Russian Chemical Bulletin (RUSS CHEM B+)
Publishing nearly 500 original articles a year by leading Scientists from Russia and throughout the world Russian Chemical Bulletin is a prominent international journal. The coverage of the journal spans practically all areas of fundamental chemical research and is presented in five sections: General and Inorganic Chemistry; Physical Chemistry; Organic Chemistry; Organometallic Chemistry; Chemistry of Natural Compounds and Bioorganic Chemistry. The Russian Chemical Bulletin 's International Advisory Board consists of eminent scientists from Europe USA and Japan. All papers are rigorously refereed and edited to the highest international standards. The Journal was founded in 1936 and has been published in English since 1951. 2001 celebrates the 50th year in publication of the Russian Chemical Bulletin's English edition. Please also check: http://rcb.ioc.ac.ru
- Impact factor0.38Show impact factor historyHide impact factor history
- WebsiteRussian Chemical Bulletin website
Other titlesIzvestii︠a︡ Akademii nauk. Serii︠a︡ khimicheskai︠a︡., Russian chemical bulletin, Izvestii︠a︡ Akademii nauk
Material typePeriodical, Internet resource
Document typeJournal / Magazine / Newspaper, Internet Resource
- Author can archive a pre-print version
- Author can archive a post-print version
- Authors own final version only can be archived
- Publisher's version/PDF cannot be used
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- Must link to publisher version
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- Articles in some journals can be made Open Access on payment of additional charge
Publications in this journal
Article: Silyl- and germylpropynals in the synthesis of azolyl-substituted 2-imidazoline 3-oxide 1-oxylsRussian Chemical Bulletin 02/2013; 58(9):1915-1920.
Russian Chemical Bulletin 02/2013; 55(3):591-592.
Russian Chemical Bulletin 02/2013; 53(6):1301-1304.
Article: Diastereoselective addition of organomanganese compounds to alpha-alkoxysubstituted propanalsRussian Chemical Bulletin 02/2013; 42(1):161 - 165.
Article: Polyfluorinated enamines. Synthesis of N-(3,3,3-trifluoro-2-trifluoromethylprop-1-enyl)ureaRussian Chemical Bulletin 02/2013; 45:482.
Article: Regioselectivity of N-substitution in bis-alkylation of 1,2,4-triazolo[1,5-a]benzimidazole-2-thione[show abstract] [hide abstract]
ABSTRACT: Cyclization of the corresponding N-substituted 1,2-diaminobenzimidazoles with carbon disulfide in refluxing DMF leads to 1-benzyl- and 3-methyl(benzyl)-1,2,4-triazolo[1,5- a]benzimidazole-2-thiones. Based on the results of their S-alkylation, quantum chemical calculations by the density functional theory method, and 1D and 2D NMR spectroscopic studies, it was concluded that the bis-alkylation of N-unsubstituted 1,2,4-triazolo[1,5- a]benzimidazole-2-thione in the presence of a base proceeds with the formation of N(4)- derivatives of 2-alkylthio-1,2,4-triazolo[1,5-a]benzimidazole, rather than N(3)-derivatives as was believed earlier.Russian Chemical Bulletin 06/2012;
Article: Chemiluminescence during interaction of 1,2,4-trioxolanes and 1,2,4,5-tetraoxanes with iron compounds[show abstract] [hide abstract]
ABSTRACT: The reaction of triterpene 1,2,4-trioxolanes with the system FeCl3-L-cysteine hydrochloride in the presence of rhodamine G is accompanied by chemiluminescence, whose emitter is an excited dye molecule. Light emission was also found in the biologically important reaction of 1,2,4,5-tetraoxanes with Fe2+ ions in aqueous acetonitrile. Key wordstrioxolanes–tetraoxanes–chemiluminescence–triterpenoidsRussian Chemical Bulletin 05/2012; 60(2):373-375.
Article: New organic picolylamine-type ligands and electrochemical study of their complexation with Cu(MeCN)4ClO4[show abstract] [hide abstract]
ABSTRACT: A series of novel organic ligands with dipicolylamine and disulfide groups connected by polymethylene, alkylaryl, alkoxyaryl, or alkoxycarbonyl linker was synthesized. The electrochemical study by cyclic voltammetry was carried out for two synthesized ligands, and the formation of the complexes with Cu(MeCN)ClO4 in the solution or on the gold electrode surface was established. The complex of CuI with 1,24-bis[N,N-bis(2-pyridylmethyl)-glycinoyloxy]-12,13-dithiatetracosane chemisorbed on the Au electrode is capable of binding molecular oxygen from solution. Key wordsdipicolylamines–disulfides–copper(I) complexes–chemisorption–gold–cyclic voltammetryRussian Chemical Bulletin 05/2012; 60(2):261-268.
Data provided are for informational purposes only. Although carefully collected, accuracy cannot be guaranteed. The impact factor represents a rough estimation of the journal's impact factor and does not reflect the actual current impact factor. Publisher conditions are provided by RoMEO. Differing provisions from the publisher's actual policy or licence agreement may be applicable.
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