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Igor A. Ushakov

Researcher at Russian Academy of Sciences

Publications -  490
Citations -  3706

Igor A. Ushakov is an academic researcher from Russian Academy of Sciences. The author has contributed to research in topics: Yield (chemistry) & Pyrrole. The author has an hindex of 25, co-authored 453 publications receiving 3201 citations. Previous affiliations of Igor A. Ushakov include Moscow State University & St. Petersburg State University of Telecommunications.

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Ethynylation of pyrroles with 1-acyl-2-bromoacetylenes on alumina: a formal ‘inverse Sonogashira coupling’

TL;DR: Pyrroles are cross-coupled with 1-acyl-2-bromoacetylenes on the surface of Al 2 O 3 at room temperature under solvent-free conditions to afford 2-(acylethynyl)pyrrole with 100% regioselectivity and in good yields as discussed by the authors.
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Transition-Metal-Free Superbase-Promoted Stereoselective α-Vinylation of Ketones with Arylacetylenes: A General Strategy for Synthesis of β,γ-Unsaturated Ketones

TL;DR: A wide variety of β,γ-unsaturated ketones of E configuration have been obtained in good to excellent yields via KO(t)Bu/DMSO promoted α-vinylation of aliphatic, cycloaliphatic and alkyl aromatic (heteroaromatic) ketones with diverse arylacetylenes.
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General Route to Symmetric and Asymmetric meso-CF3-3(5)-Aryl(hetaryl)- and 3,5-Diaryl(dihetaryl)-BODIPY Dyes

TL;DR: A general efficient route to hitherto inaccessible symmetric and asymmetric meso-CF(3)-BODIPy dyes has been developed and allows the BODIPY with 3(5)aryl(het Daryl) and 3,5-diaryl(hetaryl) substituents to be readily assembled.
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Base‐Catalyzed Stereoselective Vinylation of Ketones with Arylacetylenes: A New C(sp3)C(sp2) Bond‐Forming Reaction

TL;DR: Alkylaryl- and alkylheteroarylketones, including those with condensed aromatic moieties, are readily vinylated with arylacetylenes to give regio- and stereoselectively the (E)-beta-gamma-ethylenic ketones ((E)-3-buten-1-ones) in 61-84% yields and with approximately 100% stereoselectedivity.
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Selective, Metal-Free Approach to 3- or 5-CF3-Pyrazoles: Solvent Switchable Reaction of CF3-Ynones with Hydrazines

TL;DR: A detailed study of the reaction of trifluoroacetylated acetylenes and aryl (alkyl) hydrazines was performed, aimed to the regioselective synthesis of 3- or 5-trifluoromethylated pyrazoles, and it was found that the reguoselectivity of reaction depends dramatically on the solvent nature.