Diazatriphenylenes and their thiophene analogues: Synthesis and applications

This review highlights the recent advances in the field of the synthesis of diazatriphenylenes and their structural analogues, such as phenanthrenes, fused with the thiophene ring, and naphthalenes, condensed with two thiophene rings. Also applications of these compounds are considered. © ARKAT USA, Inc.The research was financially supported by the Russian Science Foundation (Project No. 16-13-10435) and the Russian Foundation for Basic Research (research project №. 17-03-00011-А)

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)

Cyano and CF3 Derivatives of 2-Aryl- and 2-Thienylquinazoline: Synthesis and Study of Optical Properties

This work was supported by the Russian Foundation for Basic Research (grant # 18-03-00112) and Russian Science Foundation (project # 19-73-10144)

An improved protocol for the preparation of 5, 11-dialkyl-6, 12-di(hetero)aryl-5, 11-dihydroindolo[3, 2-b]carbazoles and synthesis of their new 2, 8-dicyano-/2, 8-bis(benzo[d]thiazol-2-yl)-substituted derivatives

A number of 5, 11-dialkyl-6, 12-di(hetero)aryl-5, 11-dyhydroindolo[3, 2-b]carbazoles has been synthesized by modified method based on HBr catalyzed condensation of (hetero)aromatic aldehydes with indole in MeCN solution affording 5, 6, 11, 12-tetrahydroindolo[3, 2-b]carbazoles, that have been aromatized with I2 in DMF solution for 1 h at reflux, followed by alkylation of 5, 11-dihydro compounds. New 2, 8-dicyano-(10 examples) as well as 2, 8-bis(benzo[d]thiazol-2-yl)-substituted (5 examples) derivatives of these 5, 11-dyhydroindolo[3, 2-b]carbazoles have been obtained through their initial C2, 8-formylation, followed by treatment of dialdehydes with excess of hydroxylamine and dehydration of the formed aldoximes with acetic anhydride or by interaction with excess of 2-aminothiophenol in DMSO solution, respectively. © 2018 Arkat. All rights reserved.This research study was supported financially by the Russian Science Foundation (Project No. 16-13-10435)

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

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)

5-(Methylidene)barbituric acid as a new anchor unit for dye-sensitized solar cells (DSSC)

Novel dyes bearing a 5-(methylidene)barbituric acid moiety as a new acceptor/anchor fragment were obtained and exhibited remarkable photophysical properties, according to a preliminary assessment of their sensitization activity as elements for dye-sensitized solar cells. © ARKAT-USA, Inc

A convenient approach to the design and synthesis of indolo[3,2-c]coumarins via the microwave-assisted Cadogan reaction

3-(4,5-Dimethoxy-2-nitrophenyl)coumarins bearing various substituents on the benzene ring of the coumarin system have been prepared from salicylaldehydes and 2-(4,5-dimethoxy-2-nitrophenyl)acetonitrile by means of the Perkin condensation. Further cyclization of these 3-aryl coumarins through the microwave-assisted Cadogan reaction afforded the corresponding indolo[3,2-c]coumarins in good to excellent yields. © 2013 Elsevier Ltd. All rights reserved

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