Tietze, Lutz F., Hannemann, Robert, Buhr, Wilm, Lögers, Michael, Menningen, Pia, Lieb, Monika, Starck, Dorothea, Grote, Thomas, Döring, Angela, Schuberth, Ingrid (1996) Tumorselektiv aktivierbare Prodrugs des Cytostaticums CC-1065. Angewandte Chemie, 108 (22). 2840-2842 doi:10.1002/ange.19961082229

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Reference Type	Journal (article/letter/editorial)
Title	Tumorselektiv aktivierbare Prodrugs des Cytostaticums CC-1065
Journal	Angewandte Chemie
Authors	Tietze, Lutz F.		Author
	Hannemann, Robert		Author
	Buhr, Wilm		Author
	Lögers, Michael		Author
	Menningen, Pia		Author
	Lieb, Monika		Author
	Starck, Dorothea		Author
	Grote, Thomas		Author
	Döring, Angela		Author
	Schuberth, Ingrid		Author
Year	1996 (November 18)	Volume	108
Issue	22
Publisher	Wiley
DOI	doi:10.1002/ange.19961082229Search in ResearchGate
	Generate Citation Formats
Mindat Ref. ID	7293042	Long-form Identifier	mindat:1:5:7293042:9
GUID	0
Full Reference	Tietze, Lutz F., Hannemann, Robert, Buhr, Wilm, Lögers, Michael, Menningen, Pia, Lieb, Monika, Starck, Dorothea, Grote, Thomas, Döring, Angela, Schuberth, Ingrid (1996) Tumorselektiv aktivierbare Prodrugs des Cytostaticums CC-1065. Angewandte Chemie, 108 (22). 2840-2842 doi:10.1002/ange.19961082229
Plain Text	Tietze, Lutz F., Hannemann, Robert, Buhr, Wilm, Lögers, Michael, Menningen, Pia, Lieb, Monika, Starck, Dorothea, Grote, Thomas, Döring, Angela, Schuberth, Ingrid (1996) Tumorselektiv aktivierbare Prodrugs des Cytostaticums CC-1065. Angewandte Chemie, 108 (22). 2840-2842 doi:10.1002/ange.19961082229
In	(1996, November) Angewandte Chemie Vol. 108 (22) Wiley

	Tietze, Lutz F., Buhr, Wilm (1995) Effiziente Totalsynthese der pharmakophoren Gruppe des Antitumorantibioticums CC-1065 durch kombinierte mit einem Zirconocen- und Palladium-Komplex initiierte Cyclisierungen. Angewandte Chemie, 107 (12). 1485-1487 doi:10.1002/ange.19951071228
	Tietze, Lutz F., Buhr, Wilm, Looft, Jan, Grote, Thomas (1998) Efficient Synthesis of the Pharmacophore of the Highly Potent Antitumor Antibiotic CC-1065. Chemistry - A European Journal, 4 (8). 1554-1560 doi:10.1002/(sici)1521-3765(19980807)4:8<1554::aid-chem1554>3.0.co;2-j
	Tietze, Lutz F., von Hof, J. Marian, Müller, Michael, Krewer, Birgit, Schuberth, Ingrid (2010) Glycosidische Prodrugs hochpotenter difunktioneller Duocarmycin-Derivate für eine selektive Tumortherapie. Angewandte Chemie, 122 (40). 7494-7497 doi:10.1002/ange.201002502
	Tietze, Lutz F., von Hof, J. Marian, Müller, Michael, Krewer, Birgit, Schuberth, Ingrid (2010) Glycosidic Prodrugs of Highly Potent Bifunctional Duocarmycin Derivatives for Selective Treatment of Cancer. Angewandte Chemie International Edition, 49 (40). 7336-7339 doi:10.1002/anie.201002502
	Tietze, Lutz F., Major, Felix, Schuberth, Ingrid (2006) Antitumor-Wirkstoffe: Entwicklung hochpotenter glycosidischer Duocarmycin-Analoga für eine selektive Krebstherapie. Angewandte Chemie, 118 (39). 6724-6727 doi:10.1002/ange.200600936
	*Tietze, Lutz F., Nöbel, Thomas, Spescha, Maurus (1996) Stereoselektive Synthese von Steroiden durch Heck-Reaktion. Angewandte Chemie, 108 (19). 2385-2386 doi:10.1002/ange.19961081922*
	Tietze, Lutz F., Grote, Thomas (1993) Anticancer Agents, 19[1]. Synthesis of the Reduced A-Unit (CI) of the Antitumor Antibiotic CC-1065. Chemische Berichte, 126. 2733-2737 doi:10.1002/cber.19931261224
	Tietze, Lutz F., Krewer, Birgit, Frauendorf, Holm, Major, Felix, Schuberth, Ingrid (2006) Untersuchung der Reaktivität und Selektivität DNA-alkylierender Duocarmycin-Analoga mittels hochauflösender Massenspektrometrie. Angewandte Chemie, 118 (39). 6720-6724 doi:10.1002/ange.200600935
	Tietze, Lutz F., Beller, Matthias, Fischer, Roland, Lögers, Michael, Jähde, Eckhard, Glüsenkamp, Karl-Heinz, Rajewsky, Manfred F. (1990) Entwicklung maßgeschneiderter, säurekatalytisch aktivierbarer Cytostatika für eine selektive Tumortherapie. Angewandte Chemie, 102 (7). 812-813 doi:10.1002/ange.19901020717
	Tietze, Lutz F., Müller, Michael, Duefert, Svenia-C., Schmuck, Kianga, Schuberth, Ingrid (2013) Photoactivatable Prodrugs of Highly Potent Duocarmycin Analogues for a Selective Cancer Therapy. Chemistry - A European Journal, 19 (5). 1726-1731 doi:10.1002/chem.201202773
	Tietze, Lutz F., Schmuck, Kianga, Schuster, Heiko J., Müller, Michael, Schuberth, Ingrid (2011) Synthesis and Biological Evaluation of Prodrugs Based on the Natural Antibiotic Duocarmycin for Use in ADEPT and PMT. Chemistry - A European Journal, 17 (6). 1922-1929 doi:10.1002/chem.201002798

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