A rapid and efficient domino protocol for the synthesis of functionalized benzo[a]pyrano[2,3-c]phenazine and benzo[f]pyrano[2,3-h]quinoxaline derivatives

被引：22

作者：

Mohebat, Razieh ^{[1
]}

Abadi, Afshin Yazdani Elah ^{[2
]}

Maghsoodlou, Malek-Taher ^{[2
]}

机构：

[1] Islamic Azad Univ, Dept Chem, Yazd Branch, POB 89195-155, Yazd, Iran

[2] Univ Sistan & Baluchistan, Dept Chem, Fac Sci, Zahedan, Iran

来源：

RESEARCH ON CHEMICAL INTERMEDIATES | 2016年 / 42卷 / 06期

关键词：

Multi-component domino reactions (MDRs); Tetracyanoethylene; Pyridine; Benzo[a] pyrano[2,3-c] phenazine; Benzo[f]pyrano[2,3-h]quinoxaline; ONE-POT SYNTHESIS; QUINOXALINE DERIVATIVES; NATURAL-PRODUCTS; AGENTS; HETEROCYCLES; ALKALOIDS; FACILE;

D O I：

10.1007/s11164-016-2437-7

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Benzo[a]pyrano[2,3-c]phenazine and benzo[f]pyrano[2,3-h]quinoxaline derivatives were synthesized via a one-pot, two-step procedure from a three-component condensation reaction of 2-hydroxynaphthalene-1,4-dione, 1,2-diamines, and tetracyanoethylene in the presence of pyridine as an efficient catalyst. This novel procedure has the advantages of operational simplicity, short reaction times, easy work-up, avoiding costly syntheses, and the products do not require further purification, which provides an efficient and economical method for the synthesis of related products in excellent yields.

引用

页码：6039 / 6048

页数：10

共 45 条

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