Authors:
Tietze, LF
Bothe, U
Griesbach, U
Nakaichi, M
Hasegawa, T
Nakamura, H
Yamamoto, Y
Citation: Lf. Tietze et al., Carboranyl bisglycosides for the treatment of cancer by boron neutron capture therapy, CHEMBIOCHEM, 2(5), 2001, pp. 326-334
Citation: Lf. Tietze et S. Petersen, Stereoselective synthesis of novel 19-nor-steroids by a double Heck reaction, EUR J ORG C, (9), 2001, pp. 1619-1624
Citation: Lf. Tietze et al., Regioselective reduction and ring cleavage of polycyclic barbituric acid analogues derived from intramolecular hetero-Diels-Alder reactions, EUR J ORG C, (9), 2001, pp. 1625-1630
Citation: Lf. Tietze et G. Nordmann, A novel palladium-catalyzed domino Tsuji-Trost-Heck process for the synthesis of tetrahydroanthracenes, EUR J ORG C, (17), 2001, pp. 3247-3253
Citation: Lf. Tietze et al., A novel concept in combinatorial chemistry in solution with the advantagesof solid-phase synthesis: Formation of N-betaines by multicomponent dominoreactions, ANGEW CHEM, 40(5), 2001, pp. 903-905
Authors:
Tietze, LF
Bothe, U
Griesbach, U
Nakaichi, M
Hasegawa, T
Nakamura, H
Yamamoto, Y
Citation: Lf. Tietze et al., ortho-Carboranyl glycosides for the treatment of cancer by boron neutron capture therapy, BIO MED CH, 9(7), 2001, pp. 1747-1752
Authors:
Tietze, LF
Lieb, M
Herzig, T
Haunert, F
Schuberth, I
Citation: Lf. Tietze et al., A strategy for tumor-selective chemotherapy by enzymatic liberation of seco-duocarmycin SA-derivatives from nontoxic prodrugs, BIO MED CH, 9(7), 2001, pp. 1929-1939
Authors:
Tietze, LF
Volkel, L
Wulff, C
Weigand, B
Bittner, C
McGrath, P
Johnson, K
Schafer, M
Citation: Lf. Tietze et al., Facial-selective allylation of methyl ketones for the asymmetric synthesisof alpha-substituted tertiary homoallylic ethers, CHEM-EUR J, 7(6), 2001, pp. 1304-1308
Authors:
Tietze, LF
Weigand, B
Volkel, L
Wulff, C
Bittner, C
Citation: Lf. Tietze et al., Synthesis of enantiopure homoallylic ethers by reagent controlled facial selective allylation of chiral ketones, CHEM-EUR J, 7(1), 2001, pp. 161-168
Citation: Lf. Tietze et G. Nordmann, Synthesis of a linear oligomeric styrylpyrrole using multiple Heck and Wittig reactions, SYNLETT, (3), 2001, pp. 337-340
Authors:
Alves, F
Borchers, U
Padge, B
Augustin, H
Nebendahl, K
Kloppel, G
Tietze, LF
Citation: F. Alves et al., 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 LETT, 165(2), 2001, pp. 161-170
Authors:
Attanasi, OA
De Crescentini, L
Filippone, P
Mantellini, F
Tietze, LF
Citation: Oa. Attanasi et al., 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(27), 2001, pp. 5855-5863
Citation: Lf. Tietze et S. Petersen, Stereoselective total synthesis of a novel D-homosteroid by a twofold Heckreaction, EUR J ORG C, (9), 2000, pp. 1827-1830
Authors:
Tietze, LF
Schirok, H
Wohrmann, M
Schrader, K
Citation: Lf. Tietze et al., Efficient synthesis of six-membered ring D analogues of the pentacyclic alkaloid cephalotaxine by two palladium-catalyzed reactions, EUR J ORG C, (13), 2000, pp. 2433-2444
Citation: Lf. Tietze et al., Synthesis of simple enantiopure tetrahydro-beta-carbolines and tetrahydroisoquinolines, EUR J ORG C, (12), 2000, pp. 2247-2252
Citation: Lf. Tietze et A. Modi, Regioselective silane-terminated intramolecular Heck reaction with alkenyltriflates and alkenyl iodides, EUR J ORG C, (10), 2000, pp. 1959-1964
Authors:
Tietze, LF
Thede, K
Schimpf, R
Sannicolo, F
Citation: Lf. Tietze et al., Enantioselective synthesis of tetrahydroisoquinolines and benzazepines by silane terminated Heck reactions with the chiral ligands (+)-TMBTP and (R)-BITIANP, CHEM COMMUN, (7), 2000, pp. 583-584
Authors:
Kirschning, A
Chen, GW
Drager, G
Schuberth, I
Tietze, LF
Citation: A. Kirschning et al., Syntheses and biological evaluation of new glyco-modified angucyclin-antibiotics, BIO MED CH, 8(9), 2000, pp. 2347-2354
Citation: Lf. Tietze et al., 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 F-19-NMR spectroscopy, CHEM-EUR J, 6(5), 2000, pp. 836-842