Journal of Heterocyclic Chemistry · 1982 · 13 citations · 5 references
Natural SciencesChemistryMedicinal ChemistryCatalysisOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsOrganic SynthesisSubstitution ReactionsBase CatalysisMild Reaction ConditionsNucleophilic ReactivityNucleophilic Substitution In Heterocycles
Abstract The trichloromethyl group served as a useful leaving group in nucleophilic displacement reactions by a variety of substituted amines and alcohols (the latter under base catalysis) on 2‐trichloromethyl‐5‐methyl‐1,3,4,6,9b‐pentaazaphenalene ( 1a ) and 2‐trichloromethyl‐4‐cyano‐1,3,6,9b‐tetraazaphenalene ( 2a ). The reaction conditions were mild and the yields of the corresponding 2‐substituted amino and alkoxy derivatives were generally good.
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A.R. Katritzky · Nature Physical Science · 1973 · 68 citations · Full text
The Synthesis of 1,3,6-Triazacycl[3.3.3]azines.
Olof Ceder, Johanna E. Andersson, Leif J. Sæthre et al. · Acta chemica Scandinavica/Acta chemica Scandinavica. B, Organic chemistry and biochemistry/Acta chemica Scandinavica. A, Physical and inorganic chemistry/Acta chemica Scandinavica. Series B. Organic chemistry and biochemistry/Acta chemica Scandinavica. Series A, Physical and inorganic chemistry · 1972 · 19 citations · Full text