Efficient one-pot synthesis of novel and diverse tetrahydroquinolines bearing pyranopyrazoles using organocatalyzed domino Knoevenagel/hetero Diels-Alder reactions

被引:17
|
作者
Pandit, Rameshwar Prasad [1 ]
Lee, Yong Rok [1 ]
机构
[1] Yeungnam Univ, Sch Chem Engn, Kyongsan 712749, South Korea
基金
新加坡国家研究基金会;
关键词
Tetrahydroquinolines; Pyrazolones; Aminoaldehydes; Knoevenagel condensation; Hetero Diels-Alder reaction; INTRAMOLECULAR CYCLIZATION; FACILE SYNTHESIS; INHIBITORS; DERIVATIVES; PROTEIN; VIRANTMYCIN; DISCOVERY; QUINOLINE; STRAIN; PYRANO;
D O I
10.1007/s11030-013-9482-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A new synthetic route to biologically interesting diverse tetrahydroquinolines bearing pyranopyrazoles was developed by reacting pyrazolones and ,-dialkylated aminobenzaldehydes in the presence of EDDA. The key strategy underlying the methodology used was the domino Knoevenagel/hetero Diels-Alder reaction. This synthetic method provides a variety of novel tetrahydroquinolines in good yields.
引用
收藏
页码:39 / 50
页数:12
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