SYNTHESIS OF FORMYL DERIVATIVES OF 2-HETARYLIMIDAZOLES ANNELATED WITH NAPHTHALENE AND PHENANTHRENE RINGS

Authors

  • А. А. Печкин Scientific-Research Institute of Physical and Organic Chemistry, Rostov State University, Rostov-on-Don
  • М. М. Ельчанинов Southern Russia State Technical University (Novocherkassk Polytechnic Institute), Novocherkassk 346400
  • Б. С. Лукьянов Scientific-Research Institute of Physical and Organic Chemistry, Rostov State University, Rostov-on-Don
  • Ю. С. Алексеенко Scientific-Research Institute of Physical and Organic Chemistry, Rostov State University, Rostov-on-Don

Keywords:

hetarylimidazoles, formylation

Abstract

The formylation reaction of a series of 2-hetarylimidazoles, annelated by naphthalene and phenanthrene rings, using hexamethylenetetramine in PPA and the Vilsmeier reagent has been studied. The furyl and thienyl derivatives form principally the 5-formyl-substituted and the pyrrolylimidazoles were found to give a mixture of the α- and β-formyl derivatives.

How to Cite
Pechkin, A. A.; Elchaninov, M. M.; Lukyanov, B. S.; Alekseenko, Yu. S. Chem. Heterocycl. Compd. 2004, 40, 599. [Khim. Geterotsikl. Soedin. 2004, 711.]

For this article in the English edition, see DOI 10.1023/B:COHC.0000037315.48485.a2

Downloads

Published

2004-05-25

Issue

No. 5 (2004)

Section

Original Papers