M 39 Matern, A. I. Progress in the studies of oxidation of dihydropyridines and their analogues [Electronic resource] / A. I. Matern, V. N. Charushin, O. N. Chupakhin // Russian Chemical Reviews. - 2007. - Vol. 76, № 1. - P23-40 Рубрики: ХИМИЧЕСКИЕ НАУКИ Аннотация: Published data on oxidation of dihydropyridines and on the mechanisms and the role of hydride shifts in bioorganic chemistry, enantioselective synthesis and supramolecular chemistry are generalised. \\\\Expert2\\nbo\\Russian Chemical Reviews\\2007, V.76, N1, p.23.pdf |
I-70 Investigation of nanosized metal oxides as stereoselective catalysts of the Hantzsch and Biginelli reactions [Text] / O. V. Fedorova, I. G. Ovchinnikova, V. G. Kharchuk, G. L. Rusinov, M. A. Uimin, A. A. Mysik, A. Ye. Yermakov, Y. R. Uhm, C. K. Rhee, V. N. Charushin // 8-th International Symposium on Nanocomposites and Nanoporous Materials (ISNNM8) , Jeju, Korea, Febr. 22-24. 2007. - Jeju Haevichi Resort, Korea, 2007. - P181-182 Рубрики: ХИМИЧЕСКИЕ НАУКИ |
I-70 Investigation of nanosized metal oxides as stereoselective catalysts of the Hantzsch and Biginelli reactions [Text] / O. V. Fedorova, I. G. Ovchinnikova, V. G. Kharchuk, G. L. Rusinov, M. A. Uimin, A. A. Mysik, A. Ye. Yermakov, Y. R. Uhm, C. K. Rhee, V. N. Charushin // 1-th Korean-Russian Joint Seminar for the Functional Nano Materials, Jeju, Korea, Febr. 22-24 2007 . - Jeju, Haevichi Resort, Korea, 2007 Рубрики: ХИМИЧЕСКИЕ НАУКИ |
R 30 Reactions of pyrazinium salts with phenols:from σH-adducts to SN Hproducts and transformations into benzo[b]furans / E. V. Verbitskiy, Yu. A. Kvashnin, P. A. Slepukhin, A. V. Kuchin, G. L. Rusinov, O. N. Chupakhin, V. N. Charushina // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2011. - Vol.60, №5. - С. 919-928 Рубрики: ХИМИЧЕСКИЕ НАУКИ Кл.слова (ненормированные): DIHYDROPYRIDINES -- NUCLEOPHILIC SUBSTITUTION -- HYDROGEN Аннотация: The reaction of 5-(het)aryl-2,3-dicyano-1-ethylpyrazinium salts with phenol derivatives affords relatively stable dihydropyrazines, whereas the reactions of 6-(het)aryl-1,2,5-oxadiazolo[3,4-b]pyrazin-4-ium protic salts, depending on the phenol structure, result in products of nucleophilic substitution of hydrogen or open-chain transformation products: benzo[b]furan-substituted derivatives. The crystallographic data on the spatial structure of all types of the synthesized products were obtained \\\\Expert2\\nbo\\Russian Chemical Bulletin\\2011, 60 (5), 919-928.pdf |