Heterocyclic Esters of 1,1'-Ferrocenedicarboxylic Acid View Full Text


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Article Info

DATE

2018-03

AUTHORS

I. A. Kolesnik, A. V. Kletskov, S. K. Petkevich, E. A. Dikusar, V. I. Potkin

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. More... »

PAGES

462-469

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s107036321803012x

DOI

http://dx.doi.org/10.1134/s107036321803012x

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1103400086


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