Publikationen 2002
Publikationen 2003
Publikationen 2004
Publikationen 2005



319 L.F. Tietze, K. Kahle, T. Raschke Efficient Synthesis of Tetrasubstituted Alkenes by Allylsilane-Terminated Domino-Heck Double Cyclisation. Chem. Eur. J. 2002, 8, 401-407.
320 L.F. Tietze, U. Griesbach, U. Bothe, H. Nakamura, Y. Yamomoto Novel Carboranes with a DNA Binding Unit for the Treatment of Cancer by Boron Neutron Capture Therapy. ChemBioChem. 2002, 3, 219-225.
321 L.F. Tietze, T. Feuerstein, A.Fecher, F. Haunert, O. Panknin, U. Borchers, I. Schuberth, F. Alves Proof of Principle in the Selective Treatment of Cancer by Antibody Directed Enzyme Prodrug Therapy. The Development of a Highly Potent Prodrug. Angew. Chem. 2002, 114, 785-787; Angew. Chem., Int. Ed. 2002, 41, 759-761.
322 L.F. Tietze, W.-R. Krahnert Stereoselective Synthesis of Simplified Cephalostatin Analogues by Multifold Heck Reactions and their Biological Evaluation, Chem. Eur. J. 2002, 8, 2116-2125.
323 L.F. Tietze, T. Herzig, T. Feuerstein, I. Schuberth Synthesis and Biological Evaluation of Novel Analogs and Prodrugs of the Cytotoxic Antibiotic CC-1065 for a Selective Cancer Therapy. Eur. J. Org. Chem. 2002, 1634-1645.
324 F. Alves, U. Borchers, H. Keim, R. Fortte, J. Olschimke, W.F. Vogel, H. Halfter, L.F. Tietze Inhibition of EGF mediated receptor acitivity and cell proliferation by HK1-ceramide, a stable analogue of the ganglioside GM3-lactone. Glycobiology 2002, 12, 517-522.
325 L.F. Tietze, U. Griesbach, O. Elsner Efficient Synthesis of ortho -Carborane by Reaction of Propiolic acid tert-butyl ester with Decaborane(14). Synlett 2002, 1109-1110.
326 L.F. Tietze, H. Evers, E. Töpken A Novel Concept for Combinatorial Chemistry in Solution. Synthesis of Highly Substituted Pyrrolidines by Multicomponent Domino Reactions. Helvetica Chimica Acta 2002, 85, 4200-4205.
327 L.F. Tietze, J.K. Lohmann Synthesis of Novel Chiral Thiophene-, Benzothiophene- and Benzofuran-Oxazoline Ligands and their Use in the Enantioselective Pd-Catalyzed Allylation. Synlett 2002, 2083-2085.
328 L.F. Tietze, A. Cascaval Highly Functionalized Chroman-4-Ones via Four-Component Domino Reaction of Substituted 2-Bromoacetophenones. Analele Stiintifice Ale Universitatii "Al. I. Cuza" Iasi, Seria Chimie, tomul X, nr. 2, 2002.
329 L.F. Tietze, P. Steck High pressure in organic synthesis: Influence on selectivity in "High Pressure Chemistry" (Eds.: R. Eldik, F.-G. Klärner), Wiley-VCH, Weinheim, 2002, p. 239-283.


330 L.F. Tietze, F. Haunert, T. Feuerstein, T. Herzig A Concise and Efficient Synthesis of seco-Duocarmycin SA. Eur. J. Org. Chem. 2003, 562-566.
331 L.F. Tietze, T. Ramachandar, C. Vock Stereoselective Synthesis of New Enantiopure Building Blocks for the Preparation of Steroids. Synlett 2003, 118-120.
332 L.F. Tietze,U. Griesbach, I. Schuberth, U. Bothe, A. Marra, A. Dondoni Novel Carboranyl C-Glycosides for the Treatment of Cancer by Boron Neutron Capture Therapy. Chem. Eur. J. 2003, 9, 1296-1302.
333 L.F. Tietze, J. Looft, T. Feuerstein Synthesis of Ring Size seco-Analogs of the Antitumor Antibiotic CC-1065 by Two Consecutive Transition Metal-Initiated Transformations. Eur. J. Org. Chem. 2003, 2749-2755.
334 L.F. Tietze, K.M. Sommer,G. Schneider, P. Tapolcsanyi, J. Woelfling, P. Mueller,M. Noltemeyer, H. Terlau Novel medium ring sized estradiol derivatives by intramolecular Heck reactions. Synlett 2003, 1494-1496.
335 L.F. Tietze, T. Feuerstein Highly Selective Compounds for the Antibody-Directed Enzyme Prodrug Therapy of Cancer. Aust. J. Chem. 2003, 56, 841-854.
336 L.F. Tietze, S. Chandrasekhar, H. Bell Natural Product Hybrids as New Leads for Drug Discovery. Angew. Chem. 2003, 115, 4128-4160.; Angew. Chem. Int. Ed. Engl. 2003, 42, 3996-4028.
337 L.F. Tietze, N. Rackelmann, G. Sekar Catalyst-Controlled Stereoselective Combinatorial Synthesis. Angew. Chem. 2003, 115, 4386-4389.; Angew. Chem. Int. Ed. Engl. 2003, 42, 4254-4257.
338 K. Marten, T. Feuerstein, M. Funke, C. Engelke, L.F. Tietze, K. Nebendahl, L. Trümper, C. Jakob, E. Grabbe Multislice spiral computed tomography of an orthotopic severe combined immunodeficient mouse model for lung adenocarcinoma. J. Exp. Anim. Sci. 2003 42, 181-191.
339 J.J. Vanden Eynde, N. Labuche, Y. Van Haverbeke, L.F. Tietze Polymer-assisted synthesis of ethyl 2-amino-4,6-diarylpyrimidine-5-carboxylates. Arkivok 2003, 22-28.
340 L.F. Tietze, J.M. Wiegand, C. Vock Synthesis of enantiopure B-nor-steroids by multiple Pd-catalyzed transformations. J. Organomet. Chem. 2003, 687, 346-352.
341 L.F. Tietze, T. Feuerstein Enzyme and Proton-Activated Prodrugs for a Selective Cancer Therapy. Curr. Pharm. Des. 2003, 9, 2155-2175.


342 J. Wölfling, E. Frank, G. Schneider, L.F. Tietze Synthesis of Novel D-Secoestrone Isoquinuclidines by an Unpredicted Iminium Ion-Induced 1,5-Hydride Shift. Eur. J. Org. Chem. 2004, 90-100.
343 L.F. Tietze, N. Rackelmann Enantioselective Synthesis of Epi-Emetine Analogues: Control of the Facial Selectivity in a Three-Component Domino Knoevenagel-Hetero-Diels-Alder Reaction. Z. Naturforsch., B: Chem. Sci. 2004, 468-477.
344 L.F. Tietze J.K. Lohmann, C. Stadler Synthesis of Novel Highly Active Thiophene and Benzothiophene Containing Diphospine Ligands and their Use in the Asymetric Allylation of Catechol. Synlett 2004, 1113-1116.
345 L.F. Tietze, N. Rackelmann, L. Müller Enantioselective Total Syntheses of Ipecacuanha Alkaloid Emetine, the Alangium Alkaloid Tubulosine and a Novel Benzoquinolizidine Alkaloid by using a Domino Process. Chem. Eur. J. 2004, 10, 2722-2731.
346 L.F. Tietze, L.P. Lücke, F. Major, P. Müller Efficient Synthesis of an Enantiopure Thiasteroid by a Double Heck Reaction. Aust. J. Chem. 2004, 57, 635-640.
347 L.F. Tietze, S. Hölsken, J. Adrio, T. Kinzel, C. Wegner Facial-Selective Allylation of Methyl Ketones for the Asymmetric Synthesis of Tertiary Homoallylic Ethers. Synthesis 2004, 13, 2236-2239.
348 L.F. Tietze, I. Hiriyakkanavar, H.P. Bell Enantioselective Palladium-Catalyzed Transformations. Chem. Rev. 2004, 104, 3453-3516.
349 S.A.A. El Bialy, H. Braun, L.F. Tietze Synthesis of Azaspiro[4.4]nonanes as Key Structures of Several Bioactive Natural Products. Synthesis 2004, 14, 2249-2262.
350 S.A.A. El Bialy, H. Braun, L.F. Tietze A Highly Efficient Synthesis of the Erythrina and B-Homoerythrina Skeleton by an AlMe3-Mediated Domino Reaction. Angew. Chem. 2004, 116, 5505-5507; Angew. Chem., Int. Ed. 2004, 43, 5391-5393.
351 L.F. Tietze, J.M. Wiegand, C.A. Vock Synthesis of a Novel Enantiopure Spiro-b-norestradiol Analogue by Multiple Pd-Catalyzed Transformations. Eur. J. Org. Chem. 2004, 4107-4112.
352 L.F. Tietze, S.G. Stewart, M.E. Polomska, A. Modi, A. Zeeck Towards a Total Synthesis of the New Anticancer Agent Mensacarcin: Synthesis of the Carbocyclic Core. Chem. Eur. J. 2004, 10, 5233-5242.
353 L.F. Tietze, N.Rackelmann Domino reactions in the synthesis of heterocyclic natural products and analogs. Pure Appl. Chem. 2004, 76, 1967-1983.


354 L.F. Tietze, K.M. Sommer, J. Zinngrebe, F. Stecker Palladium-Catalyzed Enantioselective Domino Reaction for the Efficient Synthesis of Vitamin E. Angew. Chem. 2005, 117, 262-264; Angew. Chem., Int. Ed. 2005, 44, 257-259.
355 L.F. Tietze, S.G. Stewart, M.E. Polomska Intramolecular Heck Reactions for the Synthesis of the Novel Antibiotic Mensacarcin: Investigation of Catalytic, Electronic and Conjugative Effects in the Preparation of the Hexahydroanthracene Core. Eur. J. Org. Chem. 2005, 17521759.
356 L.F. Tietze, C. Güntner, K.M. Gericke,I. Schuberth, G. Bunkoczi A Diels-Alder Reaction for the Total Synthesis of the Novel Antibiotic Antitumor Agent Mensacarcin. Eur. J. Org. Chem. 2005, 2459-2467.
357 L.F. Tietze, I. Elghamry Linearly-p-Extended Porphyrins: Synthesis of Novel Tetrabenzoylporphyrins. J. Heterocycl. Chem. 2005, 42, 503-508.
358 S.A.A. El Bialy, H. Braun, L.F. Tietze Enantioselective Synthesis of a-Alkylmalates as the Pharmacophoric Group of Several Natural Alkaloids and Glycosides. Eur. J. Org. Chem. 2005, 2965-2972.
359 S.-B. Yang, F. Major, L. F. Tietze, M. Rupnik Block of Delayed-Rectifier Potassium Channels by Reduced Haloperidol and Related Compounds in Mouse Cortical Neurons. J. Pharmacol. Exp.Ther. 2005, 315, 352-362.
360 L.F. Tietze, A. Cascaval Highly Functionalized Chroman-4-Ones by a Three-Component Domino Reaction of some Halogenated 2-Hydroxypropiophenones. Analele Stiintifice ale Universitatii "Al. I. Cuza" din Iasi, Chimie 2005 13, 45-50.
361 L.F. Tietze, M.L. Birsa, A. Cascaval New 3-Amino-Chroman-4-Ones by a Three-Component Domino Reaction (3CDR) of Halogenated 2-Bromo-2'-Hydroxy-Propiophenones. Analele Stiintifice ale Universitatii "Al. I. Cuza" din Iasi, Chimie 2005 13, 91-95.
362 L.F. Tietze, N. Rackelmann The Domino-Knoevenagel-hetero-Diels-Alder Reaction and Related Transformations in "Multicomponent Reactions" (Eds.: Zhu, Bienaymé) Wiley-VCH, Weinheim, 2005, p. 121-168.


Last Update 10. Januar 2017 . Please report any error to Martina Pretor