| 363 |
L.F. Tietze, F. Major |
Synthesis of New Water-Soluble DNA-Binding Subunits for Analogues of the
Cytotoxic Antibiotic CC-1065 and Their Prodrugs.
Eur. J. Org. Chem. 2006, 2314-2321.
Online |
| 364 |
L.F. Tietze, G. Brasche, C. Stadler, A. Grube, N. Böhnke |
Multiple Palladium-Catalyzed Reactions for the Synthesis of Analogues of the Highly Potent
Insecticide Spinosyn A. Angew. Chem. 2006, 118, 5137-5140;
Angew. Chem., Int. Ed. 2006, 45, 5015-5018.
Online |
| 365 |
L.F. Tietze, T. Kinzel, S. Schmatz |
Origin of Syn/Anti Diastereoselectivity in Aldehyde and
Ketone Crotylation Reactions: A Combined Theoretical and Experimental Study.
J. Am. Chem. Soc. 2006, 128, 11483-11495.
Online |
| 366 |
L.F. Tietze, B. Krewer, H. Frauendorf, F. Major, I. Schuberth |
Investigation of Reactivity and Selectivity of DNA-Alkylating Duocarmycin Analogues by
High-Resolution Mass Spectrometry.
Angew. Chem. 2006, 118, 6720-6724;
Angew. Chem., Int. Ed. 2006, 45, 6570-6574.
Online |
| 367 |
L.F. Tietze, F. Major, I. Schuberth |
Antitumor Agents: Development of Highly Potent Glycosidic Duocarmycin Analogues for Selective Cancer Therapy.
Angew. Chem. 2006, 118, 6724-6727;
Angew. Chem., Int. Ed. 2006, 45, 6574-6577.
Online |
| 368 |
L.F. Tietze, F. Lotz |
Pd-Catalysed Domino Arylation/CH Activation for the Synthesis of Acenaphthylenes.
Eur. J. Org. Chem. 2006, 4676-4684.
Online |
| 369 |
L.F. Tietze F. Stecker, J. Zinngrebe, K. M. Sommer |
Enantioselective Palladium-Catalyzed Total Synthesis of Vitamin E by
Employing a Domino Wacker-Heck Reaction.
Chem. Eur. J. 2006, 12, 8770-8776.
Online |
| 370 |
L.F. Tietze K. M. Gericke, R. R. Singidi |
Enantioselective Total Synthesis and Structure
Determination of the Antiherpetic Anthrapyran Antibiotic AH-1763 IIa.
Angew. Chem. 2006, 118, 7146-7150;
Angew. Chem., Int. Ed. 2006, 45, 6990-6993.
Online |
| 371 |
L.F. Tietze, K. M. Gericke, C. Güntner |
First Total Synthesis of the Bioactive Anthraquinone Kwanzoquinone C and
Related Natural Products by a Diels-Alder Approach.
Eur. J. Org. Chem. 2006, 4910-4915.
Online |
| 372 |
L.F. Tietze, R.R. Singidi, K.M. Gericke |
First Enantioselective Total Synthesis and Structure Determination of the
Anthrapyran Metabolite g-Indomycinone.
Org. Lett. 2006, 8, 5873-5876.
Online |
| 373 |
L.F. Tietze, K.F. Wilckens, S. Yilmaz, F. Stecker, J. Zinngrebe |
Synthesis of 2,3-Dihydrobenzo[1,4]dioxins and -oxazins via a Domino Wacker-Heck Reaction.
Heterocycles 2006, 70, 309-319.
Online |
| 374 |
L.F. Tietze, F. Lotz |
Asymmetric Heck and other Palladium Catalysed Reactions in "Asymmetric Synthesis -
The Essentials"(Eds.: Christmann, Bräse)
Wiley-VCH, Weinheim, 2006, p. 147-152. |
| 375 |
L.F. Tietze, N. Böhnke, G. Brasche |
Preparation of (2R)-2-acetoxy-D-forosamine for the total synthesis of spinosyns.
Arkivoc 2007, 12-21. Online |
| 376 |
L.F. Tietze, C. Stadler, N. Böhnke, G. Brasche, A. Grube |
Synthesis of Enantiomerically Pure Cyclopentene Building Blocks.
Synlett 2007, 485-487. Online |
| 377 |
L.F. Tietze, K.M. Gericke, R.R. Singidi, I. Schuberth |
Novel strategies for the synthesis of anthrapyran antibiotics: discovery of a
new antitumor agent and total synthesis of (S)-espicufolin.
Org. Biomol. Chem. 2007, 5, 1191-1200.
Online |
| 378 |
L.F. Tietze, T. Kinzel |
Synthesis of natural products and analogs using multiple
Pd-catalyzed transformations.
Pure Appl. Chem. 2007, 79, 629-650.
Online |
| 379 |
L.F. Tietze, F. Major, I. Schuberth, D.A. Spiegl, B. Krewer,
K. Maksimenka, G. Bringmann, J. Magull |
Selective Treatment of Cancer: Synthesis, Biological Evaluation and
Structural Elucidation of Novel Analogues of the Antibiotic CC-1065 and the
Duocarmycins.
Chem. Eur. J. 2007, 13, 4396-4409.
Online |
| 380 |
L.F. Tietze, H. Braun, P.L. Steck, S.A.A. El Bialy,
N. Tölle, A. Düfert |
Efficient synthesis of cephalotaxine- and deoxyharringtonine
analogues by a trimethylaluminium-mediated domino reaction.
Tetrahedron 2007, 6437-6445.
Online |
| 381 |
L.F. Tietze, G. Brasche, A. Grube, N. Böhnke, C. Stadler |
Synthesis of Novel Spinosyn A Analogues by Pd-Mediated Transformations.
Chem. Eur. J. 2007, 13, 8543-8563.
Online |
| 382 |
L.F. Tietze, K. M. Gericke, I. Schuberth |
Synthesis of Highly Functionalized Anthraquinones and Evaluation of Their Antitumor Activity.
Eur. J. Org. Chem. 2007, 4563-4577.
Online |
| 383 |
L.F. Tietze, R.R. Singidi, K.M. Gericke |
Total Synthesis of the Proposed Structure of the Anthrapyran Metabolite
δ-Indomycinone.
Chem. Eur. J. 2007, 13, 9939-9947.
Online |
| 384 |
L.F. Tietze, R.R. Singidi, K.M. Gericke, H. Böckemeier, H. Laatsch |
Isolation, Enantioselective Total Synthesis and Structure Determination of the Anthrapyran Metabolite.
Eur. J. Org. Chem. 2007, 5875-5878.
Online |
| 385 |
L.F. Tietze, J. Zinngrebe, D.A. Spiegl, F. Stecker |
Palladium-catalyzed Domino-Wacker-Carbonylation Reaction for the Enantioselective Synthesis of Chromans and Benzodioxins.
Heterocycles 2007, 74, 473-489.
Online |
| 386 |
L.F. Tietze, C. Raith, C.C. Brazel, S. Hölsken, J. Magull |
Enantioselective Synthesis of 2-Substituted Alcohols Using
(+)-(1S,2S)-Pseudoephedrine as Chiral Auxiliary.
Synthesis 2008, 229-236.
Online |
| 387 |
L.F. Tietze, H.J. Schuster, S.M. Hampel, S. Rühl, R. Pfoh |
Enantio- and Diastereoselective Synthesis of Duocarmycine-Based Prodrugs for a Selective Treatment of Cancer by Epoxide Opening
Chem. Eur. J. 2008, 14, 895-901.
Online |
| 388 |
L.F. Tietze, I. Krimmelbein |
Enantioselective Total Synthesis of the Oral Contraceptive Desogestrel via a Double Heck Reaction.
Chem. Eur. J. 2008, 14, 1541-1551.
Online |
| 389 |
L.F. Tietze, N. Tölle, C. Noll |
Highly Efficient Domino Reaction for the Synthesis of the Erythrina and B-Homoerythrina Alkaloid Skeleton.
Synlett 2008, 525-528.
Online |
| 390 |
L.F. Tietze, T. Redert, H.P. Bell, S. Hellkamp, L.M. Levy |
Efficient Synthesis of the Structural Core of Tetracyclines by a Palladium-Catalyzed Domino Tsuji-Trost-Heck-Mizoroki Reaction.
Chem. Eur. J. 2008, 14, 2527-2535.
Online |
| 391 |
L.F. Tietze, O. Panknin, F. Major, B. Krewer |
Synthesis of a Novel Pentagastrin-Drug Conjugate for a Targeted Tumor Therapy.
Chem. Eur. J. 2008, 14, 2811-2818.
Online |
| 392 |
L.F. Tietze, T. Kinzel, S. Schmatz |
Determination of the Origin of Stereoselectivity in Multiple-Transition-State Reactions Using DFT Calculations:
Enantioselective Synthesis of Homoallylic Alcohols from Aliphatic Methyl Ketones via an Auxiliary-Mediated Allylation.
J. Am. Chem. Soc. 2008, 130, 4386-4395.
Online |
| 393 |
L.F. Tietze, C.A. Vock, I.K. Krimmelbein, J.M. Wiegand, L. Nacke, T. Ramachandar, K.M.D. Islam, C. Gatz |
Synthesis of Novel Structurally Simplified Estrogen Analogues.
Chem. Eur. J. 2008, 14, 3670-3679.
Online |
| 394 |
L.F. Tietze, D. Liu |
Continuous-flow microreactor multi-step synthesis of an aminonaphthalene derivative as starting material for the preparation of novel anticancer agents.
Arkivoc 2008, 193-210.
Online |
| 395 |
I. Elghamry, L.F. Tietze |
Microwave assisted synthesis of novel annealed porphyrins.
Tetrahedron Lett. 2008, 49, 3972-3975.
Online |
| 396 |
L.F. Tietze, O. Panknin, B. Krewer, F. Major, I. Schuberth |
Synthesis and Biological Evaluation of a Novel Pentagastrin-Toxin Conjugate Designed for a Targeted Prodrug Monotherapy of Cancer.
Int. J. Mol. Sci. 2008, 9, 821-837.
Online |
| 397 |
L.F. Tietze, C.C. Brazel, S. Hölsken, J. Magull, A. Ringe |
Total Synthesis of Polyoxygenated Cembrenes.
Angew. Chem. 2008, 120, 5324-5327;
Angew. Chem., Int. Ed. 2008, 47, 5246-5249.
Online |
| 398 |
L.F. Tietze, H.J. Schuster, K. Schmuck, I. Schuberth, F. Alves |
Duocarmycin based Prodrugs for Cancer Prodrug-Monotherapy.
Bioorg. Med. Chem. 2008, 16, 6312-6318.
Online |
| 399 |
D.B. Werz, H. Schuster, L.F. Tietze |
Fast and Efficient Preparation of an α-Fucosyl Building Block by Reductive
1,2-Benzylidene Ring Opening Reaction.
Synlett 2008, 1969-1972.
Online |
| 400 |
L.F. Tietze, D.A. Spiegl, F. Stecker, J. Major, C. Raith, C. Grosse |
Stereoselective Synthesis of 4-Dehydroxydiversonol Employing Enantioselective Palladium-Catalysed Domino Reactions.
Chem. Eur. J. 2008, 14, 8956-8963.
Online |
| 401 |
L.F. Tietze, J.M. von Hof, B. Krewer, M. Müller, F. Major, H.J. Schuster, I. Schuberth |
Asymmetric Synthesis and Biological Evaluation of New Glycosidic Prodrugs for a Selective Cancer Therapy.
ChemMedChem 2008, 3, 1946-1955.
Online |
| 402 |
L.F. Tietze, T. Kinzel, S. Schmatz |
Stereoselective Allylation of Ketones: Explanation for the Unusual Inversion of the Induced Stereochemistry in the
Auxiliary-Mediated Crotylation and Pentylation of Butanone by DFT Calculations.
Chem. Eur. J. 2009, 15, 1706-1712.
Online |
| 403 |
K.M.D. Islam, M. Dilcher, C. Thurow, C. Vock, I.K. Krimmelbein, L.F. Tietze, V. Gonzalez, H. Zhao, C. Gatz |
Directed evolution of estrogen receptor proteins with altered ligand-binding specificities.
PEDS 2009, 22, 45-52.
Online |
| 404 |
L.F. Tietze, H.J. Schuster, B. Krewer, I. Schuberth |
Synthesis and Biological Studies of Different Duocarmycin based Glycosidic Prodrugs for their use in
Antibody-Directed Enzyme Prodrug Therapy. J. Med. Chem. 2009, 52, 537-543.
Online |
| 405 |
L.F. Tietze, L. Levy |
The Mizoroki-Heck Reaction in Domino Processes in "The Mizoroki-Heck Reaction" (Ed.: M. Oestreich)
Wiley-VCH, Chichester, 2009, p. 281-344. |
| 406 |
L.F. Tietze, T. Kinzel, C. Brazel |
The Domino Multicomponent Allylation Reaction for the Stereoselective Synthesis of Homoallylic Alcohols.
Acc. Chem. Res. 2009, 42, 367-378.
Online |
| 407 |
L.F. Tietze, B. Krewer |
Novel Analogues of CC-1065 and the Duocarmycins for the Use in Targeted Tumour Therapies.
Anti-Cancer Agents Med. Chem. 2009, 9, 304-325.
Online |
| 408 |
L.F. Tietze, A. Heins, M. Soleiman-Beigi, C. Raith |
Synthesis of Annulated 1,4-Dioxanes and Perhydro-1,4-oxazines by Domino-Wacker-Carbonylation and
Domino-Wacker-Mizoroki-Heck Reactions.
Heterocycles 2009, 77, 1123-1146.
Online |
| 409 |
C. Dullin, M. Zientkowska, J. Napp, J. Missbach-Guentner, H.-W. Krell, F. Müller, E. Grabbe, L.F. Tietze, F. Alves |
Semi-automatic landmark-based 2D-3D image fusion in living mice:
Correlation of near-infrared fluorescence imaging of Cy5.5 labeled antibodies with flat-panel volume computed tomography.
Molecular Imaging 2009, 8, 1-14.
Online |
| 410 |
L.F. Tietze, D.A. Spiegl, C.C. Brazel |
Domino Reactions for the Efficient Synthesis of Natural Products in
"Experiments in Green and Sustainable Chemistry" (Ed.: H.W. Roesky, D.K. Kennepohl)
Wiley-VCH, Weinheim, 2009, p. 158-167. |
| 411 |
F. Alves, C. Dullin, J. Napp, J. Missbach-Guentner, K. Jannasch, J. Mathejczyk, L.A. Pardo, W. Stühmer, L.F. Tietze |
Concept of a selective tumour therapy and its evaluation by near-infrared fluorescence
imaging and flat-panel volume computed tomography in mice.
Eur. J. Radiol. 2009, 70, 286-293.
Online |
| 412 |
L.F. Tietze, T. Kinzel, T. Wolfram |
Asymmetric Allylation of Methyl Ketones Using Chiral Phenyl Carbinols.
Chem. Eur. J. 2009, 15, 6199-6210.
Online |
| 413 |
L.F. Tietze, C.A. Vock, I.K. Krimmelbein, L. Nacke |
Synthesis of Novel Structurally Simplified Estrogen Analogues with Electron-Donating Groups in Ring A.
Synthesis 2009, 2040-2060.
Online |
| 414 |
L.F. Tietze, N. Böhnke, S. Dietz |
Synthesis of the Deoxyaminosugar(+)-D-Forosamine via a Novel
Domino-Knoevenagel-Hetero-Diels-Alder Reaction.
Org. Lett. 2009, 11, 2948-2950.
Online |
| 415 |
L.F. Tietze, B. Krewer, H. Frauendorf |
Investigation of the transformations of a novel anti-cancer agent
combining HPLC, HPLC-MS and direct ESI-HRMS analyses.
Anal. Bioanal. Chem. 2009, 437-448.
Online |
| 416 |
L.F. Tietze, B. Krewer |
Antibody-Directed Enzyme Prodrug Therapy: A Promising Approach for a
Selective Treatment of Cancer Based on Prodrugs and Monoclonal Antibodies.
Chem. Biol. Drug Des. 2009, 74, 205-211.
Online |
| 417 |
L.F. Tietze, B. Krewer, F. Major, I. Schuberth |
CD-spectroscopy as a powerful tool for investigating the mode of action of unmodified drugs in live cells.
J. Am. Chem. Soc. 2009, 131, 13031-13036.
Online |
| 418 |
L.F. Tietze, B. Krewer, H. Frauendorf |
Probing the mechanism of action of potential anticancer agents at a molecular
level using electrospray ionisation Fourier transform ion cyclotron resonance mass spectrometry.
Eur. J. Mass Spectrom. 2009, 15, 661-672.
Online |
| 419 |
L.F. Tietze, B. Krewer, J.M. von Hof, H. Frauendorf, I. Schuberth |
Determination of the Biological Activity and Structure Activity Relationships of Drugs Based on
the Highly Cytotoxic Duocarmycins and CC-1065.
Toxins 2009, 1, 134-150.
Online |
| 420 |
L.F. Tietze, N. Tölle, D. Kratzert, D. Stalke |
Efficient Formal Total Synthesis of the Erythrina Alkaloid (+)-Erysotramidine Using a Domino Process.
Org. Lett. 2009, 11, 5230-5233.
Online |
| 421 |
L.F. Tietze, A. Düfert, F. Lotz, L. Sölter, K. Oum, T. Lenzer, T. Beck, R. Herbst-Irmer |
Synthesis of Chiroptical Molecular Switches by Pd-Catalyzed Domino Reactions.
J. Am. Chem. Soc. 2009, 131, 17879-17884.
Online |
| 422 |
S.A. Opiyo, J.A. Ogur, L.O.A. Manguro, L.F. Tietze, H. Schuster |
A new sterol diglycoside from Conyza floribunda.
S. Afr. J. Chem. 2009, 62, 163-167.
Online |
| 423 |
L.L. Bajohr, L. Ma, C. Platte, O. Liesenfeld, L.F. Tietze, U. Groß, W. Bohne |
In-vitro and in-vivo activity of 1-hydroxy-2-alkyl-4(1H)quinolone derivatives against Toxoplasma gondii.
Antimicrob. Agents Chemother. 2010, 54, 517-521.
Online |
| 424 |
M. Schubert, A.N. Melnikova, N. Mesecke, E.K. Zubkova, F. Fortte, D.R. Batashev, I. Barth, N. Sauer, Y.V. Gamalei, N.S. Mamushina, L.F. Tietze, O.V. Voitsekhovskaja, K. Pawlowski |
Two novel disaccharides, rutinose and methylrutinose, are involved in carbon metabolism in Datisca glomerata.
Planta 2010, 231, 507-521.
Online |
| 425 |
H.J. Schuster, B. Krewer, J.M. von Hof, K. Schmuck, I. Schuberth, F. Alves, L.F. Tietze |
Synthesis of the first spacer containing prodrug of a duocarmycin analogue and determination of its biological activity.
Org. Biomol. Chem. 2010, 8, 1833-1842.
Online |
| 426 |
L.F. Tietze, A. Düfert |
Multiple Pd-catalyzed reactions in the synthesis of natural products, drugs, and materials.
Pure Appl. Chem. 2010, 82, 1375-1392.
Online |
| 427 |
L.F. Tietze, A. Düfert |
Domino Reactions Involving Catalytic Enantioselective Conjugate Additions in
"Catalytic Asymmetric Conjugate Reactions" (Ed.: A. Cordova)
Wiley-VCH, Weinheim, 2010, p. 321-350. |
| 428 |
L.F. Tietze, S. Biller, T. Wolfram |
First Enantioselective Total Synthesis of the Reported Structure of (R)-(+)-Orizaterpenyl Benzoate
Using an Asymmetric Allylation of a Prochiral Ketone in a Domino Process.
Synlett 2010, 2130-2132.
Online |
| 429 |
L.F. Tietze, J.M. von Hof, M. Müller, B. Krewer, I. Schuberth |
Glycosidic Prodrugs of Highly Potent Bifunctional Duocarmycin Derivatives for Selective Treatment of Cancer.
Angew. Chem. 2010, 122, 7494-7497.
Angew. Chem., Int. Ed. 2010, 49, 7336-7339.
Online |
| 430 |
L.F. Tietze, H.J. Schuster, J.M. von Hof, S.M. Hampel, J.F. Colunga, M. John |
Atropisomerism of Aromatic Carbamates.
Chem. Eur. J. 2010, 16, 12678-12682.
Online |
| 431 |
L.F. Tietze, F. Behrendt, F. Major, B. Krewer, J.M. von Hof |
Synthesis of Fluorescence Labeled Glycosidic Prodrugs Based on the Cytotoxic Antibiotic Duocarmycin.
Eur. J. Org. Chem. 2010, 6909-6921.
Online |
| 432 |
L.F. Tietze, L. Ma |
Synthesis of Novel 1-Hydroxyquinolones with High Anti-Toxoplasma Activity.
Heterocycles 2010, 82, 377-396.
Online |
| 433 |
L.F. Tietze, K. Schmuck, H.J. Schuster, M. Müller, I. Schuberth |
Synthesis and Biological Evaluation of Prodrugs Based on the Natural Antibiotic Duocarmycin for Use in ADEPT and PMT.
Chem. Eur. J. 2011, 17, 1922-1929.
Online |
| 434 |
C.M. Seubert, J. Stritzker, U. Donat, J.B. Sturm, N. Chen, J.M. von Hof, B. Krewer, L.F. Tietze, I. Gentschev, A.A. Szalay
|
Enhanced tumor therapy using vaccinia virus strain GLV-1h68 in combination with a β-galactosidase-activatable prodrug seco-analog of duocarmycin SA.
Cancer Gene Ther. 2011, 18, 42-52.
Online |
| 435 |
L.O.A. Manguro, J.O. Midiwo, L.F. Tietze, P. Hao
|
Triterpene saponins of Maesa lanceolata leaves.
Arkivoc 2011, 172-198.
Online
|
| 436 |
L.F. Tietze, M.A. Düfert, T. Hungerland, K. Oum, T. Lenzer
|
Synthesis and Photochemical Investigations of Tetrasubstituted Alkenes as Molecular Switches-The Effect of Substituents.
Chem. Eur. J. 2011, 17, 8452-8461.
Online
|
| 437 |
L.F. Tietze, K. Schmuck
|
SiFa Azide - A New Building Block for PET Imaging Using Click Chemistry.
Synlett 2011, 1697-1700.
Online
|
| 438 |
L.F. Tietze, S. Dietz, N. Böhnke, M. A. Düfert, I. Objartel, D. Stalke
|
Three-Component Domino Knoevenagel/Hetero-Diels-Alder Reaction for the Synthesis of the Amino Sugars 2-Acetoxyforosamine and 2-Acetoxyossamine - Experimental and Theoretical Results.
Eur. J. Org. Chem. 2011, 6574-6580.
Online
|
| 439 |
L.F. Tietze, K. Schmuck
|
Prodrugs for Targeted Tumor Therapies: Recent Developments in ADEPT, GDEPT and PMT.
Curr. Pharm. Des. 2011, 17, 3527-3547.
Online
|
| 440 |
J.E. Mathejczyk, J. Pauli, C. Dullin, J. Napp, L.F. Tietze, H. Kessler, U. Resch-Genger, F. Alves
|
Spectroscopically Well-Characterized RGD Optical Probe as a Prerequisite for Lifetime-Gated Tumor Imaging.
Molecular Imaging 2011, 10, 469-480.
Online
|
| 441 |
L.A. Pardo, D. Gomez-Varela, F. Major, K. Sansuk, R. Leurs, B.R. Downie, L.F. Tietze, W. Stühmer
|
Approaches Targeting KV10.1 Open a Novel Window for Cancer Diagnosis and Therapy.
Curr. Med. Chem. 2012, 19, 675-682.
Online
|
| 442 |
J.E. Rixson, T. Chaloner, C.H. Heath, L.F. Tietze, S.G. Stewart
|
The Development of Domino Reactions Incorporating the Heck Reaction: The Formation of N-Heterocycles.
Eur. J. Org. Chem. 2011, 544-558.
Online
|
| 443 |
L.F. Tietze, T. Hungerland, M.A. Düfert, I. Objartel, D. Stalke
|
Synthesis of tetra-substituted Alkenes through a Pd-catalyzed domino-Carbopalladation/CH-Activation.
Chem. Eur. J. 2012, 18, 3286-3291.
Online
|
| 444 |
T. Wirth, K. Schmuck, L.F. Tietze, S.A. Sieber |
Duocarmycin analogues target aldehyde dehydrogenase 1 in lung cancer cells.
Angew. Chem. 2012, 124, 2928-2931;
Angew. Chem., Int. Ed. 2012, 51, 2874-2877.
Online |
| 445 |
L.F. Tietze, T. Wolfram, J.J. Holstein, B. Dittrich |
First Enantioselective Total Synthesis of (+)-(R)-Pinnatolide Using an Asymmetric Domino Allylation Reaction.
Org. Lett. 2012, 14, 4035-4037.
Online |
| 446 |
L.F. Tietze, T. Hungerland, C. Depken, C.Maaß, D. Stalke |
Palladium-catalyzed Domino-Carbopalladation/CH-Activation for the Synthesis of Tetrasubstituted Alkenes bearing 5- and 7-membered Rings.
Synlett 2012, 2516-2520.
Online |
| 447 |
L.F. Tietze, N. Schützenmeister, A. Grube, T. Scheffer, M. M. Baag, M. Granitzka, D. Stalke |
Synthesis of Novel Spinosyn Analogues for Modern Crop Protection.
Eur. J. Org. Chem. 2012, 5748-5756.
Online |
| 448 |
T. Iven, S. König, S. Singh, S.A. Braus-Stromeyer, M. Bischoff, L.F. Tietze, G.H. Braus, V. Lipka, I. Feussner, Wolfgang Dröge-Laser |
Transcriptional Activation and Production of Tryptophan-Derived Secondary Metabolites in Arabidopsis Roots Contributes to the Defense against the Fungal Vascular Pathogen Verticillium longisporum.
Mol. Plant, 2012, 5, 1389-1402.
Online |
| 449 |
L.F. Tietze, M.A. Düfert, S.-C. Schild |
General Principles of Diastereoselective Reactions: Diastereoselective Domino Reactions.
In: Carreira E.M. and Yamamoto H. (eds.) Comprehensive Chirality, 2012, Volume 2, pp. 97-121. Amsterdam: Elsevier. |
| 450 |
L.F. Tietze, F. Behrendt, G.F. Pestel, I. Schuberth, M. Mitkovski |
Synthesis, Biological Evaluation and Live Cell Imaging of Novel Fluorescent Duocarmycin Analogues.
Chem. Biodiversity 2012, 2559-2570.
Online |
| 451 |
L.F. Tietze, A. Heins, J.R. Reiner, S.-C. Duefert, I. Schuberth |
Synthesis and Biological Evaluation of a Novel Acronycine/Duocarmycin Hybrid Natural Product.
Heterocycles 2012, 425-433.
Online |
| 452 |
L.F. Tietze, S.G. Stewart, A. Düfert |
Domino Reactions in the Enantioselective Synthesis of Bioactive Natural Products in
"Modern Tools for the Synthesis of Complex Bioactive Molecules" (Ed.: J. Cossy, S. Arseniyadis)
John Wiley & Sons, 2012, p. 271-334 (ISBN-13: 978-0470616185). |
| 453 |
L.F. Tietze, M. Müller, S.-C. Duefert, K. Schmuck, I. Schuberth |
Photoactivatable Prodrugs of Highly Potent Duocarmycin Analogues for a Selective Cancer Therapy.
Chem. Eur. J. 2013, 19, 1726-1731.
Online |
| 454 |
L.F. Tietze, S.-C. Duefert, J. Clerc, M. Bischoff, C. Maaß, D. Stalke |
Total Synthesis of Linoxepin through a Palladium-Catalyzed Domino Reaction.
Angew. Chem. 2013, 125, 3273-3276;
Angew. Chem., Int. Ed. 2013, 52, 3191-3194.
Online |
| 455 |
L.F. Tietze, T. Hungerland, C. Eichhorst, A. Düfert, C. Maaß, D. Stalke |
Efficient Synthesis of Helical Tetrasubstituted Alkenes as Potential Molecular Switches: A Two-Component Palladium-Catalyzed Triple Domino Process.
Angew. Chem. 2013, 125, 3756-3759;
Angew. Chem., Int. Ed. 2013, 52, 3668-3671.
Online |
| 456 |
L.F. Tietze, S. Jackenkroll, C. Raith, D.A. Spiegl, J.R. Reiner, M.C. Ochoa Campos |
Enantioselective Total Synthesis of (-)-Diversonol.
Chem. Eur. J. 2013, 19, 4876-4882.
Online |
| 457 |
L.F. Tietze, S.A. Sieber |
Duocarmycin Analogues without a DNA-Binding Indole Unit Associate with Aldehyde Dehydrogenase 1A1 and not DNA: A Reply.
Angew. Chem. 2013, 125, 5557-5559;
Angew. Chem., Int. Ed. 2013, 52, 5447-5449.
Online |
| 458 |
L.F. Tietze, L. Ma, J.R. Reiner, S. Jackenkroll, S. Heidemann |
Enantioselective Total Synthesis of (-)-Blennolide A.
Chem. Eur. J. 2013, 19, 8610-8614.
Online |
| 459 |
T. Wirth, G.F. Pestel, V. Ganal, T. Kirmeier, I. Schuberth, T. Rein, L.F. Tietze, S.A. Sieber |
The Two Faces of Potent Antitumor Duocarmycin-Based Drugs: A Structural Dissection Reveals Disparate Motifs for DNA versus Aldehyde Dehydrogenase 1 Affinity.
Angew. Chem. 2013, 125, 7059-7063;
Angew. Chem., Int. Ed. 2013, 52, 6921-6925.
Online |
| 460 |
L.F. Tietze, S. Dietz, N. Schützenmeister, S. Biller, J. Hierold, T. Scheffer, M.M. Baag |
Selective Glycosylation with the Amino Sugar D-Forosamine for the Synthesis of Spinosyns and Its Analogues.
Eur. J. Org. Chem. 2013, 7305-7312.
Online |
| 461 |
L.F. Tietze, T. Hungerland, J. Ammermann, C. Eichhorst, S.O. Reichmann, D. Stalke |
A facile synthesis of 3-substituted benzofurans and indoles through a palladium-catalyzed domino carbopalladation/CH-activation/isomerization process.
Ind. Chem. Soc. 2013, 90, 1537-1555.
|
| 462 |
K.-C. Chen, K. Schmuck, L.F. Tietze, S.R. Roffler |
Selective Cancer Therapy by Extracellular Activation of a Highly Potent Glycosidic Duocarmycin Analogue.
Mol. Pharmaceutics 2013, 10, 1773-1782.
Online
|
| 463 |
L.F. Tietze, L. Ma, S. Jackenkroll, J.R. Reiner, J. Hierold, B. Gnanaprakasam, S. Heidemann |
The Paecilin Puzzle - Enantioselective Synthesis of the Proposed Structures of Paecilin A and B.
Heterocycles 2014, 88, 1101-1119.
Online |
| 464 |
L.F. Tietze, S.-C. Düfert, J. Hierold |
Domino Reactions in the Total Synthesis of Natural Products in "Domino Reactions: Concepts for Efficient Organic Synthesis" (Ed.: L.F. Tietze) Wiley-VCH, Weinheim,
2014, p. 523-578.
|
| 465 |
L.F. Tietze, S. Jackenkroll, J. Hierold, L. Ma, B. Waldecker |
A Domino Approach to the Enantioselective Total Syntheses of Blennolide C and Gonytolide C. Chem. Eur. J.
2014, 20, 8628-8635.
Online
|
| 466 |
L.F. Tietze, C. Eichhorst, T. Hungerland, M. Steinert |
A Fast Way to Fluorescence: A Fourfold Domino Reaction to Condensed Polycyclic Compounds.
Chem. Eur. J. 2014, 20, 12553-12558.
Online |
| 467 |
L.F. Tietze, J. Clerc, S. Biller, S.-C. Duefert, M. Bischoff |
Enantioselective Total Synthesis of the Lignan (+)-Linoxepin.
Chem. Eur. J. 2014, 20, 17119-17124.
Online |
| 468 |
L.F. Tietze, C. Eichhorst |
An efficient Domino Sonogashira/double Carbopalladation/C-H-Activation Reaction leading to Fluorescent Polycyclic Aromatic Hydrocarbons. Heterocycles
2015, 90, 919-927.
Online
|
| 469 |
L.F. Tietze, T. Eicher, U. Diederichsen, A. Speicher, N. Schützenmeister |
Reactions and Syntheses in the Organic Chemistry Laboratory, 2nd Edition (completely revised and updated), Wiley-VCH, Weinheim, 2015.
|
| 470 |
L.F. Tietze, B. Waldecker, D. Ganapathy, C. Eichhorst, T. Lenzer, K. Oum, S.O. Reichmann, D. Stalke |
Four-and Sixfold Tandem-Domino Reactions Leading to Dimeric Tetrasubstituted Alkenes Suitable as Molecular Switches.
Angew. Chem. 2015, 127, 10457-10461;
Angew. Chem., Int. Ed. 2015, 54, 10317-10321.
Online |
| 471 |
M.F. Koch, S. Harteis, I.D. Blank, G. Pestel, L.F. Tietze, C. Ochsenfeld, S. Schneider and S.A. Sieber |
Structural, Biochemical, and Computational Studies Reveal the Mechanism of SelectiveAldehydeDehydrogenase 1A1 Inhibitionby Cytotoxic Duocarmycin Analogues.
Angew. Chem. 2015, 127, 13754-13758;
Angew. Chem., Int. Ed. 2015, 54, 13550-13554.
Online |
| 472 |
J. Hierold, S. Baek, R. Rieger, T.-G. Lim, S. Zakpur, M. Arciniega, K.W. Lee, R. Huber, L.F. Tietze |
Design, Synthesis, and Biological Evaluation of Quercetagetin Analogues as JNK1 Inhibitors.
Chem. Eur. J. 2015, 21, 16887-16894.
Online |
| 473 |
D. Ganapathy, J.R. Reiner, L.E. Löffler, L. Ma, B. Gnanaprakasam, B. Niepötter, I. Koehne, L.F. Tietze |
Enantioselective Total Synthesis of Secalonic Acid E.
Chem. Eur. J. 2015, 21, 16807-16810.
Online |
| 479 |
R. Gandamala, S. Hoekman, M. Kangani, J. E. Nidhiry, K. Penchalaiah, D. Singh, L. F. Tietze |
Synthesis and Biology of Dimeric, Trimeric and Tetrameric Analogues of Duocarmycin SA.
Heterocycles 2018, 97, 260-272.
Online |
| 480 |
T. A. Khan, T. Fornefeld, D.Hübner, P. Vana, L. F. Tietze |
Palladium-Catalyzed Fourfold Domino Reaction for the Synthesis of a Polymeric Double Switch.
, Org. Lett. 2018, 20, 2007-2010.
Online |
| 481 |
S. Senthilkumar, G. Valdomir , D. Ganapathy, Y. Zhang, L. F. Tietze |
Enantioselective Total Synthesis of the Fungal Metabolite Blennolide D and the Enantiomers of Blennolide E and F.
, Org. Lett. 2018, 20, 2186-2189.
Online |
| 482 |
G. Valdomir, S. Senthilkumar, D. Ganapathy, Y. Zhang, L. F. Tietze |
Enantioselective Total Synthesis of Blennolide H and Phomopsis-H76 A and Determination of Their Structure
, Chem. Eur. J. 2018, 24, 8760-8763.
Online |
| 483 |
G. Valdomir, S. Senthilkumar, D. Ganapathy, Y. Zhang, L. F. Tietze |
Enantioselective Total Synthesis of Chromanone Lactone Homo- and Heterodimers.
, Chem. Asian J. 2018, 13, 1888-1891.
Online |
| 484 |
F. Lotz, K. Kahle, M. Kangani, S. Senthil Kumar, L. F. Tietze |
Domino C-H Activation Reactions through Proximity Effects.
, Eur. J. Org. Chem. 2018, 5562-5569.
Online |
Publikationen 2006