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Arbeitskreis Kalesse

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Schriftenverzeichnis

  1. Highly Stereoselective Aldol Reactions in the Total Syntheses of Complex Natural Products, T. Brodmann, M. Lorenz, R. Schäckel, S. Simsek, M. Kalesse, Synlett, 2009, 2, 174.
  2. Synthesis of the C10-C32 Core Structure of Spirangien A, M. Lorenz, M. Kalesse, Org. Lett., 2008, 10, 4371.
  3. Interaction between importin 13 and myopodin suggests a nuclear import pathway for myopodin, J. Liang, G. Ke, W. You, Z. Peng, J. Lan, M. Kalesse, A. M. Tartakoff, F Kaplann, T. Tao, Mol. Cell. Biochem., 2008, 307, 93-100.
  4. The Total Synthesis of (+)-Tedanolide, a Macrocyclic Polyketide From Marine Sponge Tedania Ignis, G. Ehrlich, J. Hassfeld, U. Eggert, M. Kalesse, Chemistry - Europ. Journal, 2008, in press .
  5. The First Total Synthesis of Chlorotonil, N. Rahn, M. Kalesse, Angew. Chem., 2008, 120, 607-609.
  6. Oxazaborolidinone Promoted Vinylogous Mukaiyama Aldol Reactions, S. Simsek, M. Horzella, M. Kalesse, Org. Lett., 2007, 9, 5637-5639.
  7. Synthesis of the C15-C35 Segment of Chivosazole, D. Janssen, M. Kalesse, Synlett, 2007, 2667-2670.
  8. Synthesis of the C23-C32 Fragment of Spirangien, M. Lorenz, M. Kalesse, Tetrahedron Lett., 2007, 48, 2905-2907.
  9. Chivosazole A – Elucidation of the full absolute and relative configuration, D. Janssen, D. Albert, R. Jansen, R. Müller, M. Kalesse, Angew. Chem., 2007, 119, 4985-4988.
  10. The Total Synthesis of (+)-Tedanolide, G. Ehrlich, J. Hassfeld, U. Eggert, M. Kalesse, J. Am. Chem. Soc., 2006, 128, 14038-14039.
  11. TAR-RNA recognition by a novel aminoglycoside analogue, D. Ragunathan, V. M. Sanchez-Pedregal, J. Junker, M. Kalesse, A. Kirschning, T. Carlomagno, Nucl. Acid. Res., 2006, 34, 3599-3608.
  12. Asymmetric Vinylogous Mukaiyama Aldol Reaction, M. Kalesse, J. Hassfeld, Asymmetric Synthesis – The Essentials, (eds. M. Christmann, S. Bräse) Wiley-VCH Verlag, 2006, 100-105.
  13. Tandem Intramolecular Michael-Aldol Reaction as a Tool for the Construction of the C-Ring of Hexacyclinic Acid, A. Stelmakh, T. Stellfeld, M. Kalesse, Org. Lett., 2006, 3485-3488.
  14. Synthesis of a Northern Hemisphere of Amphidinolide H2, F. Liesener, U. Jannsen, M. Kalesse, Synthesis, 2006, 2590-2602.
  15. Synthesis of the C19-C26 Segment of Amphidinolide, F. Liesener, M. Kalesse, Synlett, 2005, 2236-2238.
  16. A One-Pot Non-Aldol-Aldol Vinylogous Mukaiyama Aldol Tandem Sequence for the Rapid Construction of Polyketide Frameworks, N. Rahn, M. Kalesse, Synlett, 2005, 863-865.
  17. Synthesis of the C13-C23 Segment of Tedanolide, G. Ehrlich, M. Kalesse, Synlett, 2005, 655-657.
  18. Synthesis of the C1-C17 Macrolactone of Tedanolide, M. Kalesse, J. Hassfeld, U. Eggert, Synthesis, 2005, 1183-1199.
  19. Synthesis of the A,B,C-Ring System of Hexacyclinic Acid, T. Stellfeld, U. Bhatt, M. Kalesse, Org. Lett., 2004, 6, 3889-3892.
  20. Synthesis of extended spacer-linked neooligodeoxysaccharides by metathesisolefination and evaluation of their RNA-binding properties, A. Kirschning, M. Lindner, M. Kalesse, Tetrahedron, 2004, 60, 3505-3521.
  21. Ratjadone is a potent inhibitor of coronary smooth muscle cell proliferation and induces cell differentiation, B. Witzenbichler, M. Kalesse, S. Knüppel, H. P. Schultheiss, Circulation 2004, 60, 3505-3521.
  22. Ratjadone is a potent inhibitor of vascular smooth muscle cell proliferation, B. Witzenbichler, M. Kalesse, S. Knüppel, H. P. Schultheiss, European Heart Journal, 2003, 24, 333.
  23. Multi parameter in vitro testing of ratjadone using flow cytometry, A. Burzlaff, M. Kalesse, C. Kasper, T. Scheper, Appl. Microbiol. Bitechnol., 2003, 62, 174-179.
  24. The Total Synthesis of (-)-Callystatin A, M. Kalesse, M. Quitschalle, C.P. Khandavalli, Chem. Eur. J., 2003, 9, No. 5, 1129-1136.
  25. Synthesis of the C1-C11 Segment of Tedanolide via Vinylogous Mukaiyama Aldol Reaction, J. Hassfeld, M. Kalesse, Synlett, 2002, 2007-2010.
  26. Advances in the vinylogous Mukaiyama aldol reaction and its application to the synthesis of the C1-C7 subunit of oleandolide, J. Hassfeld, M. Kalesse, Tetrahedron Lett., 2002, 5093-5095.
  27. The Chemistry and Biology of the Leptomycin family, M. Kalesse, M. Christmann, Synthesis (review), 2002, 981-1003.
  28. Rapid access to polyketide scaffolds via vinylogous Mukaiyama aldol reactions, J. Hassfeld, M. Christmann and M. Kalesse, Org. Lett., 2001, 3561-3564.
  29. The Synthesis of (-)-Callystatin A, M. Kalesse, M. Quitschalle, C.P. Khandavalli, A. Saeed, Org. Lett., 2001, 3107-3109.
  30. The Biology and Chemsitry of Ratjadone, M. Christmann, U. Bhatt, M. Quitschalle, Winfried Beil, Arne Burzlaff, Cornelia Kasper, L.-O. Haustedt, E. Hofer, T. Scheper, M. Kalesse, ChemBioChem, 2001, 709-714.
  31. Ratjadon-Derivate zum Hemmen des Zellwachstums, Patent angemeldet; (DE, Nr.: 100 47 794.1) U. Bhatt, C. P. Khandavalli, M. Christmann, M. Quitschalle, T. Scheper, W. Beil, A. Burzlaff, C. Kasper, E. Claus, M. Kalesse, 2001.
  32. The Total Synthesis of (+)-Ratjadone, M. Christmann, U. Bhatt, M. Quitschalle, E. Claus, M. Kalesse, J. Org. Chem., 2001, 1885-1893.
  33. Vinylogous Mukaiyama Aldol Reactions with Triarylboranes, M. Christmann, M. Kalesse, Tetrahedron Lett., 2001, 42, 1269-1271.
  34. Synthesis of Unsaturated Lactone Moieties by Asymmetric Hetero Diels-Alder Reactions with Binaphthol-Titanium Complexes, M. Quitschalle, M. Christmann, U. Bhatt, M. Kalesse, Tetrahedron Lett., 2001, 42, 1263-1265.
  35. Uridin-spezifische Ribonuklease, Patent angemeldet; (DE, Nr.: 100 47 794) K. Michaelis, M. Kalesse.
  36. Selective Cleavage of Unpaired Uridines with a Tyrosine-Cyclen Conjugate, K. Michaelis, M. Kalesse, ChemBioChem., 2001, 1, 79-83.
  37. Total Synthesis of (+)-Ratjadone, M. Christmann, U. Bhatt, M. Quitschalle, E. Claus, M. Kalesse, Angew. Chem., 2000, 112, 4535-4538; Angew. Chem. Int. Ed., 2000, 39, 4364-4366.
  38. The Chemistry and Biology of Discodermolide, M. Kalesse, Highlight, ChemBioChem., 2000, 1, 171-175.
  39. Improved Synthesis of the Northern Hemisphere of Epothilone A by a Sharpless Asymmetric Dihydroxylation, M. Quitschalle and M. Kalesse, Tetrahedron Lett., 1999, 40, 7765-7768.
  40. The Synthesis of the C15-C24 Segment of Ratjadone, M. Christmann, M. Kalesse, Tetrahedron Lett., 1999, 40, 7201-7204.
  41. The Synthesis of Epothilone A, M. Kalesse, M. Quitschalle, E. Claus, K. Gerlach, A. Pahl, H.H. Meyer, Eur. J. Org. Chem., 1999, 2817-2823.
  42. Synthesis of the C6-C16 Polyene Fragment of Ratjadone, a Potent Cytotoxic Metabolite from Sorangium Cellulosum, E. Claus, M. Kalesse, Tetrahedron Lett., 1999, 40, 4157-4160.
  43. Synthesis of the Northern Hemisphere of Epothilone A by a Ten-Membered Ring Closing Metathesis Reaction, K. Gerlach, M. Quitschalle, M. Kalesse, Tetrahedron Lett., 1999, 40, 3553-3556.
  44. Selective Cleavage of the HIV-1 TAR RNA with a Peptide-Cyclen Conjugate, K. Michaelis, M. Kalesse, Angew. Chem., 1999, 111, 2382-2385; Angew. Chem. Int. Ed., 1999, 38, 2243-2245.
  45. Synthesis of Steroid Derived RNAse Active Site Model Systems: Modification of the C17 Pendant Imidazole and Substitution of the Guanidinium Groups, T. Oost, M. Kalesse, Polish. J. Chem., 1999, 73, 89-99.
  46. Synthesis of the C7–C17 Segment of Epothilones by a 10-membered Ring Closing Metathesis Reaction, K. Gerlach, M. Quitschalle, M. Kalesse, Synlett, 1998, 1109-1110.
  47. Structural Features for the Promotion of Optimal Stacking in the Solid State, M. Kalesse, R. Wartchow, Tetrahedron, 1998, 54, 8015-8024.
  48. Synthesis of RNAse Active Site Model Systems Using a Steroid Template, T. Oost, M. Kalesse, Tetrahedron, 1997, 53, 8421-8438.
  49. Bis(guanidinium) Receptors as Ribonuclease Active-Site Model Systems: Structural Changes and Solvent Effects, T. Oost, A. Filippazzi, M. Kalesse, Liebigs Ann./Recueil, 1997, 1005-1011.
  50. Epothilone-Synthesebausteine II – Prenylderivate (DE, Nr.: 197 13 970 A1) M. Kalesse, L. Wessjohann.
  51. Synthesis of the C1-C9 Segment of Epothilons, E. Claus, A. Pahl, P.G. Jones, H.H. Meyer, M. Kalesse, Tetrahedron Lett., 1997, 38, 1359-1362.
  52. Generation of Thiazoles by Column Dehydrogenation of Thiazolidines with MnO2, S. Mensching, M. Kalesse, J. prakt. Chem., 1997, 339, 96-97.
  53. Remarkable Hydrolysis of Phosphodiester by Neutral Lanthanide(III) DO3A Complexes, M. Kalesse, A. Loos, Bioorganic & Medicinal Chemistry Letters, 1996, 6, 2063-2068.
  54. Transesterification of Phosphodiester by a Zinc-Containing Cyclen Derivative: Identification of the Active Species, M. Kalesse, A. Loos, Liebigs Ann., 1996, 935-939.
  55. Enantioselective Synthesis of the C1-C9 Segment of Bryostatin by Kinetic Resolution of Racemic β-Keto Esters, M. Kalesse, M. Eh, Tetrahedron Lett., 1996, 37, 1767-1770.
  56. Remarkable Kinetic Resolution of Chiral β-keto Esters by Baker’s Yeast Reduction, M. Eh, M. Kalesse, Synlett, 1995, 837-838.
  57. An Efficient Synthesis of Radicinin Analogues, M. Eh, D. Schomburg, K. Schicht, M. Kalesse, Tetrahedron, 1995, 51, 8983-8992.
  58. Diastereoselective Double Michael Addition of Vinylogous Esters and Thexyldimethylsilyl Trifate-induced Cyclizations, D. Schinzer, M. Kalesse, Tetrahedron Lett., 1991, 36, 4691.
  59. Silica Gel-catalyzed Cyclization of Enones and Double Michael Additions of Vinylogous Amides: Efficient Synthesis of Bicyclo[2.2.2]octanones and Bicyclo-Hydrocarbazoles, D. Schinzer, M. Kalesse, Synlett, 1989, 34.
  60. Silica Gel-catalyzed Cyclization of Mixed Ketene Acetals, D. Schinzer, M. Kalesse, J. Kabbara, Tetrahedron Lett., 1989, 41, 5241.

 

Book Chapters/Conference Proceedings/Other

  1. Science of Synthesis; 25.1.6 „Synthesis of Aldehydes by Protonation“, Band 25 ("Aldehydes"), M. Kalesse, 2007 in press.
  2. Science of Synthesis; 25.1.5 „Synthesis of Aldehydes by the Overall Elimination of HX from Compounds R2CX-CHR-Y“, Band 25 ("Aldehydes") M. Kalesse, 2007, in press.
  3. Asymmetric Total Synthesis of Complex Marine Natural Products, J. Hassfeld, T. Stellfeld, M. Kalesse, M. Christmann, Adv. Biochem. Engin. Biotechnol., 2005, 97, 133.
  4. Vinylogous Aldol Reactions and their Applications in the Syntheses of Natural Products M. Kalesse: Natural Product Synthesis II, Targets, Methods, Concepts Reihe: Topics in Current Chemistry, Band 244, Mulzer, Johann H. (Hrsg.) 2004, 224, 43-76; ISBN: 3-540-21124-1.
  5. Chemie im Computer – zwischen Form und Funktion, M. Kalesse, E. Winterfeldt, L.-O. Haustedt, S. Röper, Uni-Magazin, Universität Hannover, 2002, 1/2, 42-48.
  6. RNase Active Site Model Systems, M. Kalesse, T. Oost, New Perspectives in Bioorganic Chemistry (eds. U. Diedrichsen, B. Westermann et al.) Wiley-VCH Verlag GmbH, 1999, 272-280.
  7. Organic & Bio-organic Mechanism, M. Kalesse, Buchbesprechung, Angew. Chem., 1998, 110, 545-546.
  8. The Race for Epothilones, M. Kalesse, Eur. Chem. Cron., 1997, 2, 7-11.
  9. Bioorganische Chemie M. Kalesse, T. Wirth, Kongressbericht, Nachr. Chem. Techn. Lab., 1996, 44, 1178-1181.
  10. Auf dem Weg zu synthetischen Ribonucleasen, M. Kalesse, A. Loos, T. Oost, GIT Fachzeitschrift für das Laboratorium, 1996, 40, 886-889.
  11. Amberlyst 15 as a Catalyst in Synthetic Organic Chemistry, M. Kalesse, Acros Organics Acta, 1995, 1, 67-68.
  12. Hydrozirconation with Schwartz’s Reagent, M. Kalesse, Acros Organics Acta, 1995, 1, 29-31.
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Verantwortlich: K. Struckmeier


aktualisiert 29.01.2009