85336-18-1Relevant academic research and scientific papers
Oxidative dearomatization of phenols and anilines via λ3 - and λ5-iodane-mediated phenylation and oxygenation
Quideau, Stephane,Pouysegu, Laurent,Ozanne, Aurelie,Gagnepain, Julien
, p. 201 - 216 (2005)
Treatment of 2-methylphenols with chloro(diphenyl)-λ3- iodane led to their regioselective dearomatizing 2-phenylation into cyclohexa-2,4-dienone derivatives via a proposed ligand coupling reaction. In the same vein of investigation, treatment of 2-methylanilines with the λ5-iodane 2-iodoxybenzoic acid IBX reagent led to their regioselective dearomatization into previously undescribed ortho-quinol imines.
NOVEL COMPOUND AND ORGANIC ELECTROLUMINESCENCE DEVICE
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Paragraph 0412; 0413, (2020/12/13)
A compound represented by the following formula (1):
Metal complexes of tetra(6-tert-butyl-2,3-quinolino)porphyrazine: I. Synthesis
Efimova,Korzhenevskii,Koifman
scheme or table, p. 1614 - 1621 (2009/06/28)
Complexes of tetra(6-tert-butyl-2,3-quinolino)porphyrazine with Cu, Co, Zn, and Ni soluble in hydrophobic liquids were synthesized for the first time by template tetramerization of derivatives of 6-tert-butylquinoline-2,3- dicarboxylic acid formed from the corresponding acid in the course of carbamide synthesis in presence of the bivalent metal ions.
