New functionalized pyrazolines from 1-aroyl-2-phenylacetylenes and thiocarbonohydrazides View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2006-11

AUTHORS

M. Yu. Dvorko, A. I. Albanov, N. N. Chipanina, L. V. Sherstyannikova, V. G. Samoilov, T. N. Komarova, T. E. Glotova

ABSTRACT

The reaction of 1-aroyl-2-phenylacetylenes with thiocarbonohydrazide and benzaldehyde thiocarbohydrazone in acetic acid-water or ethanol-water systems with the reagents in an equimolar ratio leads to the selective formation of 1-carbothiohydrazinoyl-5-hydroxy-3-phenyl-5-R-2-pyrazolines. Ring-chain tautomerism involving the enamine and hydrazone forms was detected for solutions of the pyrazolines (with R = 2-thienyl) in DMSO.

PAGES

1421-1426

References to SciGraph publications

  • 2002-08. Thiocarbohydrazide as ``Diamine'' to Construct Macrocyclic and Side-Off Compartmental Ligands in JOURNAL OF INCLUSION PHENOMENA AND MACROCYCLIC CHEMISTRY
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1007/s10593-006-0258-0

    DOI

    http://dx.doi.org/10.1007/s10593-006-0258-0

    DIMENSIONS

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