Journal of Heterocyclic Chemistry · 1979 · 21 citations · 4 references
Natural SciencesChemistryMedicinal ChemistryGreen ChemistryOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisSubstitution Reactions1, 3-Dipolar CycloadditionRing-forming Reactions
Abstract The dipolar 1,4‐cycloaddition of dichloroketene to N,N ‐disubstituted 3‐amino‐1‐phenyl‐2‐propene‐1‐onesled directly to N,N ‐disubstituted 4‐amino‐3‐chloro‐6‐phenyl‐2 H ‐pyran‐2‐ones only in the case of an usual aliphatic N,N ‐disubstitution. In the case of partial or full aromatic N ‐substitution, N,N ‐disubstituted 4‐amino‐3,3‐dichloro‐3,4‐dihydro‐6‐phenyl‐2 H ‐pyran‐2‐ones were instead obtained, which were dehydrochlorinated with DBN to the corresponding 4‐amino‐3‐chloro‐6‐phenyl‐2 H ‐pyran‐2‐ones.
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Gaetano Bignardi, F. Fvangelisti, P. SCHENONE et al. · Journal of Heterocyclic Chemistry · 1972 · 27 citations
Luisa Mosli, Giulia Menozzi, P. SCHENONE · Journal of Heterocyclic Chemistry · 1978 · 22 citations