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Roman A. Irgashev

Researcher at Russian Academy of Sciences

Publications -  96
Citations -  754

Roman A. Irgashev is an academic researcher from Russian Academy of Sciences. The author has contributed to research in topics: Trifluoromethyl & Indole test. The author has an hindex of 15, co-authored 91 publications receiving 660 citations. Previous affiliations of Roman A. Irgashev include Enamine Ltd & Ural State University.

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One-pot three-component reaction of 3-(polyfluoroacyl)chromones with active methylene compounds and ammonium acetate: regioselective synthesis of novel RF-containing nicotinic acid derivatives

TL;DR: In this article, the C-2 atom of the chromone system with pyrone ring-opening and subsequent cyclization to 5-salicyloyl-2-methyl-5-(polyfluoroalkyl)-5H-chromeno[4,3-b]pyridine-3-carbonitriles was investigated.
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3-(Polyhaloacyl)chromones and their Hetero Analogues: Synthesis and Reactions with Amines

TL;DR: 2-Hydroxy-2-(polyhaloalkyl)chroman-4-ones react with diethoxymethyl acetate at 140-150 °C for 15 minutes to give 3-(poly-haloacyl)chromones in good yields as discussed by the authors.
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Methyl 2-methoxytetrafluoropropionate as a synthetic equivalent of methyl trifluoropyruvate in the Claisen condensation. The first synthesis of 2-(trifluoroacetyl)chromones and 5-aryl-2-hydroxy-2-(trifluoromethyl)furan-3(2H)-ones

TL;DR: In this article, 2-(Trifluoroacetyl)chromones and 5-aryl-2-hydroxy-2-(trifluoromethyl)furan-3(2H)-chromones were obtained via the Claisen condensation of acetophenones with methyl 2-methoxytetrafluoropropionate, followed by sulfuric acid-mediated deprotection of the reaction products.
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Construction of Heteroacenes with Fused Thiophene and Pyrrole Rings via the Fischer Indolization Reaction

TL;DR: The protocol suggested for preparing these N,S-heteroacenes is based on using easily available reagents, such as cinnamic acids and arylhydrazines, which can be involved in the Fischer indole synthesis, as the key step.