INTERACTION OF 3-SUBSTITUTED INDOLES WITH PHENYLGLYOXAL

Authors

  • С. П. Ивонин Dnepropetrovsk National University, Dnepropetrovsk 49050
  • А. В. Лапандин Dnepropetrovsk National University, Dnepropetrovsk 49050

DOI:

https://doi.org/10.1007/8139

Keywords:

arylhydroxals, hydrazones, indoles, electrophilic substitution

Abstract

The interaction of 3-substituted indoles with phenylglyoxal has been studied. It was shown that a methyl group directs attack to the nitrogen atom, but hydrazonomethyl to position 2 of the indole. The reasons for the difference in regioselectivity are discussed.

How to Cite
Ivonin, S. P.; Lapandin, A. V.  Chem. Heterocycl. Compd. 2005, 41, 1390. [Khim. Geterotsikl. Soedin. 2005, 1653.]

For this article in the English edition, see DOI 10.1007/s10593-006-0007-4

 

Downloads

Published

2023-10-16

Issue

No. 11 (2005)

Section

Original Papers