester, and ammonium acetate afforded the corresponding monopodal 1,4-dihydropyridines as building blocks, which in turn converted into diversified novel bipodal, tripodal, and tetrapodal 1,4-dihydropyridines with different alkylating agents through conventional as well as microwave assisted reactions. The unambiguous structural confinements of the all the synthesized compounds were drawn out with the help of 2D NMR (H-H COSY and C-H COSY).
引用
收藏
页码:1236 / 1244
页数:9
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