T. E. Glotova - Concepedia

Author

T. E. Glotova

A.E. Favorsky Irkutsk Institute of Chemistry

Also Known As

Glotova, T.E., Glotova, Tatyana E., Glotova, Tat’yana E., T. E. GLOTOVA, T. E. Glotova, Tatyana E. Glotova, Tatyana Glotova, Tatýana Glotova, Tat’yana E. Glotova

109

Publications

295

Citations

H-Index

Concepts

All Affiliations

A.E. Favorsky Irkutsk Institute of Chemistry Russian Academy of Sciences Institute of Problems of Chemical Physics

About

T. E. Glotova is an author at A.E. Favorsky Irkutsk Institute of Chemistry specializing in organic chemistry, chemistry, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	7	7	121
2	Biomolecular Engineering	4	4	77
3	Chemical Engineering	4	4	62
4	Natural Sciences	2	2	39
5	Biochemistry	2	2	39

T. E. Glotova

Publications

181

Citations

H-Index

Page 1

	Year	Citations
Chemo-, regio- and stereospecific addition of amino acids to acylacetylenes: a facile synthesis of new N-acylvinyl derivatives of amino acids T. E. Glotova, Marina Yu. Dvorko, Igor А. Ushakov, Tetrahedron EngineeringAmino AcidsBiochemistryNatural SciencesFacile Synthesis	2009	24
Expedient one-step synthesis of nitrogen stilbene analogs by transition metal-free hydroamination of arylacetylenes with pyrroles Marina Yu. Dvorko, Elena Yu. Schmidt, T. E. Glotova, Tetrahedron Chemical EngineeringExpedient One-step SynthesisEngineeringNovel OrganocatalystsTransition Metal-free Hydroamination	2012	22
Triphenylphosphine as an effective catalyst for ketoximes addition to acylacetylenes: regio- and stereospecific synthesis of (E)-(O)-2-(acyl)vinylketoximes T. E. Glotova, Marina Yu. Dvorko, Igor А. Ushakov, Tetrahedron Enantioselective SynthesisEngineeringStereospecific SynthesisAlkene MetathesisEffective Catalyst	2010	20
1,3-Dipolar cycloaddition of 3-phenylamino-5-phenylimino-1,2,4-dithiazole to 1-acyl-2-phenylacetylenes—A new route to functionalized 1,3-thiazole derivatives T. E. Glotova, Marina Yu. Dvorko, A. I. Albanov, Russian Journal of Organic Chemistry	2008	20
Base Catalyzed Double Addition of Secondary Phosphine Chalcogenides to Benzoylacetylene T. E. Glotova, Marina Yu. Dvorko, S. N. Arbuzova, Letters in Organic Chemistry Koh-thf SuspensionChemical EngineeringDerivative (Chemistry)EngineeringSecondary Phosphine Chalcogenides	2007	18
Reaction of secondary phosphine oxides with acylacetylenes Marina Yu. Dvorko, T. E. Glotova, Igor А. Ushakov, Russian Journal of Organic Chemistry	2010	18
Chemo- and Regiospecific Monoaddition of Secondary Phosphine Sulfides to 1-Acyl-2-phenylacetylenes T. E. Glotova, Marina Yu. Dvorko, Nina K. Gusarova, Phosphorus, sulfur, and silicon and the related elements EngineeringAlkene MetathesisBiochemistryNatural SciencesMild Conditions	2008	15
Stereoselective reduction of 1-acyl-2-phenylacetylenes with triphenylphosphine in water: efficient synthesis of E-chalcones S. N. Arbuzova, T. E. Glotova, Marina Yu. Dvorko, ARKIVOC High YieldsRoom TemperatureChemical EngineeringOrganic SolventEngineering	2011	12
Synthesis of 3,3-dimethyl-2-phenyl-3H-pyrrole from Isopropyl Phenyl Ketoxime and Acetylene: A Side Formation of 4,4-dimethyl-5-phenyl-1-vinyl-2-pyrrolidinone as Clue to the Reaction Mechanism Dmitrii A. Shabalin, T. E. Glotova, Elena Yu. Schmidt, Mendeleev Communications	2014	11
Synthesis of О-2-(acyl)vinylketoximes and their unusual rearrangements into 2- and 3-acyl-substituted pyrroles T. E. Glotova, Elena Yu. Schmidt, Marina Yu. Dvorko, Tetrahedron Letters Unusual Rearrangements3-Acyl-substituted PyrrolesHeterocyclicOrganic ChemistryChemistry	2010	11

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