Khim. D. Nicodemus, German Patent No. This leaves one unhybridized p orbital on each ring atom, which is perpendicular to the plane of the ring and parallel to other p orbitals. Otd. Zh. N. A. Titova, G. N. Abaev, V. V. Vetrova, B. F. Ustavshchikov, and G. K. Denisova, Zh. UDC 542.91:547.869:547.85, The aim of the proposed project is to create a new generation of potential molecular switches based on C60 and C70 fullerenes to be functionalized, as well as to develop effective synthetic methods, Recently, in the laboratory of catalytic synthesis of the Institute of Petrochemistry and Catalysis of RAS (head corr.-member of RAS U.M.Dzhemilev) developed new reaction, which has no analogues in, Enhancement of the anticancer therapy efficiency is the most important social and medical problem in the Russian Federation and all over the world. S. Sano, G. Koga, and S. Adzima, Japanese Patent No. A. Abdurakhmanov, Author's Abstract of Thesis for Candidate of Chemical Sciences [in Russian], Tashkent (1974). Commun., No. AlCl3–n Hamihama and I. Khayasi, Japanese Patent No. As part of the proposed project with the above reaction, it is planned to develop common approaches to the stereoselective production of natural and synthetic lembehynes (lembehyn A, B, C), the study of their neuritogenic and cytotoxic properties on cell lines, as well as the study of patterns of structure activity. Ser. Chem.,107, 145 (1924). Izobr., No. Khim., No. Khim., 40881 (1956). Soc. Zap, Yaroslavskogo Tekhnologicheskogo Instituta,22, 42 (1973). Formation of benzene derivatives, Lambert Brandsma, Preparative Acetylenic Chemistry, RSF: Synthesis and electronic properties of functionalized fullerenes as nanosized optical molecular switches, RSF: Design, synthesis and study of neuritogenic activity of lembehynes and their derivatives as innovative drugs for the treatment of neurodegenerative diseases, RSF: New generation of target anticancer drugs based on natural and synthetic 5Z,9Z-dienic acids: development and study of the molecular mechanisms, Mechanisms of Homogeneous Catalytic Reactions. W. Holdrich, N. Goetz, and G. Fouquet, German Patent No. Khim. Nauk SSSR. R. S. Sagitullin, Khim. Read "ChemInform Abstract: Synthesis of Complex Pyridine Bases by the Reaction of v‐Cyano‐α‐acetylenes with Acetylene Catalyzed by Cobalt Complexes., ChemInform" on DeepDyve, the largest online rental service for scholarly research with thousands of academic publications available at … Vereshchagin and I. L. Kotlyarevskii, Inventor's Certificate No. 21,536; Ref. The reactions afford cyclic and acyclic organoaluminum compounds. 1,240,928; Ref. Am. Obshch.,54, 420 (1924). Actually, the process is a modification of Reppe synthesis. Zh. All rights reserved. Khim. Khim., 5N166P (1974). All content in this area was uploaded by Usein M Dzhemilev. 1,069,368; Ref. 117,787; Byull. 179; Ref. 1, 65 (1977). Jpn.,72, 607 (1952); Chem. Khim., 13N135P (1964). Akad. Abs.,38, 2040 (1944). Ts. synthesis. To subscribe to email alerts, please log in first, or sign up for a DeepDyve account if you don’t already have one. 9, 2042 (1987). (4b) was oxidatively converted into N,N′-vinylene linked bisporphyrin free base. E. Dürkopf and H. Göttsch, Berichte,23, 685 (1890). Considering the above, the detailed investigation into molecular mechanisms of topoisomerase inhibitor effective action is of particular interest in terms of optimizing traditional schemes of drug therapy. C. E. Becker, U. S. Patent No. Khim. France, No. K. R. Hargrave, British Patent No. Reset filters. D. S. Petrenko, G. P. Geid, and V. A. Leites, Koks i Khimiya, No. discover and read the research Review [in Russian], Moscow (1978). Khim., 1N234P (1967). Khim., 68716P (1959). Akad. i Khim. 1,208,569, Ref. and Eng. 920,526; Ref. Khim. Jpn.,72, 711 (1952). A. D. Kagarlitskii, B. V. Suvorov, and S. R. Rafikov, Zh. J. Falz, J. E. Mahan, and D. White, Petrol. S. M. Tirabdzhanov, D. Yusupov, and A. M. Wiess, J. Khim., 18N99P (1972). DZHEMILEV, DZHEMILEV; SELIMOV, SELIMOV; KHAFIZOV, KHAFIZOV. J. E. Mahan, U. S. Patent No. 504,238; Chem. Russk. Khim., 24N96 (1965). Prikl. Fiz. 924,527; Ref. Akad. Soedin., No. https://doi.org/10.1007/BF01165434, Over 10 million scientific documents at your fingertips. Fiz. 2, p. 4. 2-Vinylpyridine is an organic compound with the formula CH 2 CHC 5 H 4 N. It is a derivative of pyridine with a vinyl group in the 2-position, next to the nitrogen. SYNTHESIS AND SOME CHEMICAL PROPERTIES OF 8-METHYL-3-HYDROXY-6-OXO-2H-3, S. S. Nametkin, V. M. Radionov, and N. N. Mel'nikov, in: Reactions and Methods of Khim.,30, 982 (1961). Check all that apply - Please note that only the first page is available if you have not selected a reading option after clicking "Read Article". Select data courtesy of the U.S. National Library of Medicine. and modeling of the electronic properties of the latter in order to obtain advanced materials for nanoelectronics. Ser. Ufa Scientific Center of the Russian Academy of Science, Oligomerization of alkynes by the RhCl3-aliquat 336 catalyst system Part 1. N. K. Kochetkov (ed. A. W. Schnizer and A. L. Stautzenberger, U. S. Patent No. Soc.,54, 1921 (1923). Zh. Zh. Process Engl.,17, 9 (1971). Zh. Read and print from thousands of top scholarly journals. A. Tschitschibabin, J. Prakt. Okadzaki, Japanese Patent No. Vereshchagin and 1. Bis(aquo)tetra(p-tolyl)porphinatocobalt(III) perchlorate reacted immediately with acetylene, in the absence and presence of tetra(p-tolyl)porphinatocobalt (II), to give a N,N′-vinylene linked bisporphyrin biscobalt(II) complex and a Co,N′-vinylene linked bisporphyrin cobalt(III) complex (4b), respectively. J. E. Mahan, U. S. Patent No. The collaborative research would allow extensive investigations into understanding the influence of the nature and structure of substituents in the dienoic acids, the introduction of additional functional substituents and various compounds of the “mitocan” group, as well as the location of the 5Z,9Z-dienic system position towards the carboxylic moiety on the antitumor activity. 2, pp. Abs.,45, 1628 (1951). S. S. Kukalenko, S. 1. 8, 8 (1973). Akad. Vada, Japanese Patent No. Otd. Abs., 47, 2685 (1953). A. E. Chichibabin, Zh. A. Nenz and M. Pieroni, Hydrocarbon Process,47, 103 (1968). Among these derivatives, there are compounds satisfying preclinical testing requirements and successfully overcame Preliminary Phase I-III Clinical Trials (22-methyl-5Z,9Z-haxacosadienoic acid, 14-methyl–5Z,9Z-pentadecadienoic acid, 23-methyl-5Z,9Z-tetracosadienoic acid) [Carballeira, N., 2008, Pommier et al., 2009, 2013].