Heterocyclic Esters of 1,1'-Ferrocenedicarboxylic Acid
- Authors: Kolesnik I.A.1, Kletskov A.V.1, Petkevich S.K.1, Dikusar E.A.1, Potkin V.I.1
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Affiliations:
- Institute of Physical Organic Chemistry
- Issue: Vol 88, No 3 (2018)
- Pages: 462-469
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/222055
- DOI: https://doi.org/10.1134/S107036321803012X
- ID: 222055
Cite item
Abstract
Acylation of hydroxyl-containing heterocyclic compounds with 1,1'-ferrocenedicarbonyl chloride afforded diheteryl-1,1'-ferrocenedicarboxylates. Bisaldehyde-containing diesters were obtained by acylation of hydroxybenzaldehydes. The condensation of the latter with 2-naphthylamine or 4-phenylazoaniline resulted in the formation of the corresponding azomethines. The reduction of bisaldehyde-containing diesters furnished ferrocene-containing diols. Ferrocene tetrahydrobenzo[a]acridine-11-(7H)-one derivatives were synthesized as a result of the three-component cascade heterocyclization of ferrocene bisaldehyde-containing diesters with 2-naphthylamine and dimedone.
About the authors
I. A. Kolesnik
Institute of Physical Organic Chemistry
Email: dikusar@ifoch.bas-net.by
Belarus, ul. Surganova 13, Minsk, 220072
A. V. Kletskov
Institute of Physical Organic Chemistry
Email: dikusar@ifoch.bas-net.by
Belarus, ul. Surganova 13, Minsk, 220072
S. K. Petkevich
Institute of Physical Organic Chemistry
Email: dikusar@ifoch.bas-net.by
Belarus, ul. Surganova 13, Minsk, 220072
E. A. Dikusar
Institute of Physical Organic Chemistry
Author for correspondence.
Email: dikusar@ifoch.bas-net.by
Belarus, ul. Surganova 13, Minsk, 220072
V. I. Potkin
Institute of Physical Organic Chemistry
Email: dikusar@ifoch.bas-net.by
Belarus, ul. Surganova 13, Minsk, 220072