Cyclotrimerization of 3-R-1,2,4-triazin-5(4H)-ones with cyclic ketones

New heterocyclic tetracyclic systems were synthesized. Interaction between 3-R-1,2,4-triazin-5(4H)-ones and cyclic ketones under acidic conditions leads to the formation of zwitterion derivatives of 5,6,7,8,9,10,11,12-octahydro-[1,2,4] triazino[1,6- f ]phenanthridine and 1,2,3,6,7,8-hexahydro-bicyclopenta[b,d] pyrido[1,2- f ][1,2,4]triazine. © 2010 Verlag der Zeitschrift für Naturforschung, Tübingen

Chemodivergence in Metal-Catalyzed Cross-Dehydrogenative Coupling Reactions of 2H-imidazole 1-oxides with 1H-pyrrole

This work was supported by the Russian Science Foundation (Project # 18-73-00088)

Synthesis of chiral ferrocenylazines. Negishi cross-coupling or S N H reactions?

Preparation of new hetaryl-containing planar chiral ferrocene by a nucleophilic substitution of hydrogen in azines was performed using a lithium derivative of (S)-ferrocenyl-p-tolylsulfoxide as s nucleophilic reagent © 2013 Pleiades Publishing, Ltd

Synthesis of 4-hydroxy and 6-hydroxyindoles: a renaissance of the Bischler reaction

In the present work we studied a modified Bischler-Möhlau reaction – synthesis of indoles from benzoin and aniline. Our proposed modification of this method differs from that described earlier in that the reaction is carried out at a lower temperature, which makes it possible to improve yields and reduce formation of tarry side products. In addition, unlike the previous contradictory works, which described the preparation of a single 4-hydroxy or 6-hydroxy isomer in condensation of m-aminophenol and benzoin, we obtained both 4-hydroxy and 6-hydroxy isomers

Nucleophilic Addition of Indoles to Carborancarboxaldehyde – a Convinient Synthetic Strategy Towards Novel Boron-Enriched 3-Indolylmethanols

This work was supported by Russian Science Foundation (Project 18-13-00365)

Nucleophilic Substitution of Hydrogen (SNH) as a Synthetic Approach Towards Pentafluorophenyl SubstituteD 2himidazoles, 1,2,3-triazoles and its N-oxides

The study was carried out with the financial support of the Russian Science Foundation as part of a research project 18-73-00088

Cyclic peroxides and related initiating systems for radical polymerization of methyl methacrylate

Cyclic peroxides as initiators for the radical polymerization of methyl methacrylate were proposed. The initial rates, initiation rates, and effective activation energies of polymerization initiated by cyclic peroxides and cyclic peroxide-1-pyridyl-2-ferrocene systems were determined. The radical yields to the volume upon the thermal decomposition of cyclic peroxides and their catalytic decomposition in the presence of 1-pyridyl-2-ferrocene were determined. In combination with 1-pyridyl-2-ferrocene cyclic peroxides form efficient initiating systems favoring an increase in the polymerization rate, a decrease in the molecular weights, and an increase in syndiotacticity of the synthesized poly(methyl methacrylate). © 2013 Springer Science+Business Media New York

MECHANOCHEMICAL CROSS DEHYDROGENATIVE COUPLING: SYNTHESES OF VARIOUS ORGANIC MOLECULES

S. Santra is thankful to the Russian Science Foundation (ref # 20-73-10205) for funding

Stable σh-adducts in the reactions of the acridinium cation with heterocyclic N-nucleophiles

A reaction of NH-heterocycles with the 10-methylacridinium cation in the presence of a base led to 9,10-dihydro-10-methyl-9-substituted acridines, which can be considered as stable intermediates in the aromatic nucleophilic substitution reaction of hydrogen. The structure of the intermediates was studied and their oxidation potentials were determined. Generally, the oxidation potential was found to symbatically change with the changes in the energy of HOMO. © 2013 Springer Science+Business Media New York