Enantioselective Cycloaddition Reactions Catalyzed by BINOL-Derived Phosphoric Acids and N-Triflyl Phosphoramides: Recent AdvancesSynthesis and Electrochemical and Photophysical Characterization of New 4,4'-π-Conjugated 2,2'-Bipyridines that are End-Capped with Cyanoacrylic Acid/Ester GroupsSpontaneous mirror symmetry breaking in the aldol reaction and its potential relevance in prebiotic chemistry.Recent progress in the development of synthetic hybrids of natural or unnatural bioactive compounds for medicinal chemistry.Enantioselective epoxidation of electron-deficient olefins: an organocatalytic approach.Bifunctional primary amine-thioureas in asymmetric organocatalysis.Artemisinin-Derived Dimers: Potent Antimalarial and Anticancer Agents.New efficient artemisinin derived agents against human leukemia cells, human cytomegalovirus and Plasmodium falciparum: 2nd generation 1,2,4-trioxane-ferrocene hybrids.The broad-spectrum antiinfective drug artesunate interferes with the canonical nuclear factor kappa B (NF-κB) pathway by targeting RelA/p65.Synthesis and study of cytotoxic activity of 1,2,4-trioxane- and egonol-derived hybrid molecules against Plasmodium falciparum and multidrug-resistant human leukemia cells.Facile access to potent antiviral quinazoline heterocycles with fluorescence properties via merging metal-free domino reactions.Generation of Complex Azabicycles and Carbobicycles from Two Simple Compounds in a Single Operation through a Metal-Free Six-Step Domino Reaction.Highly potent artemisinin-derived dimers and trimers: Synthesis and evaluation of their antimalarial, antileukemia and antiviral activities.Cytotoxic profiling of artesunic and betulinic acids and their synthetic hybrid compound on neurons and gliomas.Deeper Insight into the Six-Step Domino Reaction of Aldehydes with Malononitrile and Evaluation of Antiviral and Antimalarial Activities of the Obtained Bicyclic Products.Synthesis and evaluation of new guanidine-thiourea organocatalyst for the nitro-Michael reaction: Theoretical studies on mechanism and enantioselectivity.Demonstration of "Möbius" aromaticity in planar metallacycles.Asymmetric hydrocyanation of hydrazones catalyzed by in situ formed O-silylated BINOL-phosphate: a convenient access to versatile alpha-hydrazino acids.Enantioselective nitro-Michael reactions catalyzed by short peptides on water.Thiourea-based non-nucleoside inhibitors of HIV reverse transcriptase as bifunctional organocatalysts in the asymmetric Strecker synthesis.Highly enantioselective organocatalytic formation of a quaternary carbon center via chiral Brønsted acid catalyzed self-coupling of enamides.Synthesis of Novel Hybrids of Thymoquinone and Artemisinin with High Activity and Selectivity Against Colon Cancer.Evidence for an enol mechanism in a highly enantioselective Mannich-type reaction catalyzed by primary amine-thiourea.Spontaneous emergence of homochirality via coherently coupled antagonistic and reversible reaction cycles.Demonstration of spontaneous chiral symmetry breaking in asymmetric Mannich and Aldol reactions.In Vivo and In Vitro Optimization of Screening Antimalarial Hits toward Lead Molecules for Preclinical Development.A new architecture for high spin organics based on Baird's rule of 4n electron triplet aromatics.Iron-Catalyzed Olefin Metathesis with Low-Valent Iron Alkylidenes.Artesunate-derived monomeric, dimeric and trimeric experimental drugs - Their unique mechanistic basis and pronounced antiherpesviral activity.Three-Component Domino Knoevenagel/Vinylogous Michael Reaction: Entry to Challenging o-Terphenyls.Treatment of Multidrug-Resistant Leukemia Cells by Novel Artemisinin-, Egonol-, and Thymoquinone-Derived Hybrid Compounds.Novel Fully Organic Water Oxidation Electrocatalysts: A Quest for Simplicity.Synthesis of artemisinin-derived di/tri-mers and dendrimers, investigation of their activity against P. falciparum and cytomegalovirus, and insights into their mechanisms of action.Synthesis of Novel Hybrids of Quinazoline and Artemisinin with High Activities against Plasmodium falciparum, Human Cytomegalovirus, and Leukemia Cells.New artesunic acid homodimers: Potent reversal agents of multidrug resistance in leukemia cellsSpin-paired solvated electron couples in alkali-ammonia systemsCombination of 5-fluorouracil and thymoquinone targets stem cell gene signature in colorectal cancer cellsFirst enantioselective organocatalytic allylation of simple aldimines with allyltrichlorosilaneEvidence of asymmetric autocatalysis in organocatalytic reactionsAsymmetric synthesis of β-adrenergic blockers through multistep one-pot transformations involving in situ chiral organocatalyst formation
P50
Q26781415-56C5B9E5-E297-4D5F-95B7-BD5023ED01E9Q28595836-31B110D5-7479-474C-A4E2-B4A7DD949836Q33348178-8736C8F7-A922-4BC8-9377-07CF61FBD523Q37682263-52B7F93F-FA48-4590-8A13-EEAD3ADA463EQ37838878-7A751FA3-46C1-4BBF-ADC9-E446F86E136EQ38140730-1B2B3B70-D83B-4E01-ABBD-CDAA1800B2CEQ38787292-1E0417E8-1E4F-45EA-A102-0736EE3B78EFQ38876027-60EC95C3-FA58-4C65-99CE-F9888DDC1CBAQ38945153-1DD9711D-89C0-4915-8F2A-16457F82DD90Q39391701-B4DA2B4E-5A7F-4C54-A5A2-5A8AE9329CE1Q40219149-EC4C2275-DB68-48C0-B72A-79806D3C1899Q40885277-0F2A291A-01DA-47C7-BBD8-BB307E66BE3EQ41496256-50D5F72E-B9BB-43BD-9AE9-FA67E87C21EBQ41845885-A18FA433-D84B-4E83-8C93-64F5FE23D83EQ41912476-3DD5997D-22AC-4609-B036-2D5890DC2EB5Q42608736-8F81D670-433E-4E28-8731-8722ACCF910AQ43055905-B314E68E-4224-43D5-BE7F-EBE13928D935Q43233010-4EE6CC19-20E0-4975-B1B8-C7460DF94242Q43268835-6A661898-1424-47F8-BE0D-AF0D76C54450Q44571045-F209EB13-6159-4901-8624-6A8C16D23E4AQ46348388-54AA2D74-554B-4D94-8F2A-8A8E05EF0B01Q46446158-53116603-5887-4BCF-9097-CE3FC5790F58Q46469858-43E77411-85B8-4537-8D6D-68E94458380EQ47840124-32CE301D-3E17-4CA9-81B9-2D3D71BFFCADQ47841969-B4C50208-F925-4B8C-9A98-35A5B284ED5CQ47975899-426A5A04-CDC5-4651-8F3F-7D3CE8EF331CQ48048740-E07B4113-DF22-42DC-8B5C-AEBC2D808227Q48059623-A6A7FCC7-0339-4099-8CE6-281D727F873AQ49847044-3480C8AA-061A-45F6-AD52-1E2436653E49Q50083825-F993DE2A-F793-49CE-A267-91938C383CFDQ52593710-5ACBF410-76E5-44EB-801B-8503274C60DDQ52603488-C0FFBE3C-68E8-4EAF-85A0-B56FCCBB4545Q52640324-9952AB98-CB17-45F5-8CEC-292E3C908E56Q55710636-F979668E-6DB0-48DB-8012-AD1360E8A83AQ58595714-2063D330-5F25-45CF-BB2C-2DF83C7855A4Q58611919-B7DC80E4-2048-4B68-8893-BBCB70433586Q64053377-44DE1B3A-FA38-4C0E-B6B2-39B6489B5B00Q79363928-D1239430-5054-4988-B63A-BED3664B175CQ79405982-D3A149F7-F20E-41C2-949B-50B57AE66D94Q82664288-2CB4C742-2292-4AB4-9D02-7EB471530C0C
P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
ricercatrice
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russische Chemikerin und Hochschullehrerin
@de
հետազոտող
@hy
name
Svetlana B Tsogoeva
@ast
Svetlana B Tsogoeva
@en
Svetlana B Tsogoeva
@es
Svetlana B Tsogoeva
@nl
Svetlana Tsogoeva
@de
type
label
Svetlana B Tsogoeva
@ast
Svetlana B Tsogoeva
@en
Svetlana B Tsogoeva
@es
Svetlana B Tsogoeva
@nl
Svetlana Tsogoeva
@de
prefLabel
Svetlana B Tsogoeva
@ast
Svetlana B Tsogoeva
@en
Svetlana B Tsogoeva
@es
Svetlana B Tsogoeva
@nl
Svetlana Tsogoeva
@de
P214
P227
P106
P1153
6603139295
P21
P214
P227
P31
P496
0000-0003-4845-0951
P569
1973-01-01T00:00:00Z
P7859
viaf-20873727