Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Dmitry S. Fadeev"'
Publikováno v:
Pedagogy and Psychology of Education. :109-125
Publikováno v:
Journal of Inclusion Phenomena and Macrocyclic Chemistry. 96:245-250
The design and the preparation of a small library of optically active polyazamacrocyclic compounds with a furan bridge, connected by (4-(methylaminomethyl)-1,2,3-triazole) rings with methylene, ethyloxyethyl or ethylethoxyethyl units from natural lab
Autor:
Dmitry S. Fadeev, Nariman F. Salakhutdinov, Yuriy V. Gatilov, Yana L Esaulkova, Vladimir V. Chernyshov, Olga I. Yarovaya, Katherina O Sinegubova, Anna S Muryleva, Vladimir V. Zarubaev
Publikováno v:
Molecular Diversity
An effective technique for one-stage synthesis of new polycyclic nitrogen-containing compounds has been developed. The procedure involves refluxing mixtures of camphoric acid with aliphatic or aromatic diamine without catalysts. In cases where the st
Publikováno v:
Journal of Fluorine Chemistry. 210:88-93
1,1-Difluoronaphthalen-2(1H)-ones were used as building blocks for synthesis of functionalized fluorinated tetraphenones via Diels-Alder reaction. Two effective methods of tetraphenone reductive aromatization were proposed. Fully aromatic stable fluo
Autor:
Denis S. Baranov, P. A. Kuchinskaya, Dmitriy E. Utkin, Danil A. Nevostruev, Mikhail N. Uvarov, Evgeni M. Glebov, Leonid V. Kulik, Olga V. Antonova, S. A. Gromilov, Evgeny A. Mostovich, Maxim S. Kazantsev, A. S. Sukhikh, Dmitry S. Fadeev
Publikováno v:
Dyes and Pigments. 150:252-260
Annulation of the two pyrimidine rings with anthraquinone through the simple condensation of the 1,5-diiodoanthraquinone with guanidine was employed to build 1,3,7,9-tetraazaperylene framework functionalized by NH2, C=O, aliphatic and alkoxy-groups.
Publikováno v:
Journal of Fluorine Chemistry. 199:20-29
1,1-Difluoronaphthalene-2(1H)-ones were proposed as novel fluorinated dienophiles for the Diels-Alder reaction. The influence of the diene structure, reaction conditions on the rate and diastereoselectivity of the Diels-Alder cycloaddition was studie
Autor:
Anastasiya I. Govdi, Valentine G. Nenajdenko, Sergey F. Vasilevsky, Victor I. Mamatyuk, Dmitry S. Baev, Nadezda V. Sokolova, Irina V. Sorokina, Dmitry S. Fadeev, Tatyana G. Tolstikova
Publikováno v:
MedChemComm. 6:230-238
The modification of betulinic acid derivatives bearing an ethynyl group at the C-3 position by different azidopeptides using Cu(I)-catalyzed alkyne-azide cycloaddition has been described. All obtained compounds were tested for their anti-inflammatory
Autor:
Sergey F. Vasilevsky, V. I. Mamatyuk, Dmitry S. Fadeev, I. V. Sorokina, T. G. Tolstikova, Maria P. Davydova
Publikováno v:
Russian Journal of Bioorganic Chemistry. 41:70-76
A new approach to the synthesis of natural combretastatin A-4 analogues based on the interaction of α-acetylenic ketones with secondary amines (diethyl amine, pyrrolidine, piperidine, morpholine) was proposed. Previously unknown analogues of combret
Autor:
Denis S. Baranov, Dmitry S. Fadeev
Publikováno v:
Mendeleev Communications. 26:174-176
New 2-octyloxy-7H-benzo[e]perimidin-7-one and 3-benzylor 3-propargyl-3H-benzo[e]perimidine-2,7-diones were synthesized from 1-iodoanthraquinone. The propargyl derivative was subjected to Mannich and cycloaddition reactions.
Autor:
Dmitry S. Fadeev, S. F. Vasilevskii, T. F. Mikhailovskaya, V. I. Mamatyuk, Aleksandr A. Stepanov
Publikováno v:
Russian Journal of Organic Chemistry. 50:506-509
Sonogashira alkynylation of methyl 2-iodobenzoate with terminal acetylenes gave a series of methyl 2-(alk-1-yn-1-yl)benzoates which reacted with hydroxylamine in boiling methanol to produce five- or six-membered N-hydroxy lactams, 3-R-methylidene-2-h