Aroyl[bis(4-hydroxycoumarin-3-yl)]methanes in reactions with 1,2-diaminobenzenes |
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Authors: | N. N. Kolos L. L. Gozalishvili F. G. Yaremenko O. V. Shishkin S. V. Shishkina I. S. Konovalova |
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Affiliation: | (1) V. N. Karazin Kharkov National University, 4 pl. Svobody, 61077 Kharkov, Ukraine;(2) V. Ya. Danilevsky Institute of Endocrine Pathology Problems, Academy of Medical Sciences of Ukraine, 10 ul. Artema, 61077 Kharkov, Ukraine;(3) State Scientific Institution “Institute for Single Crystals”, National Academy of Sciences of Ukraine, 40 prosp. Lenina, 61002 Kharkov, Ukraine |
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Abstract: | The reaction of aroyl[bis(4-hydroxycoumarin-3-yl)]methanes with 1,2-phenylenediamines in PriOH is accompanied by the recyclization to 8-R-or 7-R-4-(2-hydroxyphenyl)-1,5-benzodiazepin-2-ones, whereas the reaction with o-phenylenediamine and its 4-methyl-substituted derivatives in MeOH produces organic ionic salts of the bis-coumarin anion with monoprotonated o-phenylenediamine as the cation. Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2200–2205, November, 2007. |
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Keywords: | aroyl[bis(4-hydroxycoumarin-3-yl)]methanes 4-R-1,2-diaminobenzenes 8-R-(7-R)-4-(2-hydroxyphenyl)-1,5-benzodiazepin-2-ones recyclization ionic salts X-ray diffraction study |
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