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2011

55. Asymmetric Synthesis of beta-Adrenergic Blockers via Multi-step One-Pot Transformations involving in situ Chiral Organocatalyst Formation. S.-W. Wei, R. Messerer, S. B. Tsogoeva. Chem. Eur. J. 2011, 17, 14380-14384. (Highlighted in Noteworthy Chemistry, weekly feature by ACS, January 9, 2012).

54. Assessment of Popular DFT and Semiempirical Molecular Orbital Techniques for Calculating Relative Transition State Energies and Kinetic Product Distributions in Enantioselective Organocatalytic Reactions. S. Schenker, C. Schneider, S. B. Tsogoeva, T. Clark, J. Chem. Theor. Comput., 2011, 7, 3586-3595.

53. L-Proline Catalyzed Asymmetric Michael Addition of 2-Oxindoles to Enones: A Convenient Access to Oxindoles with a Quaternary Stereocenter. M. H. Freund, S. B. Tsogoeva. Synlett: Cluster (Invited Article), 2011, 503-507.

52. Enantioselective Epoxidation of Electron-Deficient Olefins: An Organocatalytic Approach. K. M. Weiß and S. B. Tsogoeva. The Chemical Record (Invited Perspective. Dedicated to Prof. Andreas Hirsch on the occasion of his 50th birthday), 2011, 11, 18-39. (Among Hottest articles in Organic Chemistry. Most accessed 3/2011-2/2012).

51. Binaphthyl-Derived Mono-, Bi- and Multi-functional Lewis and Brønsted Base Organocatalysts: A New Vista for Asymmetric Synthesis. M. Freund, S. Schenker, A. Zamfir and S. B. Tsogoeva. Curr. Org. Chem. (Invited Review in a Special Issue “Fundamentals in Organocatalysis. Past, Present and Future”), 2011, 15, 2282-2310.

50. "Life’s Single Chirality: Origin of Symmetry Breaking in Biomolecules." M. Mauksch and S. B. Tsogoeva. (Book Chapter in "Biomimetic Organic Synthesis," E. Poupon / B. Nay (Eds.), WILEY-VCH, 2011, Vol. 2, 823-846.

49. Silicon Lewis Acid Catalyzed [3+2] Cycloaddition Reactions of Hydrazones/Cyclopentadiene: Novel Mild Access to Pyrazolidine Derivatives. A. Zamfir, S. Schenker, W. Bauer, T. Clark and S. B. Tsogoeva. Eur. J. Org. Chem., (Invited Communication in a Special Issue: Women in Chemistry, Profiles), 2011, 3706-3709.

48. Novel one-pot process for the synthesis of 1,3-thiazoles via organocatalysed epoxidation of nitro-olefins. K. M. Weiß, S.-W. Wei, S. B. Tsogoeva. Org. Biomol. Chem. 2011, 9, 3457-3461 (Highlighted in SYNFACTS, 2011, 6, 595).

47. Developments in Chiral Binaphthyl-Derived Brønsted / Lewis Acids and Hydrogen-Bond Donor Organocatalysis. S. Schenker, A. Zamfir, M. Freund, S. B. Tsogoeva. Eur. J. Org. Chem., (Invited Microreview), 2011, 2209-2222 (Most accessed 2/2011-1/2012).

46. "Peptides for asymmetric catalysis." M. Freund and S. B. Tsogoeva. (Book Chapter in "Catalytic Methods in Asymmetric Synthesis: Advanced Materials, Techniques, and Applications," M. Gruttadauria / F. Giacalone (Eds.), John WILEY & Sons, 2011, Chapter 13, 529-578.

45. Towards a Catalytic Asymmetric Version of the [3+2] Cycloaddition Between Hydrazones and Cyclopentadiene. A. Zamfir, S. B. Tsogoeva. Synthesis (Invited Article), 2011, 1988-1992.

2010

44. Asymmetric Hydrocyanation of Hydrazones Catalyzed by in situ Formed O-silylated BINOL-Phosphate: A Convenient Access to Versatile α-Hydrazino Acids. A. Zamfir, S. B. Tsogoeva. Org. Lett. (paper dedicated to Prof. Rolf W. Saalfrank on the occasion of his 70th birthday), 2010, 12, 188-191.

43. When chiral product and catalyst are the same: Discovery of asymmetric organoautocatalysis. S. B. Tsogoeva. Chem. Commun. (Invited Feature Article) 2010, 46, 7662-7669 (Highlighted in ChemInform, 2011, Vol. 42, Issue 6).

42. Bifunctional Organocatalysis with N-Formyl-L-Proline: A Novel Approach to Epoxide Ring Opening and Sulfide Oxidation. S.-W. Wei, K. A. Stingl, K. M. Weiß, S. B. Tsogoeva. Synlett (Invited Article), 2010, 707-711.

41. A Novel Five-coordinate Mn Complex with a Redox-active SNNNS Ligand System. K. Dürr, D. A. Yalalov, F. W. Heinemann, S. B. Tsogoeva, I. Ivanovic-Burmazovic. Z. Naturforsch. B (paper dedicated to Prof. Rolf W. Saalfrank on the occasion of his 70th birthday), 2010, 65b, 258-262.

40. Spontaneous Mirror Symmetry Breaking in the Aldol Reaction and its Potential Relevance in Prebiotic Chemistry. M. Mauksch, S.-W. Wei, M. Freund, A. Zamfir, S. B. Tsogoeva. Origins of Life and Evolution of Biospheres, 2010, 40, 79-91.

39. Recent Progress in the Development of Synthetic Hybrids of Natural or Unnatural Bioactive Compounds for Medicinal Chemistry. S. B. Tsogoeva. Mini Rev. Med. Chem., (Invited Review) 2010, 10(9), 773-793.

38. Cytotoxicity of Artesunic Acid Homo- and Heterodimer Molecules towards Sensitive and Multidrug-Resistant CCRF-CEM Leukemia Cells. C. Horwedel, S. B. Tsogoeva, S.-W. Wei, T. Efferth. J. Med. Chem. 2010, 53, 4842–4848.

37. Recent Advances in Sulfoxidation Reactions: A Metal-free Approach. K. A. Stingl, S. B. Tsogoeva. Review in Tetrahedron: Asymmetry (special issue to celebrate the 80th birthday of Professor Henri Kagan), 2010, 21, 1055-1074.

36. Demonstration of “Möbius” Aromaticity in Planar Metallacycles. M. Mauksch, S. B. Tsogoeva. Chem. Eur. J. (paper dedicated to Prof. Paul von Ragué Schleyer on the occasion of his 80th birthday), 2010, 16, 7843-7851.

35. Organoautocatalysis: Challenges for Experiment and Theory. S. B. Tsogoeva. Review in Journal of Systems Chemistry, 2010, 1:8.

34. Chiral BINOL-derived phosphoric acids: Privileged Brønsted acid organocatalysts for C-C bond formation reactions. A. Zamfir, S. Schenker, M. Freund and S. B. Tsogoeva. Org. Biomol. Chem. (Invited Perspective), 2010, 8, 5262-5276.

2009

33. Generation of Highly Enantioenriched Crystalline Products in Reversible Asymmetric Reactions with Racemic or Achiral Catalysts. S. B. Tsogoeva, S.-W. Wei, M. Freund, M. Mauksch. Angew. Chem. Int. Ed. 2009, 48, 590-594; Angew. Chem. 2009, 121, 598-602 (see also: Chemical & Engineering News, March 23, 2009/ V. 87, PP. 38-41).

32. A Preferred Disrotatory 4n Electron Möbius Aromatic Transition State for a Thermal Electrocyclic Reaction. M. Mauksch, S. B. Tsogoeva. Angew. Chem. Int. Ed. 2009, 48, 2959-2963; Angew. Chem. 2009, 121, 3003-3007.

31. Autocatalytic Enantiomerization at the Crystal Surface in Derazemisation of Scalemic Conglomerates. S.-W. Wei, M. Mauksch, S. B. Tsogoeva. Chem. Eur. J. 2009, 15, 10255-10262.

30. Enantioselective nitro-Michael reactions catalyzed by short peptides on water. M. Freund, S. Schenker, S. B. Tsogoeva. Org. Biomol. Chem. 2009, 7, 4279-4284.

2008

29. Evidence for an Enol Mechanism in a Highly Enantioselective Mannich-type Reaction Catalyzed by Primary Amine-Thiourea. D. A. Yalalov, S. B. Tsogoeva, T. E. Shubina, I. M. Martynova, T. Clark. Angew. Chem. Int. Ed. 2008, 47, 6624-6628; Angew. Chem. 2008, 120, 6726-6730. (Highlighted in ChemInform, 2008, Vol. 39, Issue 50).

28. Spontaneous Emergence of Homochirality via Coherently Coupled Antagonistic and Reversible Reaction Cycles. M. Mauksch, S. B. Tsogoeva. ChemPhysChem. 2008, 9, 2359-2371. (Highlighted in Pharmacy Research Today , 2008, Volume 4, Issue 11).

27. Highly enantioselective organocatalytic formation of quaternary carbon center via chiral Brønsted acid catalyzed self-coupling of enamides. C. Baudequin, A. Zamfir, S. B. Tsogoeva. Chem. Commun. 2008, 4637-4639.

26. Neutral Möbius Aromatics: Derivatives of the Pyrrol Congener Aza[11]annulene as promising Synthetic Targets. M. Mauksch, S. B. Tsogoeva. Eur. J. Org. Chem. 2008, 5755-5763.

2007

25. Recent Advances in Asymmetric Organocatalytic 1,4-Conjugate Additions. S. B. Tsogoeva. Invited Microreview in Eur. J. Org. Chem. 2007, 1701-1716. Most-cited article of all articles published in 2007 in the subject category “Chemistry, Organic”, 500 citations (ISI Web of Science, 30.01.2012), Highlighted in ChemInform, 2007, Vol. 38, Issue 27; Highlighted in Chemistry Views, 2012.

24. Evidence of Asymmetric Autocatalysis in Organocatalytic Reactions. M. Mauksch, S. B. Tsogoeva, I. M. Martynova, S.-W. Wei. Angew. Chem. Int. Ed. 2007, 46, 393-396; Angew. Chem. 2007, 119, 397-400. (Promoted to “Hot Paper” by decision of the Editorial Board; Highlighted in SYNFORM Issue 2007/01; Synlett, Issue 8, 2007; and in Organic Process Research & Development, 2007 , Vol. 11, No. 3, p. 301).

23. New highly enantioselective thiourea-based bifunctional organocatalysts for nitro-Michael addition reactions. S.-W. Wei, D. A. Yalalov, S. B. Tsogoeva, S. Schmatz. Catalysis Today. 2007, 121, 151-157.

22. Organocatalysis with chiral formamides: Asymmetric Allylation and Reduction of Imines. C. Baudequin, D. Chaturvedi, S. B. Tsogoeva. Eur. J. Org. Chem. 2007, 2623-2629. (Most accessed 03/2007-02/2008; Highlighted in ChemInform, 2007, Vol. 38, Issue 38).

21. Demonstration of Spontaneous Chiral Symmetry Breaking in Asymmetric Mannich and Aldol Reactions. M. Mauksch, S. B. Tsogoeva, S.-W. Wei, I. M. Martynova. Chirality, 2007, 19, 816-825.

2006

20. First enantioselective organocatalytic allylation of simple aldimines with allyltrichlorosilane. S. B. Jagtap, S. B. Tsogoeva. Chem. Commun. 2006, 4747. (Highlighted in ChemInform, 2007, Vol. 38, Issue 13).

19. Highly enantioselective addition of ketones to nitroolefins catalyzed by new thiourea-amine bifunctional organocatalysts. S. B. Tsogoeva, S.-W. Wei. Chem. Commun. 2006, 1451. (Highlighted in ChemInform, 2006, Vol. 37, Issue 32).

18. 4-trans-Amino-proline based di- and tetrapeptides as organic catalysts for asymmetric C-C bond formation reactions. S. B. Tsogoeva, S. B. Jagtap, Z. A. Ardemasova. Tetrahedron: Asymmetry. 2006, 17, 989. (Among TOP25 Articles in 2006; Highlighted in ChemInform, 2006, Vol. 37, Issue 37).

17. Chiral Thiourea-Based Bifunctional Organocatalysts in the Asymmetric Nitro-Michael Addition: A Joint Experimental-Theoretical Study. D. A. Yalalov, S. B. Tsogoeva, S. Schmatz. Advanced Synthesis & Catalysis. 2006, 348, 826.

16. “Asymmetric Organocatalysis. From Biomimetic Concepts to Applications in Asymmetric Synthesis”(Book Review) (by A. Berkessel and H. Gröger. Wiley-VCH, Weinheim 2005). S. B. Tsogoeva. Synthesis. 2006, 736.

2005

15. Asymmetric Organocatalysis with Novel Chiral Thiourea Derivatives: Bifunctional Catalysts for the Strecker and nitro-Michael Reactions. S. B. Tsogoeva, D. A. Yalalov, M. J. Hateley, C. Weckbecker, K. Huthmacher. Eur. J. Org. Chem. 2005, 4995. (Among TOP10 most accessed articles in 10/2005; among most accessed articles in 2006; Highlighted in ChemInform, 2006, Vol. 37, Issue 12).

14. “Transition Metals for Organic Synthesis. Building Blocks and Fine Chemicals”(Book Review) (M. Beller and C. Bolm (Ed.). Wiley-VCH, Weinheim 2004). S. B. Tsogoeva. Angew. Chem. Int. Ed. 2005, 44, 3337; Angew. Chem. 2005, 117, 3401.

13. Thiourea-based Non-nucleoside Inhibitors of HIV Reverse Transcriptase as Bifunctional Organocatalysts in the Asymmetric Strecker Synthesis. S. B. Tsogoeva, M. J. Hateley, D. A. Yalalov, K. Meindl, C. Weckbecker, K. Huthmacher. Bioorg. Med. Chem. 2005, 13, 5680.

12. (S)-Histidine-based Dipeptides as Organic Catalysts for Direct Asymmetric Aldol Reactions. S. B. Tsogoeva, S.-W. Wei. Tetrahedron: Asymmetry, 2005, 16, 1947. (Has been recognised with the "Most Cited Paper 2005-2008 Award"; Highlighted in ChemInform, 2005, Vol. 36, Issue 43).

11. Short Peptides and Peptide-Like Enzyme Mimics - Efficient Organic Catalysts in Asymmetric Synthesis. S. B. Tsogoeva. Invited Review in: Letters in Organic Chemistry, 2005, 2, 208. (Highlighted in ChemInform, 2006, Vol. 37, Issue 6).

2004

10. Dual Catalyst Control in the chiral Diamine-Dipeptide-Catalyzed Asymmetric Michael Addition. S. B. Tsogoeva, S. B. Jagtap. Synlett. 2004, 2624.

9. Trends in Asymmetric Michael Reactions Catalysed by Tripeptides in Combination with an Achiral Additive in Different Solvents. S. B. Tsogoeva, S. B. Jagtap, Z. A. Ardemasova, V. N. Kalikhevich. Eur. J. Org. Chem. 2004, 4014. (Highlighted in ChemInform, 2005, Vol. 36, Issue 4).

2002-2003

8. C2-Chiral Bis(Amidinium)-Catalyst for a Diels-Alder Reaction Constituting the Key Step of the Quinkert-Dane Estrone Synthesis. S. B. Tsogoeva, G. Dürner, M. Bolte, M. W. Göbel. Eur. J. Org. Chem. 2003, 1661.

7. Juliá-Colonna Asymmetric Epoxidation in a Continuously Operated Chemzyme Membrane Reactor. S. B. Tsogoeva, J. Wöltinger, C. Jost, D. Reichert, A. Kühnle, H.-P. Krimmer, K.-H. Drauz. Synlett. 2002, 707.

6. A Study of the Binding of Estradiol and 8-Isoestradiol to the Estrogen a -Receptor by Molecular Modeling. A. G. Shavva, K. V. Vlasova, S. B. Tsogoeva, M. S. Egorov, P. P. Yakutseni. Russian Journal of Bioorganic Chemistry. 2002, 28, 209.

1998-2001

5. Molecular Structures of Some 8-Isoanalogues of Steroid Estrogens. G. L. Starova, I. I. Eliseev, Sh. N. Abasalimov, S. B. Tsogoeva, A.G. Shavva. Crystallography Reports. 2001, 46, 65.

4. A Study of the Molecular Structure of 3-Methoxy-7a-Methyl-8,14-Iso-1,3,5(10)-Estratrien-17b-ol Acetate by X-ray Diffraction and Molecular Modeling Methods. G. L. Starova, S. B. Tsogoeva, I. I. Eliseev, A. G. Shavva. Crystallography Reports. 1999, 44, 450.

3. Molecular structure of (±)-3-methoxy-6-oxa-8-iso-1,3,5(10)-estratrien-17b-ol acetate. G. L. Starova, S. B. Tsogoeva, A. G. Shavva. Crystallography Reports. 1998, 43, 31.

2. Ionic hydrogenation of 6-oxaestra-1,3,5(10),8,14-pentaenes. S. B. Tsogoeva, S. I., Selivanov, A. G. Shavva. Russian Journal of Organic Chemistry. 1998, 34, 1297.

1. NMR study of (±)-17 b -acetoxy-3-methoxy-6-oxa-8-isoestra-1,3,5(10)-triene. S. I. Selivanov, S. B. Tsogoeva, A. G. Shavva. Russian Journal of Organic Chemistry. 1998, 34, 1292.