Lutz Friedjan Tietze - Publications

Affiliations: 
Organic chemistry Georg-August-Universität Göttingen, Göttingen, Niedersachsen, Germany 
Area:
Natural products chemistry
Website:
http://www.tietze.chemie.uni-goettingen.de/elebensl.php

192 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Tietze LF, Jackenkroll S, Ganapathy D, Reiner JR. Formal Synthesis of (-)-Siccanin Using an Enantioselective Domino Wacker/Carbonylation/Methoxylation Reaction Synlett. 27: 96-100. DOI: 10.1055/s-0035-1560752  0.6
2015 Hierold J, Baek S, Rieger R, Lim TG, Zakpur S, Arciniega M, Lee KW, Huber R, Tietze LF. Design, Synthesis, and Biological Evaluation of Quercetagetin Analogues as JNK1 Inhibitors. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 16887-94. PMID 26541354 DOI: 10.1002/chem.201502475  0.6
2015 Ganapathy D, Reiner JR, Löffler LE, Ma L, Gnanaprakasam B, Niepötter B, Koehne I, Tietze LF. Enantioselective Total Synthesis of Secalonic Acid E. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 16807-10. PMID 26447631 DOI: 10.1002/chem.201503593  0.6
2015 Koch MF, Harteis S, Blank ID, Pestel G, Tietze LF, Ochsenfeld C, Schneider S, Sieber SA. Structural, Biochemical, and Computational Studies Reveal the Mechanism of Selective Aldehyde Dehydrogenase 1A1 Inhibition by Cytotoxic Duocarmycin Analogues. Angewandte Chemie (International Ed. in English). PMID 26373694 DOI: 10.1002/anie.201505749  0.6
2015 Tietze LF, Eichhorst C. An efficient domino Sonogashira/double carbopalladation/C-H-activation reaction leading to fluorescent polycyclic aromatic hydrocarbons Heterocycles. 90: 919-927. DOI: 10.3987/COM-14-S(K)39  0.6
2015 Tietze LF, Waldecker B, Ganapathy D, Eichhorst C, Lenzer T, Oum K, Reichmann SO, Stalke D. Four- and Sixfold Tandem-Domino Reactions Leading to Dimeric Tetrasubstituted Alkenes Suitable as Molecular Switches Angewandte Chemie - International Edition. DOI: 10.1002/anie.201503538  0.6
2014 Tietze LF, Eichhorst C, Hungerland T, Steinert M. A fast way to fluorescence: a fourfold domino reaction to condensed polycyclic compounds Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 12553-12558. PMID 25112207 DOI: 10.1002/chem.201402961  0.6
2014 Tietze LF, Jackenkroll S, Hierold J, Ma L, Waldecker B. A domino approach to the enantioselective total syntheses of blennolide C and gonytolide C Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 8628-8635. PMID 24905446 DOI: 10.1002/chem.201402495  0.6
2014 Tietze LF, Ma L, Jackenkroll S, Reiner JR, Hierold J, Gnanaprakasam B, Heidemann S. The paecilin puzzle - Enantioselective syntheses of the proposed structures of paecilin A and B Heterocycles. 88: 1101-1119. DOI: 10.3987/COM-13-S(S)68  0.6
2014 Tietze LF, Clerc J, Biller S, Duefert SC, Bischoff M. Enantioselective total synthesis of the lignan (+)-Linoxepin Chemistry - a European Journal. 20: 17119-17124. DOI: 10.1002/chem.201404679  0.6
2013 Wirth T, Pestel GF, Ganal V, Kirmeier T, Schuberth I, Rein T, Tietze LF, Sieber SA. The two faces of potent antitumor duocarmycin-based drugs: A structural dissection reveals disparate motifs for DNA versus aldehyde dehydrogenase 1 affinity Angewandte Chemie - International Edition. 52: 6921-6925. PMID 23681547 DOI: 10.1002/anie.201208941  0.6
2013 Tietze LF, Ma L, Reiner JR, Jackenkroll S, Heidemann S. Enantioselective total synthesis of (-)-blennolide A Chemistry - a European Journal. 19: 8610-8614. PMID 23649592 DOI: 10.1002/chem.201300479  0.6
2013 Tietze LF, Sieber SA. Duocarmycin analogues without a DNA-binding indole unit associate with aldehyde dehydrogenase1A1 and not DNA: A reply Angewandte Chemie - International Edition. 52: 5447-5449. PMID 23616344 DOI: 10.1002/anie.201301923  0.6
2013 Tietze LF, Jackenkroll S, Raith C, Spiegl DA, Reiner JR, Ochoa Campos MC. Enantioselective total synthesis of (-)-diversonol Chemistry - a European Journal. 19: 4876-4882. PMID 23417866 DOI: 10.1002/chem.201204037  0.6
2013 Tietze LF, Duefert SC, Clerc J, Bischoff M, Maaß C, Stalke D. Total synthesis of linoxepin through a palladium-catalyzed domino reaction Angewandte Chemie - International Edition. 52: 3191-3194. PMID 23404683 DOI: 10.1002/anie.201209868  0.6
2013 Tietze LF, Müller M, Duefert SC, Schmuck K, Schuberth I. Photoactivatable prodrugs of highly potent duocarmycin analogues for a selective cancer therapy Chemistry - a European Journal. 19: 1726-1731. PMID 23225610 DOI: 10.1002/chem.201202773  0.6
2013 Chen KC, Schmuck K, Tietze LF, Roffler SR. Selective cancer therapy by extracellular activation of a highly potent glycosidic duocarmycin analogue Molecular Pharmaceutics. 10: 1773-1782. DOI: 10.1021/mp300581u  0.6
2013 Tietze LF, Dietz S, Schützenmeister N, Biller S, Hierold J, Scheffer T, Baag MM. Selective glycosylation with the amino sugar D-forosamine for the synthesis of spinosyns and its analogues European Journal of Organic Chemistry. 7305-7312. DOI: 10.1002/ejoc.201300983  0.6
2013 Tietze LF, Hungerland T, Eichhorst C, Düfert A, Maaß C, Stalke D. Efficient synthesis of helical tetrasubstituted alkenes as potential molecular switches: A two-component palladium-catalyzed triple domino process Angewandte Chemie - International Edition. 52: 3668-3671. DOI: 10.1002/anie.201209510  0.6
2013 Tietze LF, Hungerland T, Ammermann J, Eichhorst C, Reichmann SO, Stalke D. A facile synthesis of 3-substituted benzofurans and indoles through a palladium-catalyzed domino carbopalladation/CH-activation/isomerization process Journal of the Indian Chemical Society. 90: 1537-1555.  0.6
2012 Tietze LF, Behrendt F, Pestel GF, Schuberth I, Mitkovski M. Synthesis, biological evaluation, and live cell imaging of novel fluorescent duocarmycin analogs Chemistry and Biodiversity. 9: 2559-2570. PMID 23161634 DOI: 10.1002/cbdv.201200289  0.6
2012 Tietze LF, Wolfram T, Holstein JJ, Dittrich B. First enantioselective total synthesis of (+)-(R)-pinnatolide using an asymmetric domino allylation reaction Organic Letters. 14: 4035-4037. PMID 22853329 DOI: 10.1021/ol301932d  0.6
2012 Iven T, König S, Singh S, Braus-Stromeyer SA, Bischoff M, Tietze LF, Braus GH, Lipka V, Feussner I, Dröge-Laser W. Transcriptional activation and production of tryptophan-derived secondary metabolites in arabidopsis roots contributes to the defense against the fungal vascular pathogen verticillium longisporum Molecular Plant. 5: 1389-1402. PMID 22522512 DOI: 10.1093/mp/sss044  0.6
2012 Wirth T, Schmuck K, Tietze LF, Sieber SA. Duocarmycin analogues target aldehyde dehydrogenase 1 in lung cancer cells Angewandte Chemie - International Edition. 51: 2874-2877. PMID 22334487 DOI: 10.1002/anie.201106334  0.6
2012 Tietze LF, Hungerland T, Düfert A, Objartel I, Stalke D. Synthesis of tetrasubstituted alkenes through a palladium-catalyzed domino carbopalladation/C-H-activation reaction Chemistry - a European Journal. 18: 3286-3291. PMID 22259072 DOI: 10.1002/chem.201103209  0.6
2012 Pardo LA, Gómez-Varela D, Major F, Sansuk K, Leurs R, Downie BR, Tietze LF, Stühmer W. Approaches targeting K(V)10.1 open a novel window for cancer diagnosis and therapy. Current Medicinal Chemistry. 19: 675-82. PMID 22204340 DOI: 10.2174/092986712798992011  0.6
2012 Tietze LF, Heins A, Reiner JR, Duefert SC, Schuberth I. Synthesis and biological evaluation of a novel acronycine/duocarmycin hybrid natural product Heterocycles. 86: 425-433. DOI: 10.3987/COM-12-S(N)37  0.6
2012 Tietze LF, Hungerland T, Depken C, Maaß C, Stalke D. Palladium-catalyzed domino carbopalladation/C-H activation for the synthesis of tetrasubstituted alkenes bearing five- and seven-membered rings Synlett. 23: 2516-2520. DOI: 10.1055/s-0032-1317325  0.6
2012 Tietze LF, Düfert MA, Schild SC. 2.5 General Principles of Diastereoselective Reactions: Diastereoselective Domino Reactions Comprehensive Chirality. 2: 97-121. DOI: 10.1016/B978-0-08-095167-6.00206-8  0.6
2012 Tietze LF, Schützenmeister N, Grube A, Scheffer T, Baag MM, Granitzka M, Stalke D. Synthesis of spinosyn analogues for modern crop protection European Journal of Organic Chemistry. 5748-5756. DOI: 10.1002/ejoc.201200600  0.6
2012 Rixson JE, Chaloner T, Heath CH, Tietze LF, Stewart SG. The development of domino reactions incorporating the heck reaction: The formation of N-heterocycles European Journal of Organic Chemistry. 544-558. DOI: 10.1002/ejoc.201101305  0.6
2012 Tietze LF, Stewart SG, Düfert A. Domino Reactions in the Enantioselective Synthesis of Bioactive Natural Products Modern Tools For the Synthesis of Complex Bioactive Molecules. 271-334. DOI: 10.1002/9781118342886.ch9  0.6
2011 Mathejczyk JE, Pauli J, Dullin C, Napp J, Tietze LF, Kessler H, Resch-Genger U, Alves F. Spectroscopically well-characterized RGD optical probe as a prerequisite for lifetime-gated tumor imaging Molecular Imaging. 10: 469-480. PMID 22201538 DOI: 10.2310/7290.2011.00018  0.6
2011 Tietze LF, Schmuck K. Prodrugs for targeted tumor therapies: Recent developments in ADEPT, GDEPT and PMT Current Pharmaceutical Design. 17: 3527-3547. PMID 22074425 DOI: 10.2174/138161211798194459  0.6
2011 Tietze LF, Schmuck K, Schuster HJ, Müller M, Schuberth I. Synthesis and biological evaluation of prodrugs based on the natural antibiotic duocarmycin for use in ADEPT and PMT Chemistry - a European Journal. 17: 1922-1929. PMID 21274943 DOI: 10.1002/chem.201002798  0.6
2011 Seubert CM, Stritzker J, Hess M, Donat U, Sturm JB, Chen N, Hof JMV, Krewer B, Tietze LF, Gentschev I, Szalay AA. Enhanced tumor therapy using vaccinia virus strain GLV-1h68 in combination with a Β-galactosidase-activatable prodrug seco-analog of duocarmycin SA Cancer Gene Therapy. 18: 42-52. PMID 20829890 DOI: 10.1038/cgt.2010.49  0.6
2011 Tietze LF, Schmuck K. SiFA azide: A new building block for PET imaging using click chemistry Synlett. 1697-1700. DOI: 10.1055/s-0030-1260942  0.6
2011 Tietze LF, Dietz S, Böhnke N, Düfert MA, Objartel I, Stalke D. Three-component domino knoevenagel/hetero-diels-alder reaction for the synthesis of the amino sugars 2-acetoxyforosamine and 2-acetoxyossamine- experimental and theoretical results European Journal of Organic Chemistry. 6574-6580. DOI: 10.1002/ejoc.201100725  0.6
2011 Tietze LF, Düfert MA, Hungerland T, Oum K, Lenzer T. Synthesis and photochemical investigations of tetrasubstituted alkenes as molecular switches-the effect of substituents Chemistry - a European Journal. 17: 8452-8461. DOI: 10.1002/chem.201003559  0.6
2011 Manguro LOA, Midiwo JO, Tietze LF, Hao P. Triterpene saponins of Maesa lanceolata leaves Arkivoc. 2011: 172-198.  0.6
2010 Tietze LF, Schuster HJ, von Hof JM, Hampel SM, Colunga JF, John M. Atropisomerism of aromatic carbamates. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 12678-82. PMID 20886469 DOI: 10.1002/chem.201001047  0.6
2010 Tietze LF, Von Hof JM, Müller M, Krewer B, Schuberth I. Glycosidic prodrugs of highly potent bifunctional duocarmycin derivatives for selective treatment of cancer Angewandte Chemie - International Edition. 49: 7336-7339. PMID 20799305 DOI: 10.1002/anie.201002502  0.6
2010 Schuster HJ, Krewer B, Von Hof JM, Schmuck K, Schuberth I, Alves F, Tietze LF. Synthesis of the first spacer containing prodrug of a duocarmycin analogue and determination of its biological activity Organic and Biomolecular Chemistry. 8: 1833-1842. PMID 20449487 DOI: 10.1039/b925070k  0.6
2010 Schubert M, Melnikova AN, Mesecke N, Zubkova EK, Fortte R, Batashev DR, Barth I, Sauer N, Gamalei YV, Mamushina NS, Tietze LF, Voitsekhovskaja OV, Pawlowski K. Two novel disaccharides, rutinose and methylrutinose, are involved in carbon metabolism in Datisca glomerata Planta. 231: 507-521. PMID 19915863 DOI: 10.1007/s00425-009-1049-5  0.6
2010 Bajohr LL, Ma L, Platte C, Liesenfeld O, Tietze LF, Groß U, Bohne W. In vitro and in vivo activities of 1-hydroxy-2-alkyl-4(1H)quinolone derivatives against toxoplasma gondii Antimicrobial Agents and Chemotherapy. 54: 517-521. PMID 19884369 DOI: 10.1128/AAC.01001-09  0.6
2010 Tietze LF, Ma L. Synthesis of novel 1-hydroxyquinolones with high anti-toxoplasma activity Heterocycles. 82: 377-396. DOI: 10.3987/COM-10-S(E)9  0.6
2010 Tietze LF, Düfert A. Multiple Pd-catalyzed reactions in the synthesis of natural products, drugs, and materials Pure and Applied Chemistry. 82: 1375-1392. DOI: 10.1351/PAC-CON-09-12-10  0.6
2010 Tietze LF, Biller S, Wolfram T. 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. 2130-2132. DOI: 10.1055/s-0030-1258537  0.6
2010 Tietze LF, Behrendt F, Major F, Krewer B, Von Hof JM. Synthesis of fluorescence-labelled glycosidic prodrugs based on the cytotoxic antibiotic duocarmycin European Journal of Organic Chemistry. 6909-6921. DOI: 10.1002/ejoc.201000966  0.6
2010 Tietze LF, Schuster HJ, Von Hof JM, Hampel SM, Colunga JF, John M. Atropisomerism of aromatic carbamates Chemistry - a European Journal. 16: 12678-12682. DOI: 10.1002/chem.201001047  0.6
2010 Tietze LF, Düfert A. Domino Reactions Involving Catalytic Enantioselective Conjugate Additions Catalytic Asymmetric Conjugate Reactions. 321-350. DOI: 10.1002/9783527630578.ch8  0.6
2009 Tietze LF, Düfert A, Lotz F, Sölter L, Oum K, Lenzer T, Beck T, Herbst-Irmer R. Synthesis of chiroptical molecular switches by pd-catalyzed domino reactions. Journal of the American Chemical Society. 131: 17879-84. PMID 19911798 DOI: 10.1021/ja906260x  0.6
2009 Tietze LF, Tolle N, Kratzert D, Stalke D. Efficient formal total synthesis of the erythrina alkaloid (+)-erysotramidine, using a domino process Organic Letters. 11: 5230-5233. PMID 19860384 DOI: 10.1021/ol901980u  0.6
2009 Tietze LF, Krewer B, Major F, Schuberth I. CD-spectroscopy as a powerful tool for investigating the mode of action of unmodified drugs in live cells Journal of the American Chemical Society. 131: 13031-13036. PMID 19697908 DOI: 10.1021/ja902767f  0.6
2009 Tietze LF, Krewer B, Frauendorf H. Probing the mechanism of action of potential anticancer agents at a molecular level using electrospray ionisation Fourier transform ion cyclotron resonance mass spectrometry European Journal of Mass Spectrometry. 15: 661-672. PMID 19679946 DOI: 10.1255/ejms.1021  0.6
2009 Tietze LF, Krewer B. Antibody-directed enzyme prodrug therapy: A promising approach for a selective treatment of cancer based on prodrugs and monoclonal antibodies Chemical Biology and Drug Design. 74: 205-211. PMID 19660031 DOI: 10.1111/j.1747-0285.2009.00856.x  0.6
2009 Tietze LF, Krewer B, Frauendorf H. Investigation of the transformations of a novel anti-cancer agent combining HPLC, HPLC-MS and direct ESI-HRMS analyses Analytical and Bioanalytical Chemistry. 395: 437-448. PMID 19641906 DOI: 10.1007/s00216-009-2963-x  0.6
2009 Dullin C, Zientkowska M, Napp J, Missbach-Guentner J, Krell HW, Muller F, Grabbe E, Tietze LF, Alves F. Semiautomatic landmark-based two-dimensional three-dimensional image fusion in living mice: correlation of near-infrared fluorescence imaging of cy5.5-labeled antibodies with flat-panel volume computed tomography Molecular Imaging. 8: 2-14. PMID 19344571 DOI: 10.2310/7290.2009.00001  0.6
2009 Alves F, Dullin C, Napp J, Missbach-Guentner J, Jannasch K, Mathejczyk J, Pardo LA, Stühmer W, Tietze LF. Concept of a selective tumour therapy and its evaluation by near-infrared fluorescence imaging and flat-panel volume computed tomography in mice. European Journal of Radiology. 70: 286-93. PMID 19285818 DOI: 10.1016/j.ejrad.2009.01.048  0.6
2009 Tietze LF, Krewer B. Novel analogues of CC-1065 and the duocarmycins for the use in targeted tumour therapies Anti-Cancer Agents in Medicinal Chemistry. 9: 304-325. PMID 19275523  0.6
2009 Tietze LF, Schuster HJ, Krewer B, Schuberth I. Synthesis and biological studies of different duocarmycin based glycosidic prodrugs for their use in the antibody-directed enzyme prodrug therapy. Journal of Medicinal Chemistry. 52: 537-543. PMID 19143570 DOI: 10.1021/jm8009102  0.6
2009 Islam KMD, Dilcher M, Thurow C, Vock C, Krimmelbein IK, Tietze LF, Gonzalez V, Zhao H, Gatz C. Directed evolution of estrogen receptor proteins with altered ligand-binding specificities Protein Engineering, Design and Selection. 22: 45-52. PMID 19088113 DOI: 10.1093/protein/gzn067  0.6
2009 Tietze LF, Heins A, Soleiman-Beigi M, Raith C. Synthesis of annulated 1,4-dioxanes and perhydro-1,4-oxazines by domino-wacker-carbonylation and domino-wacker-mizoroki-heck reactions Heterocycles. 77: 1123-1146. DOI: 10.3987/COM-08-S(F)91  0.6
2009 Tietze LF, Vock CA, Krimmelbein IK, Nacke L. Synthesis of novel structurally simplified estrogen analogues with electron-donating groups in ring A Synthesis. 2040-2060. DOI: 10.1055/s-0029-1216810  0.6
2009 Tietze LF, Kinzel T, Wolfram T. Asymmetrie allylation of methyl ketones by using chiral phenyl carbinols Chemistry - a European Journal. 15: 6199-6210. DOI: 10.1002/chem.200900062  0.6
2009 Tietze LF, Kinzel T, Schmatz S. Stereoselective allylation of ketones: Explanation for the unusual inversion of the induced stereochemistry in the auxiliary-mediated crotylation and pentenylation of butanone by DFT calculations Chemistry - a European Journal. 15: 1706-1712. DOI: 10.1002/chem.200801889  0.6
2009 Tietze LF, Levy LM. The Mizoroki-Heck Reaction in Domino Processes The Mizoroki-Heck Reaction. 281-344. DOI: 10.1002/9780470716076.ch8  0.6
2009 Opiyo SA, Ogur JA, Manguro LOA, Tietze LF, Schuster H. A new sterol diglycoside from conyza floribunda South African Journal of Chemistry. 62: 163-167.  0.6
2008 Tietze LF, Von Hof JM, Krewer B, Müller M, Major F, Schuster HJ, Schuberth I, Alves F. Asymmetric synthesis and biological evaluation of glycosidic prodrugs for a selective cancer therapy Chemmedchem. 3: 1946-1955. PMID 19021160 DOI: 10.1002/cmdc.200800250  0.6
2008 Tietze LF, Spiegl DA, Stecker F, Major J, Raith C, Große C. Stereoselective synthesis of 4-dehydroxydiversonol employing enantioselective palladium-catalysed domino reactions Chemistry - a European Journal. 14: 8956-8963. PMID 18698572 DOI: 10.1002/chem.200800967  0.6
2008 Tietze LF, Brazel CC, Hölsken S, Magull J, Ringe A. Total synthesis of polyoxygenated cembrenes Angewandte Chemie - International Edition. 47: 5246-5249. PMID 18528838 DOI: 10.1002/anie.200800626  0.6
2008 Tietze LF, Schuster HJ, Schmuck K, Schuberth I, Alves F. Duocarmycin-based prodrugs for cancer prodrug monotherapy Bioorganic and Medicinal Chemistry. 16: 6312-6318. PMID 18524605 DOI: 10.1016/j.bmc.2008.05.009  0.6
2008 Tietze LF, Kinzel T, Schmatz S. 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 Journal of the American Chemical Society. 130: 4386-4395. PMID 18331031 DOI: 10.1021/ja078032a  0.6
2008 Tietze LF, Vock CA, Krimmelbein IK, Wiegand JM, Nacke L, Ramachandar T, Islam KM, Gatz C. Synthesis of novel structurally simplified estrogen analogues. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 3670-9. PMID 18327882 DOI: 10.1002/chem.200701600  0.6
2008 Tietze LF, Panknin O, Major F, Krewer B. Synthesis of a novel pentagastrin-drug conjugate for a targeted tumor therapy. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 2811-2818. PMID 18214880 DOI: 10.1002/chem.200701521  0.6
2008 Tietze LF, Redert T, Bell HP, Hellkamp S, Levy LM. Efficient synthesis of the structural core of tetracyclines by a palladium-catalyzed domino Tsuji-Trost-Heck-Mizoroki reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 2527-35. PMID 18200642 DOI: 10.1002/chem.200701676  0.6
2008 Tietze LF, Krimmelbein IK. Enantioselective total synthesis of the oral contraceptive desogestrel by a double Heck reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 1541-1551. PMID 18038382 DOI: 10.1002/chem.200700182  0.6
2008 Tietze LF, Schuster HJ, Hampel SM, Rühl S, Pfoh R. Enantio- And diastereoselective synthesis of duocarmycine-based prodrugs for a selective treatment of cancer by epoxide opening Chemistry - a European Journal. 14: 895-901. PMID 18033701 DOI: 10.1002/chem.200700988  0.6
2008 Tietze LF, Panknin O, Krewer B, Major F, Schuberth I. Synthesis and biological evaluation of a novel pentagastrin-toxin conjugate designed for a targeted prodrug monotherapy of cancer International Journal of Molecular Sciences. 9: 821-837. DOI: 10.3390/ijms9050821  0.6
2008 Tietze LF, Tölle N, Noll C. Highly efficient domino reaction for the synthesis of the erythrina and B-homoerythrina alkaloid skeleton Synlett. 525-528. DOI: 10.1055/s-2008-1032091  0.6
2008 Tietze LF, Raith C, Brazel CC, Hölsken S, Magull J. Enantioselective synthesis of 2-substituted alcohols using (+)-(1S,2S)-pseudoephedrine as chiral auxiliary Synthesis. 229-236. DOI: 10.1055/s-2008-1000851  0.6
2008 Werz DB, Schuster HJ, Tietze LF. Fast and efficient preparation of an α-fucosyl building block by reductive 1,2-benzylidene ring-opening reaction Synlett. 1969-1972. DOI: 10.1055/8-2008-1077961  0.6
2008 Elghamry I, Tietze LF. Microwave assisted synthesis of novel annealed porphyrins Tetrahedron Letters. 49: 3972-3975. DOI: 10.1016/j.tetlet.2008.04.094  0.6
2008 Tietze LF, Liu D. Continuous-flow microreactor multi-step synthesis of an aminonaphthalene derivative as starting material for the preparation of novel anticancer agents Arkivoc. 2008: 193-210.  0.6
2007 Tietze LF, Singidi RR, Gericke KM. Total synthesis of the proposed structure of the anthrapyran metabolite δ-indomycinone Chemistry - a European Journal. 13: 9939-9947. PMID 17886848 DOI: 10.1002/chem.200700823  0.6
2007 Tietze LF, Brasche G, Grube A, Böhnke N, Stadler C. Synthesis of novel spinosyn a analogues by Pd-mediated transformations Chemistry - a European Journal. 13: 8543-8563. PMID 17654624 DOI: 10.1002/chem.200700464  0.6
2007 Tietze LF, Major F, Schuberth I, Spiegl DA, Krewer B, Maksimenka K, Bringmann G, Magull J. Selective treatment of cancer: Synthesis, biological evaluation and structural elucidation of novel analogues of the antibiotic CC-1065 and the duocarmycins Chemistry - a European Journal. 13: 4396-4409. PMID 17455190 DOI: 10.1002/chem.200700113  0.6
2007 Tietze LF, Gericke KM, Singidi RR, Schuberth I. Novel strategies for the synthesis of anthrapyran antibiotics: Discovery of a new antitumor agent and total synthesis of (S)-espicufolin Organic and Biomolecular Chemistry. 5: 1191-1200. PMID 17406717 DOI: 10.1039/b700838d  0.6
2007 Tietze LF, Kinzel T. Synthesis of natural products and analogs using multiple Pd-catalyzed transformations Pure and Applied Chemistry. 79: 629-650. DOI: 10.1351/pac200779040629  0.6
2007 Tietze LF, Stadler C, Böhnke N, Brasche G, Grube A. Synthesis of enantiomerically pure cyclopentene building blocks Synlett. 485-487. DOI: 10.1055/s-2007-967937  0.6
2007 Tietze LF, Braun H, Steck PL, El Bialy SAA, Tölle N, Düfert A. Efficient synthesis of cephalotaxine- and deoxyharringtonine analogues by a trimethylaluminium-mediated domino reaction Tetrahedron. 63: 6437-6445. DOI: 10.1016/j.tet.2007.03.020  0.6
2007 Tietze LF, Singidi RR, Gericke KM, Böckemeier H, Laatsch H. Isolation, enantioselective total synthesis and structure determination of the anthrapyran metabolite SS 43405-e European Journal of Organic Chemistry. 5876-5878. DOI: 10.1002/ejoc.200700534  0.6
2007 Tietze LF, Gericke KM, Schuberth I. Synthesis of highly functionalized anthraquinones and evaluation of their antitumor activity European Journal of Organic Chemistry. 4563-4577. DOI: 10.1002/ejoc.200700418  0.6
2007 Tietze LF, Steck PL. High Pressure in Organic Synthesis: Influence on Selectivity High Pressure Chemistry: Synthetic, Mechanistic, and Supercritical Applications. 239-283. DOI: 10.1002/9783527612628.ch08  0.6
2007 Tietze LF, Zinngrebe J, Spiegl DA, Stecker F. Palladium-catalyzed domino-wacker-carbonylation reaction for the enantioselective synthesis of chromans and benzodioxins Heterocycles. 74: 473-489.  0.6
2007 Tietze LF, Böhnke N, Brasche G. Preparation of (2R)-2-acetoxy-D-forosamine for the total synthesis of spinosyns Arkivoc. 2007: 12-21.  0.6
2006 Tietze LF, Singidi RR, Gericke KM. First enantioselective total synthesis and structure determination of the anthrapyran metabolite gamma-indomycinone. Organic Letters. 8: 5873-6. PMID 17134294 DOI: 10.1021/ol062492b  0.6
2006 Tietze LF, Gericke KM, Singidi RR. Enantioselective total synthesis and structure determination of the antiherpetic anthrapyran antibiotic AH-1763 IIa. Angewandte Chemie (International Ed. in English). 45: 6990-3. PMID 17009355 DOI: 10.1002/anie.200601992  0.6
2006 Tietze LF, Stecker F, Zinngrebe J, Sommer KM. Enantioselective palladium-catalyzed total synthesis of vitamin e by employing a domino Wacker-Heck reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 8770-6. PMID 17001611 DOI: 10.1002/chem.200600849  0.6
2006 Tietze LF, Major F, Schuberth I. Antitumor agents: development of highly potent glycosidic duocarmycin analogues for selective cancer therapy. Angewandte Chemie (International Ed. in English). 45: 6574-7. PMID 16960905 DOI: 10.1002/anie.200600936  0.6
2006 Tietze LF, Krewer B, Frauendorf H, Major F, Schuberth I. Investigation of reactivity and selectivity of DNA-alkylating duocarmycin analogues by high-resolution mass spectrometry. Angewandte Chemie (International Ed. in English). 45: 6570-4. PMID 16960904 DOI: 10.1002/anie.200600935  0.6
2006 Tietze LF, Kinzel T, Schmatz S. Origin of syn/anti diastereoselectivity in aldehyde and ketone crotylation reactions: a combined theoretical and experimental study. Journal of the American Chemical Society. 128: 11483-95. PMID 16939272 DOI: 10.1021/ja062528v  0.6
2006 Tietze LF, Brasche G, Stadler C, Grube A, Böhnke N. Multiple palladium-catalyzed reactions for the synthesis of analogues of the highly potent insecticide spinosyn A. Angewandte Chemie (International Ed. in English). 45: 5015-8. PMID 16819747 DOI: 10.1002/anie.200601003  0.6
2006 Tietze LF, Gericke KM, Güntner C. First total synthesis of the bioactive anthraquinone kwanzoquinone C and related natural products by a Diels-Alder approach European Journal of Organic Chemistry. 4910-4915. DOI: 10.1002/ejoc.200600634  0.6
2006 Tietze LF, Lotz F. Pd-catalysed domino arylation/CH activation for the synthesis of acenaphthylenes European Journal of Organic Chemistry. 4676-4684. DOI: 10.1002/ejoc.200600428  0.6
2006 Tietze LF, Major F. Synthesis of new water-soluble DNA-binding subunits for analogues of the cytotoxic antibiotic CC-1065 and their prodrugs European Journal of Organic Chemistry. 2314-2321. DOI: 10.1002/ejoc.200500060  0.6
2006 Tietze LF, Wilckens KF, Yilmaz S, Stecker F, Zinngrebe J. Synthesis of 2,3-dihydrobenzo[1,4]dioxins and -oxazins via a domino wacker-heck reaction Heterocycles. 70: 309-319.  0.6
2005 Yang SB, Major F, Tietze LF, Rupnik M. Block of delayed-rectifier potassium channels by reduced haloperidol and related compounds in mouse cortical neurons. The Journal of Pharmacology and Experimental Therapeutics. 315: 352-62. PMID 16014573 DOI: 10.1124/jpet.105.086561  0.6
2005 El Bialy SAA, Braun H, Tietze LF. Enantioselective synthesis of α-alkylmalates as the pharmacophoric group of several natural alkaloids and glycosides European Journal of Organic Chemistry. 2965-2972. DOI: 10.1002/ejoc.200500065  0.6
2005 Tietze LF, Güntner C, Gericke KM, Schuberth I, Bunkoczi G. A Diels-Alder reaction for the total synthesis of the novel antibiotic antitumor agent mensacarcin European Journal of Organic Chemistry. 2459-2467. DOI: 10.1002/ejoc.200400826  0.6
2005 Tietze LF, Stewart SG, Polomska ME. 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 European Journal of Organic Chemistry. 1752-1759. DOI: 10.1002/ejoc.200400786  0.6
2005 Tietze LF, Haunert F. Domino Reaction in Organic Synthesis. An Approach to Efficiency, Elegance, Ecological Benefit, Economic Advantage and Preservation of Our Resources in Chemical Transformations Stimulating Concepts in Chemistry. 39-64. DOI: 10.1002/3527605746.ch4  0.6
2005 Tietze LF, Rackelmann N. The Domino-Knoevenagel-Hetero-Diels-Alder Reaction and Related Transformations Multicomponent Reactions. 121-168. DOI: 10.1002/3527605118.ch5  0.6
2005 Elghamry I, Tietze LF. Linearly -π- extended porphyrins: Synthesis of novel tetrabenzoylporphyrins Journal of Heterocyclic Chemistry. 42: 503-508.  0.6
2004 Tietze LF, Sommer KM, Zinngrebe J, Stecker F. Palladium-catalyzed enantioselective domino reaction for the efficient synthesis of vitamin E. Angewandte Chemie (International Ed. in English). 44: 257-9. PMID 15565667 DOI: 10.1002/anie.200461629  0.6
2004 El Bialy SA, Braun H, Tietze LF. A highly efficient synthesis of the erythrina and B-homoerythrina skeleton by an AlMe3-mediated domino reaction. Angewandte Chemie (International Ed. in English). 43: 5391-3. PMID 15468076 DOI: 10.1002/anie.200460283  0.6
2004 Tietze LF, Stewart SG, Polomska ME, Modi A, Zeeck A. Towards a total synthesis of the new anticancer agent mensacarcin: synthesis of the carbocyclic core. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 5233-42. PMID 15372645 DOI: 10.1002/chem.200400342  0.6
2004 Tietze LF, Ila H, Bell HP. Enantioselective palladium-catalyzed transformations. Chemical Reviews. 104: 3453-516. PMID 15250747 DOI: 10.1021/cr030700x  0.6
2004 Tietze LF, Rackelmann N, Müller I. Enantioselective total syntheses of the Ipecacuanha alkaloid emetine, the Alangium alkaloid tubulosine and a novel benzoquinolizidine alkaloid by using a domino process. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 2722-31. PMID 15195303 DOI: 10.1002/chem.200306039  0.6
2004 Tietze LF, Lücke LP, Major F, Müller P. Efficient synthesis of an enantiopure thiasteroid by a double heck reaction Australian Journal of Chemistry. 57: 635-640. DOI: 10.1071/CH04034  0.6
2004 El Bialy SAA, Braun H, Tietze LF. Synthesis of azaspiro[4.4]nonanes as key structures of several bioactive natural products Synthesis. 2249-2262. DOI: 10.1055/s-2004-831198  0.6
2004 Tietze LF, Hölsken S, Adrio J, Kinzel T, Wegner C. Facial-selective allylation of methyl ketones for the asymmetric synthesis of tertiary homoallylic ethers Synthesis. 2236-2239. DOI: 10.1055/s-2004-829153  0.6
2004 Tietze LF, Matthias Wiegand J, Vock CA. Synthesis of a novel enantiopure spiro-b-norestradiol analogue by multiple Pd-catalyzed transformations European Journal of Organic Chemistry. 4107-4112. DOI: 10.1002/ejoc.200400263  0.6
2004 Tietze LF, Rackelmann N. Domino reactions in the synthesis of heterocyclic natural products and analogs Pure and Applied Chemistry. 76: 1967-1983.  0.6
2004 Tietze LF, Lohmann JK, Stadler C. Synthesis of novel highly active thiophene and benzothiophene containing diphosphine ligands and their use in the asymmetric allylation of catechol Synlett. 1113-1116.  0.6
2004 Tietze LF, Rackelmann N. Enantioselective synthesis of Epi-emetine analogues: Control of the facial selectivity in a three-component domino Knoevenagel-hetero-Diels-Alder reaction Zeitschrift Fur Naturforschung - Section B Journal of Chemical Sciences. 59: 468-477.  0.6
2004 Wölfling J, Frank E, Schneider G, Tietze LF. Synthesis of Novel D-Secoestrone Isoquinuclidines by an Unpredicted Iminium Ion-Induced 1,5-Hydride Shift European Journal of Organic Chemistry. 90-100.  0.6
2003 Tietze LF, Feuerstein T. Enzyme and proton-activated prodrugs for a selective cancer therapy Current Pharmaceutical Design. 9: 2155-2175. PMID 14529411 DOI: 10.2174/1381612033454072  0.6
2003 Tietze LF, Rackelmann N, Sekar G. Catalyst-controlled stereoselective combinatorial synthesis. Angewandte Chemie (International Ed. in English). 42: 4254-7. PMID 14502750 DOI: 10.1002/anie.200351129  0.6
2003 Tietze LF, Bell HP, Chandrasekhar S. Natural product hybrids as new leads for drug discovery. Angewandte Chemie (International Ed. in English). 42: 3996-4028. PMID 12973759 DOI: 10.1002/anie.200200553  0.6
2003 Tietze LF, Griesbach U, Schuberth I, Bothe U, Marra A, Dondoni A. Novel carboranyl C-glycosides for the treatment of cancer by boron neutron capture therapy. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 1296-302. PMID 12645018 DOI: 10.1002/chem.200390148  0.6
2003 Tietze LF, Feuerstein T. Highly selective compounds for the antibody-directed enzyme prodrug therapy of cancer Australian Journal of Chemistry. 56: 841-854. DOI: 10.1071/CH03036  0.6
2003 Tietze LF, Wiegand JM, Vock C. Synthesis of enantiopure B-nor-steroids by multiple Pd-catalyzed transformations Journal of Organometallic Chemistry. 687: 346-352. DOI: 10.1016/S0022-328X(03)00720-4  0.6
2003 Tietze LF, Sommer KM, Schneider G, Tapolcsányi P, Wölfling J, Müller P, Noltemeyer M, Terlau H. Novel medium ring sized estradiol derivatives by intramolecular Heck reactions Synlett. 1494-1496.  0.6
2003 Tietze LF, Looft J, Feuerstein T. Synthesis of ring size seco-analogs of the antitumor antibiotic CC-1065 by two consecutive transition metal-initiated transformations European Journal of Organic Chemistry. 2749-2755.  0.6
2003 Tietze LF, Haunert F, Feuerstein T, Herzig T. A concise and efficient synthesis of seco-duocarmycin SA European Journal of Organic Chemistry. 562-566.  0.6
2003 Tietze LF, Ramachandar T, Vock C. Stereoselective synthesis of new enantiopure building blocks for the preparation of steroids Synlett. 118-120.  0.6
2002 Alves F, Borchers U, Keim H, Fortte R, Olschimke J, Vogel WF, Halfter H, Tietze LF. Inhibition of EGF-mediated receptor activity and cell proliferation by HK1-ceramide, a stable analog of the ganglioside GM3-lactone. Glycobiology. 12: 517-22. PMID 12145192  0.6
2002 Tietze LF, Krahnert WR. Stereoselective synthesis of structurally simplified cephalostatin analogues by multiple Heck reactions and their biological evaluation. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 2116-25. PMID 11981896 DOI: 10.1002/1521-3765(20020503)8:9<2116::AID-CHEM2116>3.0.CO;2-4  0.6
2002 Tietze LF, Griesbach U, Bothe U, Nakamura H, Yamamoto Y. Novel carboranes with a DNA binding unit for the treatment of cancer by boron neutron capture therapy. Chembiochem : a European Journal of Chemical Biology. 3: 219-25. PMID 11921401 DOI: 10.1002/1439-7633(20020301)3:2/3<219::AID-CBIC219>3.0.CO;2-#  0.6
2002 Tietze LF, Kahle K, Raschke T. Efficient synthesis of tetrasubstituted alkenes by allylsilane-terminated domino-Heck double cyclisation. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 401-7. PMID 11843153 DOI: 10.1002/1521-3765(20020118)8:2<401::AID-CHEM401>3.0.CO;2-C  0.6
2002 Tietze LF, Feuerstein T, Fecher A, Haunert F, Panknin O, Borchers U, Schuberth I, Alves F. Proof of principle in the selective treatment of cancer by antibody-directed enzyme prodrug therapy: The development of a highly potent prodrug Angewandte Chemie - International Edition. 41: 759-761. DOI: 10.1002/1521-3773(20020301)41:5<759::AID-ANIE759>3.0.CO;2-7  0.6
2002 Tietze LF, Lohmann JK. Synthesis of novel chiral thiophene-, benzothiophene- and benzofuran-oxazoline ligands and their use in the enantioselective Pd-catalyzed allylation Synlett. 2083-2085.  0.6
2002 Tietze LF, Griesbach U, Elsner O. Efficient synthesis of ortho-carborane by reaction of propiolic acid tert-butyl ester with decaborane(14) Synlett. 1109-1110.  0.6
2002 Tietze LF, Herzig T, Feuerstein T, Schuberth I. Synthesis and biological evaluation of novel analogues and prodrugs of the cytotoxic antibiotic CC-1065 for selective cancer therapy European Journal of Organic Chemistry. 1634-1645.  0.6
2001 Tietze LF, Herzig T, Fecher A, Haunert F, Schuberth I. Highly selective glycosylated prodrugs of cytostatic CC-1065 analogues for antibody-directed enzyme tumor therapy. Chembiochem : a European Journal of Chemical Biology. 2: 758-65. PMID 11948858 DOI: 10.1002/1439-7633(20011001)2:10<758::AID-CBIC758>3.0.CO;2-G  0.6
2001 Tietze LF, Bothe U, Griesbach U, Nakaichi M, Hasegawa T, Nakamura H, Yamamoto Y. Carboranyl bisglycosides for the treatment of cancer by boron neutron capture therapy. Chembiochem : a European Journal of Chemical Biology. 2: 326-34. PMID 11828461 DOI: 10.1002/1439-7633(20010504)2:5<326::AID-CBIC326>3.0.CO;2-Y  0.6
2001 Tietze LF, Lieb M, Herzig T, Haunert F, Schuberth I. A strategy for tumor-selective chemotherapy by enzymatic liberation of seco-duocarmycin SA-derivatives from nontoxic prodrugs. Bioorganic & Medicinal Chemistry. 9: 1929-39. PMID 11425596 DOI: 10.1016/S0968-0896(01)00098-0  0.6
2001 Tietze LF, Bothe U, Griesbach U, Nakaichi M, Hasegawa T, Nakamura H, Yamamoto Y. Ortho-carboranyl glycosides for the treatment of cancer by boron neutron capture therapy. Bioorganic & Medicinal Chemistry. 9: 1747-52. PMID 11425576 DOI: 10.1016/S0968-0896(01)00061-X  0.6
2001 Tietze LF, Völkel L, Wulff C, Weigand B, Bittner C, McGrath P, Johnson K, Schäfer M. Facial-selective allylation of methyl ketones for the asymmetric synthesis of alpha-substituted tertiary homoallylic ethers. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 1304-8. PMID 11322558 DOI: 10.1002/1521-3765(20010316)7:6<1304::AID-CHEM1304>3.0.CO;2-9  0.6
2001 Alves F, Borchers U, Padge B, Augustin H, Nebendahl K, Klöppel G, Tietze LF. Inhibitory effect of a matrix metalloproteinase inhibitor on growth and spread of human pancreatic ductal adenocarcinoma evaluated in an orthotopic severe combined immunodeficient (SCID) mouse model. Cancer Letters. 165: 161-70. PMID 11275365 DOI: 10.1016/S0304-3835(01)00420-7  0.6
2001 Tietze LF, Kettschau G, Heuschert U, Nordmann G. Highly efficient synthesis of linear pyrrole oligomers by twofold Heck reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 368-73. PMID 11271522 DOI: 10.1002/1521-3765(20010119)7:2<368::AID-CHEM368>3.0.CO;2-2  0.6
2001 Tietze LF, Evers H, Töpken E. A Novel Concept in Combinatorial Chemistry in Solution with the Advantages of Solid-Phase Synthesis: Formation of N-Betaines by Multicomponent Domino Reactions This work was supported as part of the BMBF Project "Kombinatorische Chemie" (grant number 03 D0056 2). We thank BASF AG, Ludwigshafen, and the Fonds der Chemischen Industrie for generous support. Angewandte Chemie (International Ed. in English). 40: 903-905. PMID 11241641 DOI: 10.1002/1521-3773(20010302)40:5<903::AID-ANIE903>3.0.CO;2-7  0.6
2001 Tietze LF, Völkel L. Total Synthesis of the Macrolide Antibiotic 5,6-Dihydrocineromycin B This work was supported by the DFG (SFB 416) and the Fonds der Chemischen Industrie. We thank Prof. Dr. A. Zeeck for supplying data of the title compound, as well as BASF, Degussa-Hüls and Wacker-Chemie for donations of chemicals. Angewandte Chemie (International Ed. in English). 40: 901-902. PMID 11241640 DOI: 10.1002/1521-3773(20010302)40:5<901::AID-ANIE901>3.0.CO;2-F  0.6
2001 Tietze LF, Weigand B, Völkel L, Wulff C, Bittner C. Synthesis of enantiopure homoallylic ethers by reagent controlled facial selective allylation of chiral ketones. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 161-8. PMID 11205007 DOI: 10.1002/1521-3765(20010105)7:1<161::AID-CHEM161>3.0.CO;2-9  0.6
2001 Tietze LF, Ott C, Haunert F. Efficient and regioselective synthesis of bridged ring systems by domino Knoevenagel - hetero-Diels-Alder reaction Canadian Journal of Chemistry. 79: 1511-1514. DOI: 10.1139/cjc-79-11-1511  0.6
2001 Attanasi OA, De Crescentini L, Filippone P, Mantellini F, Tietze LF. 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. 57: 5855-5863. DOI: 10.1016/S0040-4020(01)00523-3  0.6
2001 Tietze LF, Steck PL. A domino spirocyclization to form lactams European Journal of Organic Chemistry. 4353-4356.  0.6
2001 Tietze LF, Nordmann G. A novel palladium-catalyzed domino Tsuji-Trost-Heck process for the synthesis of tetrahydroanthracenes European Journal of Organic Chemistry. 3247-3253.  0.6
2001 Tietze LF, Ott C, Geißler H, Haunert F. Regioselective reduction and ring cleavage of polycyclic barbituric acid analogues derived from intramolecular hetero-Diels-Alder reactions European Journal of Organic Chemistry. 1625-1630.  0.6
2001 Tietze LF, Petersen S. Stereoselective synthesis of novel 19-nor-steroids by a double Heck reaction European Journal of Organic Chemistry. 1619-1624.  0.6
2001 Tietze LF, Evers H, Hippe T, Steinmetz A, Töpken E. Solid-phase synthesis of substituted pyrazolones from polymer-bound β-keto esters European Journal of Organic Chemistry. 1631-1634.  0.6
2001 Tietze LF, Nordmann G. Synthesis of a linear oligomeric styrylpyrrole using multiple heck and wittig reactions Synlett. 337-340.  0.6
2001 Tietze LF, Krahnert WR. Selective synthesis of bissteroidal compounds by multifold Heck reactions Synlett. 560-562.  0.6
2000 Tietze LF, Schneider G, Wölfling J, Fecher A, Nöbel T, Petersen S, Schuberth I, Wulff C. A novel approach in drug discovery: synthesis of estrone--talaromycin natural product hybrids. Chemistry (Weinheim An Der Bergstrasse, Germany). 6: 3755-60. PMID 11073246 DOI: 10.1002/1521-3765(20001016)6:20<3755::AID-CHEM3755>3.0.CO;2-L  0.6
2000 Kirschning A, Chen GW, Dräger G, Schuberth I, Tietze LF. Syntheses and biological evaluation of new glyco-modified angucyclin-antibiotics. Bioorganic & Medicinal Chemistry. 8: 2347-54. PMID 11026547 DOI: 10.1016/S0968-0896(00)00166-8  0.6
2000 Tietze LF, Keim H, Janssen CO, Tappertzhofen C, Olschimke J. Synthesis of a novel ether-bridged GM3-lactone analogue as a target for an antibody-based cancer therapy. Chemistry (Weinheim An Der Bergstrasse, Germany). 6: 2801-8. PMID 10985728 DOI: 10.1002/1521-3765(20000804)6:15<2801::AID-CHEM2801>3.0.CO;2-X  0.6
2000 Tietze LF, Modi A. Multicomponent domino reactions for the synthesis of biologically active natural products and drugs. Medicinal Research Reviews. 20: 304-22. PMID 10861729 DOI: 10.1002/1098-1128(200007)20:4<304::AID-MED3>3.0.CO;2-8  0.6
2000 Tietze LF, Bothe U, Schuberth I. 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. Chemistry (Weinheim An Der Bergstrasse, Germany). 6: 836-42. PMID 10826605 DOI: 10.1002/(SICI)1521-3765(20000303)6:5<836::AID-CHEM836>3.0.CO;2-8  0.6
2000 Tietze LF, Schirok H, Wöhrmann M. Palladium-catalyzed synthesis of cephalotaxine analogues. Chemistry (Weinheim An Der Bergstrasse, Germany). 6: 510-8. PMID 10747418 DOI: 10.1002/(SICI)1521-3765(20000204)6:3<510::AID-CHEM510>3.0.CO;2-H  0.6
2000 Tietze LF, Thede K. Highly regio- and enantioselective heck reactions of N-substituted 2-pyrroline with the new chiral ligand BITIANP Synlett. 1470-1472.  0.6
2000 Tietze LF, Schirok H, Wöhrmann M, Schrader K. Efficient synthesis of six-membered ring D analogues of the pentacyclic alkaloid cephalotaxine by two palladium-catalyzed reactions European Journal of Organic Chemistry. 2433-2444.  0.6
2000 Tietze LF, Zhou Y, Töpken E. Synthesis of simple enantiopure tetrahydro-β-carbolines and tetrahydroisoquinolines European Journal of Organic Chemistry. 2247-2252.  0.6
2000 Tietze LF, Modi A. Regioselective silane-terminated intramolecular heck reaction with alkenyl triflates and alkenyl iodides European Journal of Organic Chemistry. 1959-1964.  0.6
2000 Tietze LF, Petersen S. Stereoselective total synthesis of a novel D-homosteroid by a twofold heck reaction European Journal of Organic Chemistry. 1827-1830.  0.6
2000 Tietze LF, Thede K, Schimpf R, Sannicolò F. Enantioselective synthesis of tetrahydroisoquinolines and benzazepines by silane terminated heck reactions with the chiral ligands (+)-TMBTP and (R)-BITIANP Chemical Communications. 583-584.  0.6
2000 Tietze LF, Weigand B, Wulff C. A mild and efficient method for the preparation of 1,3-dithianes from aldehydes and ketones Synthesis. 69-71.  0.6
1999 Tietze LF, Schirok H. Enantioselective highly efficient synthesis of (-)-cephalotaxine using two palladium-catalyzed transformations Journal of the American Chemical Society. 121: 10264-10269. DOI: 10.1021/ja991650+  0.6
1999 Attanasi OA, Filippone P, Guidi B, Hippe T, Mantellini F, Tietze LF. First preparation and reaction of polymer-bound 1,2-diaza-1,3-butadienes. A convenient entry to 4-triphenylphosphoranylidene-4,5-dihydropyrazol-5-ones Tetrahedron Letters. 40: 9277-9280. DOI: 10.1016/S0040-4039(99)01893-6  0.6
1999 Tietze LF, Henrich M, Niklaus A, Buback M. The effect of high pressure on the diastereoselectivity of intermolecular all-carbon Diels-Alder reactions Chemistry - a European Journal. 5: 297-304. DOI: 10.1002/(SICI)1521-3765(19990104)5:1<297::AID-CHEM297>3.0.CO;2-5  0.6
1999 Wölfling J, Frank E, Schneider G, Tietze LF. Synthesis of novel steroid alkaloids by cyclization of arylimines from estrone European Journal of Organic Chemistry. 3013-3020.  0.6
1999 Tietze LF, Wegner C, Wulff C. First total synthesis and determination of the absolute configuration of the stress factor (+)-hydroxymyoporone Chemistry - a European Journal. 5: 2885-2889.  0.6
1999 Tietze LF, Thede K, Sannicolò F. Regio- and enantio-selective Heck reactions of aryl and alkenyl triflates with the new chiral ligand (R)-BITIANP Chemical Communications. 1811-1812.  0.6
1999 Tietze LF, Zhou Y. Highly efficient, enantioselective total synthesis of the active anti- influenza A virus indole alkaloid hirsutine and related compounds by domino reactions Angewandte Chemie - International Edition. 38: 2045-2047.  0.6
1999 Tietze LF, Görlitzer J, Schuffenhauer A, Hübner M. Enantioselective synthesis of the chromane moiety of vitamin E European Journal of Organic Chemistry. 1075-1084.  0.6
1999 Wölfling J, Frank E, Schneider G, Tietze LF. Synthesis of unusual bridged steroid alkaloids by an iminium ion induced 1,5-shift of a benzylic hydride Angewandte Chemie - International Edition. 38: 200-201.  0.6
1999 Tietze LF, Nordmann G. Synthesis of 5,5''-bisfunctionalized 2,2': 6',2''-terpyridines using functionalized pyridine building blocks Synlett. 342-344.  0.6
1998 Tietze LF, Lieb ME. Domino reactions for library synthesis of small molecules in combinatorial chemistry. Current Opinion in Chemical Biology. 2: 363-71. PMID 9691073  0.6
1998 Tietze LF, Pfeiffer T, Schuffenhauer A. Stereoselective Intramolecular Hetero Diels-Alder Reactions of Cyclic Benzylidenesulfoxides and DFT Calculations on the Transition Structures European Journal of Organic Chemistry. 2733-2741.  0.6
1998 Wölfling J, Frank E, Schneider G, Bes MT, Tietze LF. Synthesis of azasteroids and D-homosteroids by intramolecular cyclization reactions of steroid arylimines Synlett. 1205-1206.  0.6
1996 Tietze LF. Domino Reactions in Organic Synthesis. Chemical Reviews. 96: 115-136. PMID 11848746 DOI: 10.1002/9783527609925  0.6
1989 Tietze LF, Fischer R, Lögers M, Beller M. Stereoselective synthesis of 1,1-dialkyl-1-methoxymethyl glucosides (acetal-glucosides). Carbohydrate Research. 194: 155-62. PMID 2620298  0.4
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