| Year |
Citation |
Score |
| 2021 |
Grau BW, Dill M, Hampel F, Kahnt A, Jux N, Tsogoeva SB. Four-step domino reaction enables fully controlled non-statistical synthesis of hexaarylbenzene with six different aryl groups. Angewandte Chemie (International Ed. in English). PMID 34060211 DOI: 10.1002/anie.202104437 |
0.319 |
|
| 2020 |
Hahn F, Niesar A, Wangen C, Wild M, Grau B, Herrmann L, Capci A, Adrait A, Couté Y, Tsogoeva SB, Marschall M. Target verification of artesunate-related antiviral drugs: assessing the role of mitochondrial and regulatory proteins by click chemistry and fluorescence labeling. Antiviral Research. 104861. PMID 32590041 DOI: 10.1016/J.Antiviral.2020.104861 |
0.307 |
|
| 2020 |
Tortora C, Mai C, Cascella F, Mauksch M, Seidel-Morgenstern A, Lorenz H, Tsogoeva SB. Speeding up Viedma Deracemization through Water catalyzed and Reactant Self-catalyzed Racemization. Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry. PMID 32519414 DOI: 10.1002/Cphc.202000493 |
0.358 |
|
| 2020 |
Çapcı A, Lorion MM, Mai C, Hahn F, Hodek J, Wangen C, Weber J, Marschall M, Ackermann L, Tsogoeva SB. (Iso)Quinoline-Artemisinin Hybrids via Click Chemistry: Highly Potent Agents against Viruses. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32485071 DOI: 10.1002/Chem.202001803 |
0.369 |
|
| 2019 |
Belletti G, Tortora C, Mellema ID, Tinnemans P, Meekes H, Rutjes FPJT, Tsogoeva SB, Vlieg E. Photoracemization-Based Viedma Ripening of a BINOL Derivative. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31663650 DOI: 10.1002/Chem.201904382 |
0.318 |
|
| 2019 |
Fingerhut A, Vargas-Caporali J, Leyva-Ramírez MA, Juaristi E, Tsogoeva SB. Biomimetic Non-Heme Iron-Catalyzed Epoxidation of Challenging Terminal Alkenes Using Aqueous HO as an Environmentally Friendly Oxidant. Molecules (Basel, Switzerland). 24. PMID 31480640 DOI: 10.3390/Molecules24173182 |
0.359 |
|
| 2019 |
Çapcı A, Lorion MM, Wang H, Simon N, Leidenberger M, Silva MCB, Moreira DRM, Yongping Z, Yuqing M, Jia Yun C, Mun Lee Y, Friedrich O, Kappes B, Wang J, Ackermann L, ... Tsogoeva SB, et al. Artemisinin-(Iso)Quinoline Hybrids by C-H Activation and Click Chemistry: Combating Multidrug-Resistant Malaria. Angewandte Chemie (International Ed. in English). PMID 31290221 DOI: 10.1002/Anie.201907224 |
0.316 |
|
| 2019 |
Mauksch M, Tsogoeva SB. Hückel and Möbius Aromaticity in Charged Sigma Complexes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30969449 DOI: 10.1002/Chem.201900849 |
0.329 |
|
| 2019 |
Guryev AA, Hahn F, Marschall M, Tsogoeva SB. Visible-Light-Driven C-H Oxidation of Cyclic Tertiary Amines: Access to Synthetic Strychnos Alkaloids with Antiviral Activity. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30620121 DOI: 10.1002/Chem.201900078 |
0.31 |
|
| 2019 |
Grau BW, Bönisch S, Neuhauser A, Hampel F, Görling A, Tsogoeva SB. Facile Access to Challenging
ortho
‐Terphenyls via Merging Two Multi‐Step Domino Reactions in One‐Pot: A Joint Experimental/Theoretical Study Chemcatchem. 11: 3982-3992. DOI: 10.1002/Cctc.201900746 |
0.332 |
|
| 2018 |
Karagöz AÇ, Leidenberger M, Hahn F, Hampel F, Friedrich O, Marschall M, Kappes B, Tsogoeva SB. Synthesis of new betulinic acid/betulin-derived dimers and hybrids with potent antimalarial and antiviral activities. Bioorganic & Medicinal Chemistry. PMID 30503412 DOI: 10.1016/J.Bmc.2018.11.018 |
0.339 |
|
| 2018 |
Fröhlich T, Kiss A, Wölfling J, Mernyák E, Kulmány ÁE, Minorics R, Zupkó I, Leidenberger M, Friedrich O, Kappes B, Hahn F, Marschall M, Schneider G, Tsogoeva SB. Synthesis of Artemisinin-Estrogen Hybrids Highly Active against HCMV, , and Cervical and Breast Cancer. Acs Medicinal Chemistry Letters. 9: 1128-1133. PMID 30429957 DOI: 10.1021/Acsmedchemlett.8B00381 |
0.301 |
|
| 2018 |
Fröhlich T, Reiter C, Saeed MEM, Hutterer C, Hahn F, Leidenberger M, Friedrich O, Kappes B, Marschall M, Efferth T, Tsogoeva SB. Synthesis of Thymoquinone-Artemisinin Hybrids: New Potent Antileukemia, Antiviral, and Antimalarial Agents. Acs Medicinal Chemistry Letters. 9: 534-539. PMID 29937978 DOI: 10.1021/Acsmedchemlett.7B00412 |
0.368 |
|
| 2018 |
Çapcı Karagöz A, Reiter C, Seo EJ, Gruber L, Hahn F, Leidenberger M, Klein V, Hampel F, Friedrich O, Marschall M, Kappes B, Efferth T, Tsogoeva SB. Access to new highly potent antileukemia, antiviral and antimalarial agents via hybridization of natural products (homo)egonol, thymoquinone and artemisinin. Bioorganic & Medicinal Chemistry. PMID 29887512 DOI: 10.1016/J.Bmc.2018.05.041 |
0.333 |
|
| 2018 |
Fröhlich T, Hahn F, Belmudes L, Leidenberger M, Friedrich O, Kappes B, Couté Y, Marschall M, Tsogoeva SB. 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. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29570874 DOI: 10.1002/Chem.201800729 |
0.348 |
|
| 2018 |
Hahn F, Fröhlich T, Frank T, Bertzbach LD, Kohrt S, Kaufer BB, Stamminger T, Tsogoeva SB, Marschall M. Artesunate-derived monomeric, dimeric and trimeric experimental drugs - Their unique mechanistic basis and pronounced antiherpesviral activity. Antiviral Research. PMID 29458133 DOI: 10.1016/J.Antiviral.2018.02.013 |
0.336 |
|
| 2018 |
Grau D, Grau BW, Hampel F, Tsogoeva SB. Three-Component Domino Knoevenagel/Vinylogous Michael Reaction: Entry to Challenging o-Terphenyls. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29325200 DOI: 10.1002/Chem.201800048 |
0.394 |
|
| 2018 |
Grau D, Grau BW, Hampel F, Tsogoeva SB. Frontispiece: Three-Component Domino Knoevenagel/Vinylogous Michael Reaction: Entry to Challenging o
-Terphenyls Chemistry - a European Journal. 24. DOI: 10.1002/Chem.201882564 |
0.301 |
|
| 2017 |
Bock CM, Parameshwarappa G, Bönisch S, Bauer W, Hutterer C, Leidenberger M, Friedrich O, Marschall M, Kappes B, Görling A, Tsogoeva SB. Deeper Insight into the Six-Step Domino Reaction of Aldehydes with Malononitrile and Evaluation of Antiviral and Antimalarial Activities of the Obtained Bicyclic Products. Chemistryopen. 6: 364-374. PMID 28638769 DOI: 10.1002/Open.201700005 |
0.41 |
|
| 2017 |
Mauksch M, Tsogoeva SB. Iron-Catalyzed Olefin Metathesis with Low-Valent Iron Alkylidenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 23: 10264-10269. PMID 28618111 DOI: 10.1002/Chem.201702276 |
0.317 |
|
| 2017 |
Held FE, Guryev AA, Fröhlich T, Hampel F, Kahnt A, Hutterer C, Steingruber M, Bahsi H, von Bojničić-Kninski C, Mattes DS, Foertsch TC, Nesterov-Mueller A, Marschall M, Tsogoeva SB. Facile access to potent antiviral quinazoline heterocycles with fluorescence properties via merging metal-free domino reactions. Nature Communications. 8: 15071. PMID 28462939 DOI: 10.1038/Ncomms15071 |
0.345 |
|
| 2017 |
Held FE, Stingl KA, Tsogoeva SB. Synthesis of (R)-Modafinil via Organocatalyzed and Non-Heme Iron-Catalyzed Sulfoxidation Using H2O2 as an Environmentally Benign Oxidant Symmetry. 9: 88. DOI: 10.3390/Sym9060088 |
0.39 |
|
| 2017 |
Bock CM, Parameshwarappa G, Bönisch S, Bauer W, Hutterer C, Leidenberger M, Friedrich O, Marschall M, Kappes B, Görling A, Tsogoeva SB. Back Cover: Deeper Insight into the Six-Step Domino Reaction of Aldehydes with Malononitrile and Evaluation of Antiviral and Antimalarial Activities of the Obtained Bicyclic Products (ChemistryOpen 3/2017) Chemistryopen. 6: 452-452. DOI: 10.1002/Open.201700092 |
0.377 |
|
| 2016 |
Fröhlich T, Ndreshkjana B, Muenzner JK, Reiter C, Hofmeister E, Mederer S, Fatfat M, El-Baba C, Gali-Muhtasib H, Schneider-Stock R, Tsogoeva SB. Synthesis of Novel Hybrids of Thymoquinone and Artemisinin with High Activity and Selectivity Against Colon Cancer. Chemmedchem. PMID 27973725 DOI: 10.1002/Cmdc.201600594 |
0.305 |
|
| 2016 |
Mauksch M, Tsogoeva SB. Duality of Orbital-Symmetry-Allowed Transition States for Thermal Sigmatropic Hydrogen Shifts in Transition Metal Compounds. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 13916-13926. PMID 27515407 DOI: 10.1002/Chem.201602499 |
0.302 |
|
| 2016 |
Fingerhut A, Wu Y, Kahnt A, Bachmann J, Tsogoeva SB. Synthesis and Electrochemical and Photophysical Characterization of New 4,4'-π-Conjugated 2,2'-Bipyridines that are End-Capped with Cyanoacrylic Acid/Ester Groups. Chemistry, An Asian Journal. 11: 1232-1239. PMID 27101254 DOI: 10.1002/Asia.201501324 |
0.304 |
|
| 2016 |
Fröhlich T, Çapcı Karagöz A, Reiter C, Tsogoeva SB. Artemisinin-Derived Dimers: Potent Antimalarial and Anticancer Agents. Journal of Medicinal Chemistry. 59: 7360-88. PMID 27010926 DOI: 10.1021/Acs.Jmedchem.5B01380 |
0.363 |
|
| 2016 |
Bock CM, Parameshwarappa G, Bönisch S, Neiss C, Bauer W, Hampel F, Görling A, Tsogoeva SB. Generation of Complex Azabicycles and Carbobicycles from Two Simple Compounds in a Single Operation through a Metal-Free Six-Step Domino Reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 5189-97. PMID 26919489 DOI: 10.1002/Chem.201504798 |
0.414 |
|
| 2016 |
Tsogoeva S, Jalani H, Karagöz A. Synthesis of Substituted 1,2,3-Triazoles via Metal-Free Click Cycloaddition Reactions and Alternative Cyclization Methods Synthesis. 49: 29-41. DOI: 10.1055/S-0036-1588904 |
0.431 |
|
| 2016 |
Held FE, Tsogoeva SB. Asymmetric cycloaddition reactions catalyzed by bifunctional thiourea and squaramide organocatalysts: recent advances Catalysis Science & Technology. 6: 645-667. DOI: 10.1039/C5Cy01894C |
0.387 |
|
| 2016 |
Bock CM, Parameshwarappa G, Bönisch S, Neiss C, Bauer W, Hampel F, Görling A, Tsogoeva SB. Inside Back Cover: Generation of Complex Azabicycles and Carbobicycles from Two Simple Compounds in a Single Operation through a Metal-Free Six-Step Domino Reaction (Chem. Eur. J. 15/2016) Chemistry - a European Journal. 22: 5431-5431. DOI: 10.1002/Chem.201600644 |
0.35 |
|
| 2015 |
Hutterer C, Niemann I, Milbradt J, Fröhlich T, Reiter C, Kadioglu O, Bahsi H, Zeitträger I, Wagner S, Einsiedel J, Gmeiner P, Vogel N, Wandinger S, Godl K, Stamminger T, ... ... Tsogoeva SB, et al. The broad-spectrum antiinfective drug artesunate interferes with the canonical nuclear factor kappa B (NF-κB) pathway by targeting RelA/p65. Antiviral Research. PMID 26546752 DOI: 10.1016/J.Antiviral.2015.10.003 |
0.304 |
|
| 2015 |
Held FE, Grau D, Tsogoeva SB. Enantioselective Cycloaddition Reactions Catalyzed by BINOL-Derived Phosphoric Acids and N-Triflyl Phosphoramides: Recent Advances. Molecules (Basel, Switzerland). 20: 16103-26. PMID 26404222 DOI: 10.3390/Molecules200916103 |
0.424 |
|
| 2015 |
Reiter C, Fröhlich T, Zeino M, Marschall M, Bahsi H, Leidenberger M, Friedrich O, Kappes B, Hampel F, Efferth T, Tsogoeva SB. New efficient artemisinin derived agents against human leukemia cells, human cytomegalovirus and Plasmodium falciparum: 2nd generation 1,2,4-trioxane-ferrocene hybrids. European Journal of Medicinal Chemistry. 97: 164-72. PMID 25965779 DOI: 10.1016/J.Ejmech.2015.04.053 |
0.318 |
|
| 2015 |
Fingerhut A, Serdyuk OV, Tsogoeva SB. Non-heme iron catalysts for epoxidation and aziridination reactions of challenging terminal alkenes: towards sustainability Green Chemistry. 17: 2042-2058. DOI: 10.1039/C4Gc02413C |
0.314 |
|
| 2014 |
Reiter C, Capcı Karagöz A, Fröhlich T, Klein V, Zeino M, Viertel K, Held J, Mordmüller B, Emirdağ Öztürk S, Anıl H, Efferth T, Tsogoeva SB. 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. European Journal of Medicinal Chemistry. 75: 403-12. PMID 24561670 DOI: 10.1016/J.Ejmech.2014.01.043 |
0.318 |
|
| 2014 |
Held FE, Wei S, Eder K, Tsogoeva SB. One-pot route to β-adrenergic blockers via enantioselective organocatalysed epoxidation of terminal alkenes as a key step Rsc Adv.. 4: 32796-32801. DOI: 10.1039/C4Ra04011B |
0.371 |
|
| 2014 |
Ibrahim MM, Grau D, Hampel F, Tsogoeva SB. α-Nitro Epoxides in Organic Synthesis: Development of a One-Pot Organocatalytic Strategy for the Synthesis of Quinoxalines European Journal of Organic Chemistry. 2014: 1401-1405. DOI: 10.1002/Ejoc.201301591 |
0.378 |
|
| 2013 |
Serdyuk OV, Heckel CM, Tsogoeva SB. Bifunctional primary amine-thioureas in asymmetric organocatalysis. Organic & Biomolecular Chemistry. 11: 7051-71. PMID 24057617 DOI: 10.1039/C3Ob41403E |
0.379 |
|
| 2012 |
Shubina TE, Freund M, Schenker S, Clark T, Tsogoeva SB. Synthesis and evaluation of new guanidine-thiourea organocatalyst for the nitro-Michael reaction: Theoretical studies on mechanism and enantioselectivity. Beilstein Journal of Organic Chemistry. 8: 1485-98. PMID 23019483 DOI: 10.3762/Bjoc.8.168 |
0.394 |
|
| 2012 |
Tsogoeva S, Wei S, Weiß K. Convenient One-Pot Two-Step Synthesis of 1,3-Thiazoles via Organocatalyzed Epoxidation of Nitroolefins Synthesis. 44: 3441-3446. DOI: 10.1055/S-0031-1291139 |
0.401 |
|
| 2012 |
Held FE, Fingerhut A, Tsogoeva SB. Insights into the spontaneous emergence of enantioselectivity in an asymmetric Mannich reaction carried out without external catalyst Tetrahedron: Asymmetry. 23: 1663-1669. DOI: 10.1016/J.Tetasy.2012.10.021 |
0.366 |
|
| 2012 |
Stingl KA, Weiß KM, Tsogoeva SB. Asymmetric vanadium- and iron-catalyzed oxidations: new mild (R)-modafinil synthesis and formation of epoxides using aqueous H2O2 as a terminal oxidant Tetrahedron. 68: 8493-8501. DOI: 10.1016/J.Tet.2012.07.052 |
0.363 |
|
| 2012 |
Serdyuk OV, Zamfir A, Hampel F, Tsogoeva SB. Combiningin situGenerated Chiral Silicon Lewis Acid and Chiral Brønsted Acid Catalysts for [3+2] Cycloadditions: Cooperative Catalysis as a Convenient Enantioselective Route to Pyrazolidines Advanced Synthesis & Catalysis. 354: 3115-3121. DOI: 10.1002/Adsc.201200293 |
0.389 |
|
| 2011 |
Wei S, Messerer R, Tsogoeva SB. Asymmetric synthesis of β-adrenergic blockers through multistep one-pot transformations involving in situ chiral organocatalyst formation. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 14380-4. PMID 22113987 DOI: 10.1002/Chem.201102931 |
0.383 |
|
| 2011 |
Weiss KM, Wei S, Tsogoeva SB. Novel one-pot process for the synthesis of 1,3-thiazoles via organocatalysed epoxidation of nitro-olefins. Organic & Biomolecular Chemistry. 9: 3457-61. PMID 21431165 DOI: 10.1039/C1Ob05260H |
0.383 |
|
| 2011 |
Weiss KM, Tsogoeva SB. Enantioselective epoxidation of electron-deficient olefins: an organocatalytic approach. Chemical Record (New York, N.Y.). 11: 18-39. PMID 21308970 DOI: 10.1002/Tcr.201000006 |
0.341 |
|
| 2011 |
Tsogoeva S, Zamfir A. Towards a Catalytic Asymmetric Version of the [3+2] Cycloaddition between Hydrazones and Cyclopentadiene Synthesis. 2011: 1988-1992. DOI: 10.1055/S-0030-1260467 |
0.389 |
|
| 2011 |
Tsogoeva S, Freund M. l-Proline-Catalyzed Asymmetric Michael Addition of 2-Oxindoles to Enones: A Convenient Access to Oxindoles with a Quaternary Stereocenter Synlett. 2011: 503-507. DOI: 10.1055/S-0030-1259527 |
0.373 |
|
| 2011 |
Zamfir A, Schenker S, Bauer W, Clark T, Tsogoeva SB. Silicon Lewis Acid Catalyzed [3+2] Cycloaddition Reactions of Hydrazones/Cyclopentadiene: Mild Access to Pyrazolidine Derivatives European Journal of Organic Chemistry. 2011: 3706-3709. DOI: 10.1002/Ejoc.201100206 |
0.442 |
|
| 2011 |
Schenker S, Zamfir A, Freund M, Tsogoeva SB. Developments in Chiral Binaphthyl-Derived Brønsted/Lewis Acids and Hydrogen-Bond-Donor Organocatalysis European Journal of Organic Chemistry. 2011: 2209-2222. DOI: 10.1002/Ejoc.201001538 |
0.353 |
|
| 2010 |
Tsogoeva SB. When chiral product and catalyst are the same: discovery of asymmetric organoautocatalysis. Chemical Communications (Cambridge, England). 46: 7662-9. PMID 20830352 DOI: 10.1039/C0Cc02305A |
0.38 |
|
| 2010 |
Zamfir A, Schenker S, Freund M, Tsogoeva SB. Chiral BINOL-derived phosphoric acids: privileged Brønsted acid organocatalysts for C-C bond formation reactions. Organic & Biomolecular Chemistry. 8: 5262-76. PMID 20820680 DOI: 10.1039/C0Ob00209G |
0.388 |
|
| 2010 |
Tsogoeva SB. Recent progress in the development of synthetic hybrids of natural or unnatural bioactive compounds for medicinal chemistry. Mini Reviews in Medicinal Chemistry. 10: 773-93. PMID 20105118 DOI: 10.2174/138955710791608280 |
0.327 |
|
| 2010 |
Zamfir A, Tsogoeva SB. Asymmetric hydrocyanation of hydrazones catalyzed by in situ formed O-silylated BINOL-phosphate: a convenient access to versatile alpha-hydrazino acids. Organic Letters. 12: 188-91. PMID 19950926 DOI: 10.1021/Ol9025974 |
0.337 |
|
| 2010 |
Mauksch M, Wei S, Freund M, Zamfir A, Tsogoeva SB. Spontaneous mirror symmetry breaking in the aldol reaction and its potential relevance in prebiotic chemistry. Origins of Life and Evolution of the Biosphere : the Journal of the International Society For the Study of the Origin of Life. 40: 79-91. PMID 19911304 DOI: 10.1007/S11084-009-9177-2 |
0.393 |
|
| 2010 |
Tsogoeva S, Wei S, Stingl K, Weiß K. Thieme Chemistry Journal Awardees - Where Are They Now? Bifunctional Organocatalysis with N-Formyl-l-Proline: A Novel Approach to Epoxide Ring Opening and Sulfide Oxidation Synlett. 2010: 707-711. DOI: 10.1055/S-0029-1219363 |
0.337 |
|
| 2010 |
Stingl KA, Tsogoeva SB. Recent advances in sulfoxidation reactions: a metal-free approach Tetrahedron: Asymmetry. 21: 1055-1074. DOI: 10.1016/J.Tetasy.2010.05.020 |
0.384 |
|
| 2009 |
Freund M, Schenker S, Tsogoeva SB. Enantioselective nitro-Michael reactions catalyzed by short peptides on water. Organic & Biomolecular Chemistry. 7: 4279-84. PMID 19795068 DOI: 10.1039/B910249C |
0.367 |
|
| 2009 |
Wei S, Mauksch M, Tsogoeva SB. Autocatalytic enantiomerisation at the crystal surface in deracemisation of scalemic conglomerates. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 10255-62. PMID 19693755 DOI: 10.1002/Chem.200900979 |
0.351 |
|
| 2009 |
Tsogoeva SB, Wei S, Freund M, Mauksch M. Generation of highly enantioenriched crystalline products in reversible asymmetric reactions with racemic or achiral catalysts. Angewandte Chemie (International Ed. in English). 48: 590-4. PMID 19072810 DOI: 10.1002/Anie.200803877 |
0.38 |
|
| 2008 |
Mauksch M, Tsogoeva SB. Spontaneous emergence of homochirality via coherently coupled antagonistic and reversible reaction cycles. Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry. 9: 2359-71. PMID 18942050 DOI: 10.1002/Cphc.200800226 |
0.393 |
|
| 2008 |
Baudequin C, Zamfir A, Tsogoeva SB. Highly enantioselective organocatalytic formation of a quaternary carbon center via chiral Brønsted acid catalyzed self-coupling of enamides. Chemical Communications (Cambridge, England). 4637-9. PMID 18815709 DOI: 10.1039/B804477E |
0.354 |
|
| 2008 |
Yalalov DA, Tsogoeva SB, Shubina TE, Martynova IM, Clark T. Evidence for an enol mechanism in a highly enantioselective Mannich-type reaction catalyzed by primary amine-thiourea. Angewandte Chemie (International Ed. in English). 47: 6624-8. PMID 18646234 DOI: 10.1002/Anie.200800849 |
0.387 |
|
| 2007 |
Mauksch M, Tsogoeva SB, Wei S, Martynova IM. Demonstration of spontaneous chiral symmetry breaking in asymmetric Mannich and Aldol reactions. Chirality. 19: 816-25. PMID 17786910 DOI: 10.1002/Chir.20474 |
0.418 |
|
| 2007 |
Mauksch M, Tsogoeva SB, Martynova IM, Wei S. Evidence of asymmetric autocatalysis in organocatalytic reactions. Angewandte Chemie (International Ed. in English). 46: 393-6. PMID 17146824 DOI: 10.1002/Anie.200603517 |
0.369 |
|
| 2007 |
Wei S, Yalalov DA, Tsogoeva SB, Schmatz S. New highly enantioselective thiourea-based bifunctional organocatalysts for nitro-Michael addition reactions Catalysis Today. 121: 151-157. DOI: 10.1016/J.Cattod.2006.11.018 |
0.39 |
|
| 2007 |
Baudequin C, Chaturvedi D, Tsogoeva SB. Organocatalysis with chiral formamides: Asymmetric allylation and reduction of imines European Journal of Organic Chemistry. 2623-2629. DOI: 10.1002/Ejoc.200700058 |
0.424 |
|
| 2007 |
Tsogoeva SB. Recent Advances in Asymmetric Organocatalytic 1,4-Conjugate Additions Cheminform. 38. DOI: 10.1002/Ejoc.200600653 |
0.424 |
|
| 2006 |
Jagtap SB, Tsogoeva SB. First enantioselective organocatalytic allylation of simple aldimines with allyltrichlorosilane. Chemical Communications (Cambridge, England). 4747-9. PMID 17109057 DOI: 10.1039/B611823B |
0.378 |
|
| 2006 |
Tsogoeva SB, Wei S. Highly enantioselective addition of ketones to nitroolefins catalyzed by new thiourea-amine bifunctional organocatalysts. Chemical Communications (Cambridge, England). 1451-3. PMID 16550297 DOI: 10.1039/B517937H |
0.403 |
|
| 2006 |
Tsogoeva SB. Asymmetric Organocatalysis: From Biomimetic Concepts to Applications in Asymmetric Synthesis Synthesis. 2006: 736-736. DOI: 10.1055/S-2006-932678 |
0.34 |
|
| 2006 |
Tsogoeva SB, Jagtap SB, Ardemasova ZA. 4-trans-Amino-Proline Based Di- and Tetrapeptides as Organic Catalysts for Asymmetric C—C Bond Formation Reactions. Cheminform. 37. DOI: 10.1016/J.Tetasy.2006.03.012 |
0.436 |
|
| 2006 |
Tsogoeva SB, Yalalov DA, Hateley MJ, Weckbecker C, Huthmacher K. Asymmetric Organocatalysis with Novel Chiral Thiourea Derivatives: Bifunctional Catalysts for the Strecker and Nitro-Michael Reactions. Cheminform. 37. DOI: 10.1002/Ejoc.200500420 |
0.437 |
|
| 2006 |
Yalalov D, Tsogoeva S, Schmatz S. Chiral Thiourea-Based Bifunctional Organocatalysts in the Asymmetric Nitro-Michael Addition: A Joint Experimental-Theoretical Study Advanced Synthesis & Catalysis. 348: 826-832. DOI: 10.1002/Adsc.200505443 |
0.347 |
|
| 2005 |
Tsogoeva SB, Hateley MJ, Yalalov DA, Meindl K, Weckbecker C, Huthmacher K. Thiourea-based non-nucleoside inhibitors of HIV reverse transcriptase as bifunctional organocatalysts in the asymmetric Strecker synthesis. Bioorganic & Medicinal Chemistry. 13: 5680-5. PMID 15964195 DOI: 10.1016/J.Bmc.2005.05.014 |
0.331 |
|
| 2005 |
Tsogoeva SB, Wei S. (S)-Histidine-Based Dipeptides as Organic Catalysts for Direct Asymmetric Aldol Reactions. Cheminform. 36. DOI: 10.1016/J.Tetasy.2005.04.027 |
0.42 |
|
| 2005 |
Tsogoeva SB, Yalalov DA, Hateley MJ, Weckbecker C, Huthmacher K. Asymmetric Organocatalysis with Novel Chiral Thiourea Derivatives: Bifunctional Catalysts for the Strecker and Nitro-Michael Reactions European Journal of Organic Chemistry. 2005: 4995-5000. DOI: 10.1002/EJOC.200500420 |
0.307 |
|
| 2004 |
Tsogoeva S, Jagtap S. Dual Catalyst Control in the Chiral Diamine-Dipeptide-Catalyzed Asymmetric Michael Addition Synlett. 2004: 2624-2626. DOI: 10.1055/S-2004-834830 |
0.375 |
|
| 2004 |
Tsogoeva S, Jagtap S, Ardemasova Z, Kalikhevich V. Trends in Asymmetric Michael Reactions Catalysed by Tripeptides in Combination with an Achiral Additive in Different Solvents European Journal of Organic Chemistry. 2004: 4014-4019. DOI: 10.1002/Ejoc.200400243 |
0.393 |
|
| 2003 |
Tsogoeva S, Dürner G, Bolte M, Göbel M. A C2-Chiral Bis(amidinium) Catalyst for a Diels−Alder Reaction Constituting the Key Step of the Quinkert−Dane Estrone Synthesis European Journal of Organic Chemistry. 2003: 1661-1664. DOI: 10.1002/Ejoc.200200635 |
0.335 |
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| 2002 |
Tsogoeva SB, Wöltinger J, Jost C, Reichert D, Kühnle A, Krimmer H, Drauz K. Juliá-Colonna Asymmetric Epoxidation in a Continuously Operated Chemzyme Membrane Reactor Synlett. 2002: 0707-0710. DOI: 10.1055/S-2002-25352 |
0.314 |
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