Publikationen 1998
Publikationen 1999
Publikationen 2000
Publikationen
2001 Publikationsliste
Publikationen 1998
Publikationen 1999
Publikationen 2000
Publikationen
2001
| 255 | L.F. Tietze, G. Kettschau, J. A. Gewert and A. Schuffenhauer | Hetero-Diels-Alder Reactions of 1-Oxa-1,3-butadienes. Current Organic Chemistry 1998, 2, 19-62. |
| 256 | L.F. Tietze and R. Ferraccioli | Efficient Synthesis of Aza-Heterocycles by a Domino Process using an Inter- and an Intra- molecular Heck Reaction. Synlett 1998, 145-146. |
| 257 | L.F. Tietze, C. Wulff, C. Wegner, A. Schuffenhauer and K. Schiemann | Mechanistic Investigations on the Highly Stereoselectiv Allylation of Aldehydes with a Norpseudoephedrine Derivative. J. Am. Chem. Soc. 1998, 120, 4276-4280. |
| 258 | L.F. Tietze, T. Hippe and A. Steinmetz | Palladium-Catalyzed Allylic Substitution on Solid Support. Chem. Commun. 1998, 793-794. |
| 259 | L.F. Tietze and J. Görlitzer | Preparation of Chiral Building Blocks for a Highly Convergent Vitamin E Synthesis. Systematic Investigations on the Enantioselectivity of the Sharpless Bishydroxilation. Synthesis 1998, 873-878. |
| 260 | L.F. Tietze and U. Bothe | Ortho-Carboranyl Glycosides of Glucose, Mannose, Maltose and Lactose for Cancer Treatment by Boron Neutron-Capture Therapy. Chem. Eur. J. 1998, 4, 1179-1183. |
| 261 | L.F. Tietze and M. Lieb | Domino Reactions for Library Synthesis of Small Molecules in Combinatorial Chemistry. Curr. Opin. Chem. Biol. 1998, 2, 363-371. |
| 262 | L.F. Tietze, C.O. Janssen and J. Gewert | Synthesis of Neolacto Gaglioside LM1. Eur. J. Org. Chem. 1998, 1887-1894. |
| 263 | L.F. Tietze and D. Gretzke | Synthesis of Specifically Labelled Ganglioside [1c-13C]-GM3. Eur. J. Org. Chem. 1998, 1895-1899. |
| 264 | L.F. Tietze, A. Schuffenhauer and P.R. Schreiner | The Conformations of Chiral alpha,beta-Unsaturated Sulfoxides and their Complexes with Lewis Acids. J. Am. Chem. Soc. 1998, 120, 7952-7958. |
| 265 | L.F. Tietze, C. Wegner and C. Wulff | Highly Selective Allylation of Alkyl Methyl Ketones in the Presence of Chiral 2-Amino Alcohole-Derivatives. Eur. J. Org. Chem. 1998, 1639-1644. |
| 266 | L.F. Tietze and A. Schuffenhauer | Synthesis of Tetrahydro- and Dihydropyridines by Hetero-Diels-Alder Reactions of Enantiopure alpha,beta-Unsaturated Sulfinimines. Eur. J. Org. Chem. 1998, 1629-1637. |
| 267 | L.F. Tietze, W. Buhr, J. Looft and T. Grote | Efficient Synthesis of the Pharmacophore of the Highly Potent Antitumor Antibiotic CC-1065. Chem. Eur. J. 1998, 4, 1554-1560. |
| 268 | L.F. Tietze, K. Schiemann, C. Wegner and C. Wulff | Synthesis of Enantiopure Homoallylic Alcohols by a Highly Selective Asymetric Allylation of Ketones. Chem. Eur. J. 1998, 4, 1862-1869. |
| 269 | L.F. Tietze, T. Pfeiffer and A. Schuffenhauer | Stereoselective Intramolecular Hetero-Diels-Alder Reactions of Cyclic Benzylidenesulfoxides and DFT Calculations on the Transition Structure. Eur. J. Org. Chem. 1998, 2733-2741. |
| 270 | L.F. Tietze, T. Nöbel and M. Spescha | Synthesis of Enantiopure Estron via a Double Heck-Reaction. J. Am. Chem. Soc. 1998, 120, 8971-8977. |
| 271 | J. Wölfling, E. Frank, Gy. Schneider, Maria Teresa Bes and L.F. Tietze | Synthesis of Azasteroids and D-Homosteroids by Intramolecular Cyclization Reactions of Steriod Arylimines. Synlett 1998, 1205-1206. |
| 272 | L.F. Tietze, Gy. Schneider, J. Wölfling, T. Nöbel, C. Wulff, I. Schuberth and A. Rübeling | Efficient Synthesis of a Novel Estrone-Talaromycin Hybrid Natural Product. Angew. Chem. 1998, 110, 2644-2646.; Angew. Chem., Int. Ed. 1998, 37, 2469-2470. |
| 273 | L. F. Tietze and C. Schünke | Synthesis of Enantiomerically pure trans-1,2-disubstituted Cyclopentanes and Cyclohexanes by Intramolecular Allylsilane Addition to Chiral Alkylidene 1,3-dicarbonyl Compounds. Eur. J. Org. Chem. 1998, 2089-2099. |
| 274 | J. Wölfling, E. Frank, Gy. Schneider, M. T. Bes and L.F. Tietze | A Hexacyclic Estrone Derivative. Acta Cryst. 1998, C54, 1341-1343. |
| 275 | L. F. Tietze and K. Böge | Synthesis of Alkyl Polyclycosides. Effect of Catalyst-type on Reaction Rate and Product Composition. Fett/Lipid. 1998, 100, 36-41. |
| 276 | L.F. Tietze, M. Henrich, A. Niklaus and M. Buback | Effect of High Pressure on the Diastereoselectivity of Intermolecular Diels-Alder-Reactions. Chem. Eur. J. 1999, 5, 297-304. |
| 277 | J. Wölfling, E. Frank, Gy. Schneider and L.F. Tietze | Synthesis of Unusual Bridged Steroid Alkaloids by an Iminium Ion Induced 1,5-Shift of a Benzylic Hydride. Angew. Chem. 1999, 111, 151-152.; Angew. Chem., Int. Ed. 1999, 38, 200-201. |
| 278 | Lutz F. Tietze, J. Görlitzer, A. Schuffenhauer and M. Hübner |
Enantioselective Synthesis of the Chromane Moiety of Vitamin E, Eur. J. Org. Chem. 1999, 1075-1084. |
| 279 | L.F. Tietze and Y. Zhou | Highly Efficient, Enantioselective Total Synthesis of the Active Anti-Influenza A Virus Indole Alkaloid Hirsutine and Related Compounds by Domino Reactions. Angew. Chem. 1999, 111, 2076-2078.; Angew. Chem., Int. Ed. 1999, 38, 2045-2047. |
| 280 | L.F. Tietze, C. Wegener and C. Wulff | First Total Synthesis and Determination of the Absolute Configuration of the Stress Factor (+)-Hydroxymyoporone. Chem. Eur. J. 1999, 111, 2076-2078. |
| 281 | L.F. Tietze, K. Thede and F. Sannicolo | Regio- and enantioselective Heck reactions of aryl and alkenyl triflates with the new chiral ligand (R)-BITIANP. Chem. Comm. 1999, 1811-1812. | 282 | J. Wölfling, E. Frank, Gy. Schneider and L.F. Tietze | Synthesis of Novel Steroid Alkaloids by Cyclization of Arylimines from Estrone. Eur. J. Org. Chem. 1999, 3013-3020. |
| 283 | L.F. Tietze and H. Schirok | Enantioselective Highly Efficient Synthesis of (-)-Cephalotaxine Using Two Palladium-Catalyzed Transformations. J. Am. Chem. Soc. 1999, 121, 10264-10269. |
| 284 | O.A. Attanasi, P. Filippone, B. Guido, T. Hippe, F. Mantellini and L. F. Tietze | First Preparation and Reaction of Polymer-Bound 1,2-diaza-1,3-butadienes. A Convenient Entry to 4-Triphenylphosphoranyliden-4,5-dihydropyrazol-5-ones. Tetrahedron Letters 1999, 40, 9277-9280. |
| 285 | L.F. Tietze, B. Weigand and C. Wulff | A Mild and Efficient Method for the Preparation of 1,3-Dithianes from Aldehydes and Ketones. Synthesis, 2000, 69-71. |
| 286 | L.F. Tietze, U. Bothe and I. Schuberth | Preparation of a New Carboranyl Lactoside for the Treatment of Cancer by Boron Neutron Capture Therapy: Synthesis and Toxicity of Fluoro Carboranyl Glycosides for in vivo 19F NMR Spectroscopy. Chem. Eur. J. 2000, 6, 836-842. |
| 287 | L.F. Tietze, H. Schirok and M. Wöhrmann | Palladium Catalyzed Synthesis of Cephalotaxine Analogues. Chem. Eur. J. 2000, 6, 510-518. |
| 288 | L.F. Tietze, K. Thede, R. Schimpf and F. Sannicolo | Enantioselective Synthesis of Tetrahydroisoquinolines and Benzazepines by Silane Terminated Heck Reactions with the New Chiral Ligands (+)-TMBTP and (R)-BITIANP. Chem. Comm. 2000, 583-584. |
| 289 | L.F. Tietze and S. Petersen | Stereoselective Total Synthesis of a Novel D-Homosteroid by a Two-Fold Heck Reaction. Eur. J. Org. Chem.. 2000, 1827-1830. |
| 290 | L.F. Tietze and A. Modi | Regioselective Silane-Terminated Intramolecular Heck Reaction with Alkenyl Triflates and Alkenyl Iodides. Eur. J. Org. Chem. 2000, 1959-1964. |
| 291 | L.F. Tietze, H. Keim, C.O. Janßen, C. Tappertzhofen and J. Olschimke | Synthesis of a Novel Ether-Bridged GM3-Lactone Analogue as a Target for an Antibody-Based Cancer Therapy. Chem. Eur. J. 2000, 6, 2801-2808. |
| 292 | L.F. Tietze, Y. Zhou and E. Töpken | Synthesis of Simple Enantiopure Tetrahydro-b-carbolines and Tetrahydroisoquinolines. Eur. J. Org. Chem. 2000, 2247-2252. |
| 293 | L.F. Tietze, H. Schirok, M. Wöhrmann and K. Schrader | Efficient Synthesis of Six-Membered Ring D Analogues of the Pentacyclic Cephalotaxine by Two Palladium-Catalyzed Reactions. Eur. J. Org. Chem. 2000, 2433-2444. |
| 294 | L.F. Tietze and A. Modi | Multi-component Domino Reactions for the Synthesis of Biological Active Natural Products and Drugs. Medicinal Research Reviews 2000, 20, 304-322. |
| 295 | L.F. Tietze, G. Schneider, J. Wölfling, A. Fecher, T. Nöbel, S. Petersen, I. Schuberth and C. Wulff | A Novel Approach in Combinatorial Chemistry. Synthesis of Estrone-Talaromycin Natural Product Hybrids. Chem. Eur. J. 2000, 6, 3755-3760. |
| 296 | L.F. Tietze and K. Thede | Highly Regio- and Enantioselective Heck Reactions of N-Substituted 2-Pyrroline with the Novel Chiral Ligand BITIANP. Synlett, 2000, 10, 1470-1472. |
| 297 | L.F. Tietze and F. Haunert | Domino Reactions in Organic Synthesis. An Approach to Efficiency, Elegance, Ecological Benefit, Economic Advantage and Preservation of our Resources in Chemical Transformations in "Stimulating Concepts in Chemistry" (Eds.: M. Shibasaki, J.F.Stoddart and F. Vögtle). Wiley-VCH, Weinheim, 2000, p. 39-64. |
| 298 | A. Kirschning, Guang-wu Chen, G. Dräger, I. Schuberth and L.F. Tietze | Syntheses and Biological Evaluation of New Glyco-modified Angucyclin-antibiotics. Bioorg. Med. Chem. 2000, 8, 2347-2354. |
| 299 | F. Alves, U. Borchers, B. Padge, H. Augustin, K. Nebendahl, G. Klöppel and L.F. Tietze | Inhibitory Effect of a Matrix Metalloproteinase Inhibitor on Growth and Spread of Human Pancreatic Ductal Adenocarcinoma Evaluated in an Orthotopic SCID-Mouse Model. Cancer Lett. 2001, 165, 161-170. |
| 300 | L.F. Tietze, B. Weigand, L. Völkel, C. Wulff and C. Bittner | Synthesis of Enantiopure Homoallylic Ethers by Reagent Controlled Facial Selective Allylation of Chiral Ketones. Chem. Eur. J. 2001, 7, 161-168. | 301 | L.F. Tietze, G. Kettschau, U. Heuschert and G. Nordmann | Highly Efficient Synthesis of Linear Pyrrol Oligomers by Two-Fold Heck Reactions. Chem. Eur. J. 2001, 7, 368-373. |
| 302 | L.F. Tietze, U. Bothe, U. Griesbach, M. Nakaichi, T. Hasegawa, H. Nakamura, Y. Yamamoto | Carboranyl Bisglycosides for the Treatment of Cancer by Boron Neutron Capture Therapy. ChemBioChem. 2001, 2, 326-334. |
| 303 | L.F. Tietze and L. Völkel | Total Synthesis of the Macrolide Antibiotic 5,6-Dihydrocineromycin B. Angew. Chem. 2001, 113, 925-927.; Angew. Chemie Int. Ed. Engl. 2001, 40, 901-902. |
| 304 | L.F. Tietze and S. Petersen | Stereoselective Synthesis of Novel 19-Nor-Steroids by a Double Heck Reaction. Eur. J. Org. Chem. 2001, 1619-1624. |
| 305 | L.F. Tietze, H. Evers and E. Töpken | Novel Concept in Combinatorial Chemistry in Solution with the Advantages of Solid-Phase Synthesis: Formation of N-Betaines by Multicomponent Domino Reactions. Angew. Chem. 2001, 113, 927-929; Angew. Chem. Int. Ed. Engl. 2001, 40, 903-905. |
| 306 | L.F. Tietze, L. Völkel, C. Wulff, B. Weigand, C. Bittner, P. McGrath, K. Johnson and M. Schäfer | Facial Selective Allylation of Methyl Ketones for the Asymmetric Synthesis of a-Substituted Tertiary Homoallylic Ethers. Chem. Eur. J. 2001, 7, 1304-1308. |
| 307 | L.F. Tietze and G. Nordmann | Synthesis of a Linear Oligomeric Styrylpyrrole Using Multiple Heck and Wittig Reactions. Synlett 2001, 337-340. |
| 308 | L.F. Tietze, C. Ott, H. Geißler and F. Haunert | Regioselective Reduction and Ring Cleavage of Polycyclic Barbituric Acid Analogues Derived from Intramolecular Hetero-Diels-Alder Reactions. Eur. J. Org. Chem. 2001, 1625-1630. |
| 309 | L.F. Tietze, H. Evers, T. Hippe A. Steinmetz and E. Töpken | Solid Phase Synthesis of Substituted Pyrazolones from Polymer bound b-keto Esters. Eur. J. Org. Chem. 2001, 1631-1634. |
| 310 | L.F. Tietze and W.R. Krahnert | Stereoselective Synthesis of Structurally Simplified Cephalostatin Analogues by Morefold Heck Reactions. Synlett 2001, 560-562. |
| 311 | L.F. Tietze, U. Bothe, U. Griesbach, M. Nakaichi, T. Hasegawa, H. Nakamura and Y. Yamamoto | Ortho-Carboranyl Glycosides for the Treatment of Cancer by Boron Neutron Capture Therapy, Bioorg. Med. Chem. 2001, 9, 1747-1752. |
| 312 | L.F. Tietze, M. Lieb, T. Herzig, F. Haunert and I. Schuberth | A Strategy for Tumor-Selective Chemotherapy by Enzymatic Liberation of seco-Duocarmycin SA-Derivatives from Non-toxic Prodrugs. Bioorg. Med. Chem 2001, 9, 1929-1939. |
| 313 | O.A. Attanasi, L. De Crescentini, P. Filippone, F. Mantellini and L.F. Tietze | Solid-phase synthesis of 4-triphenylphosphoranylidene-4,5-dihydropyrazol-5-ones, 4-aminocarbonyl-pyrroles, 4-methoxy-1H-pyrazol-5(2H)-ones and 2-thiazolin-4-ones from polymer-bound 1,2-diaza-1,3-butadienes. Tetrahedron 2001, 5855-5863. |
| 314 | L.F. Tietze and G. Nordmann | A Novel Palladium-Catalyzed Domino-Tsuji-Trost-Process for the Synthesis of Tetrahydroanthracenes. Eur. J. Org. Chem. 2001, 3247-3253. |
| 315 | L.F. Tietze, T. Herzig, A. Fecher, F. Haunert and I. Schuberth | Highly Selective Glycosylated Prodrugs of Cytostatic CC-1065 Analogs for Antibody Directed Enzyme Tumor therapy. ChemBioChem 2001, 758-765. |
| 316 | L.F. Tietze and P.L. Steck | A domino spirocyclization to form lactams. Eur. J. Org. Chem. 2001, 4353-4356. |
| 317 | L.F. Tietze, C. Ott and F. Haunert | Efficient and regioselective synthesis of bridged ring systems by domino Knoevenagel hetero-Diels-Alder reaction Can. J. Chem. 2001, 79, 1511-1514. |
| 318 | P.L. Steck, M. Wöhrmann, L.F. Tietze | Synthesis of oxo-cephalotaxine analogs applying two palladium-catalyzed transformations. Abstracts of Papers, 221st ACS National Meeting, San Diego, CA, United States, April 1-5 2001, 79, ORGN-380. |
Last Update 29. Jan 2003. Please report any error to Martina Pretor