Sign in
The regioselectivity of the 1,3-dipolar cycloaddition of alpha-carbonylformonitrile N-arylimides to benzylideneacetone and beta-diketones
Journal article

The regioselectivity of the 1,3-dipolar cycloaddition of alpha-carbonylformonitrile N-arylimides to benzylideneacetone and beta-diketones

Journal of chemical research. Synopses, (7), pp.316-317
01/07/1996

Abstract

Chemistry Chemistry, Multidisciplinary Physical Sciences Science & Technology
The cycloaddition of the ethoxycarbonylformonitrile N-arylimides 2 to benzylideneacetone afforded two regioisomers, 5-acetyl- and 4-acetyl-dihydropyrazoles, but the cycloaddition of 2 to benzoylacetone afforded 4-acetyl- and 4-benzoyl-pyrazole; some pyrazolopyridazin-7-one and pyrazolopyridazine derivatives were also synthesized.

Metrics

1 Record Views

Details