SYNTHESIS OF 3-ARYLCOUMARINS BY A FeCl<sub>3</sub>-PROMOTED CYCLIZATION OF <i>ortho</i>-METHOXY SUBSTITUTED (<i>E</i>)-2,3-DIPHENYLPROPENOIC ACIDS OR THEIR METHYL ESTERS

Authors

  • H. Y. Ge School of Chemical Engineering, Huaihai Institute of Technology, Lianyungang 222005, P. R. China
  • Z. J. Fang School of Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, P. R. China
  • B. H. Qian School of Chemical Engineering, Huaihai Institute of Technology, Lianyungang 222005, P. R. China

DOI:

https://doi.org/10.1007/1201

Keywords:

3-arylcoumarin, iron(III) chloride, synthesis, tandem reaction

Abstract

3-Arylcoumarins were conveniently synthesized in excellent yields by an iron(III) chloride-promoted tandem reaction using methoxy-substituted (E)-2,3-diphenylpropenoic acids or their methyl esters. The structure of 3-(4-methoxyphenyl)coumarin was established
from X-ray crystallographic data.

How to Cite
Ge, H. Y.; Fang, Z. J.; Qian, B. H. Chem. Heterocycl. Compd. 2014, 50, 12. [Khim. Geterotsikl. Soedin. 2014, 17.]

For this article in the English edition see DOI 10.1007/s10593-014-1442-2

Author Biographies

H. Y. Ge, School of Chemical Engineering, Huaihai Institute of Technology, Lianyungang 222005, P. R. China

Hong-Yu Ge

Z. J. Fang, School of Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, P. R. China

Zhi-Jie Fang

B. H. Qian, School of Chemical Engineering, Huaihai Institute of Technology, Lianyungang 222005, P. R. China

Bao-Hua Qian

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Published

2014-02-05

Issue

No. 1 (2014)

Section

Original Papers