| 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, 1752–1759. |
| 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. |
Publikationen 2002 