JOURNAL 689


Organic Communications
VOLUME & ISSUE
Year: 2014 Issue: 4 October-December
PAGES
p.137 - 143
STATISTICS
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AUTHORS
    Hany M. Dalloul
PDF OF ARTICLE

GRAPHICAL ABSTRACT


ABSTRACT


A number of new substituted 1,2,4,9,10,12-hexaazadispiro[4.2.4.2]tetra-deca-2,10-dienes have been obtained from the reaction of 1,4-cyclohexanedione hydrazones having acetyl, benzoyl, ethoxycarbonyl and methoxycarbonyl groups with appropriate nitrilimines. The microanalysis and spectral data of the synthesized compounds are in full agreement with their molecular structure. The microbial features of the synthesized compounds were studied by a known method.

KEYWORDS
  • Dispiroheterocycles
  • 1
  • 4-cyclohexanedione hydrazones
  • nitrilimines
  • 1
  • 3-dipolar cycloaddition