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G. Valdomir, L.F. Tietze Chromanone Lactones: A Neglected Group of Natural Products - Isolation, Structure Elucidation, Bioactivity, and Synthesis. Eur.J.Org.Chem. 2022, 20, 28-55. Online
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
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
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
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
L.F. Tietze, T. Kinzel Synthesis of natural products and analogs using multiple Pd-catalyzed transformations. Pure Appl. Chem. 2007, 79, 629-650. Online
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.
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.
L.F. Tietze, N.Rackelmann Domino reactions in the synthesis of heterocyclic natural products and analogs. Pure Appl. Chem. 2004, 76, 1967-1983.
S. A. A. El Bialy, H. Braun and L.F. Tietze Synthesis of Azaspiro[4.4]nonanes as Key Structures of Several Bioactive Natural Products. Synthesis 2004, 14, 2249-2262.
L.F. Tietze, H. Ila and H. P. Bell Enantioselective Palladium-Catalyzed Transformations. Chem. Rev. 2004, 104, 3453-3516.
L.F. Tietze, S. Chandrasekhar and 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.
L.F. Tietze and T. Feuerstein Highly Selective Compounds for the Antibody-Directed Enzyme Prodrug Therapy of Cancer. Aust. J. Chem., 2003, 56, 841-854.
L.F. Tietze and A. Modi Multi-component Domino Reactions for the Synthesis of Biological Active Natural Products and Drugs. Medicinal Research Reviews 2000, 20, 4, 304-322.
L.F. Tietze and M. Lieb Domino Reactions for Library Synthesis of Small Molecules in Combinatorial Chemistry. Current Opinion in Chemical Biology 1998, 2, 363-371.
L.F. Tietze, G. Kettschau, J. A. Gewert and A. Schuffenhauer Hetero-Diels-Alder Reactions of 1-Oxa-1,3-butadienes. Current Organic Chemistry 1998, 2, 19-62.
L.F. Tietze Dominoreaktionen. Nachr. Chem. Tech. Lab. 1997, 45, 1181-1187.
L.F. Tietze and G. Kettschau  Hetero-Diels-Alder Reactions. Topics in Current Chemistry 1997, 189, 1-120.
L.F. Tietze Domino Reactions in Organic Synthesis. Chem. Rev. 1996, 96, 115-136.
L.F. Tietze  Domino Reactions in Organic Synthesis. Chemistry and Industry 1995, 453-457.
L.F. Tietze and U. Beifuss Sequential transformations in organic chemistry: a synthesis strategy with a future. Angew. Chem., 1993, 105, 137-170; Angew. Chem. Int. Ed. Engl. 1993, 32, 131-163.
L.F. Tietze Domino-reactions: The tandem-Knoevenagel-hetero-Diels-Alder reaction and its application in natural product synthesis. Journal of Heterocyclic Chem., 1990, 27, 47-69.
L.F. Tietze Concepts for a selective chemotherapy of malignant tumors. Nachrichten aus Chemie, Technik und Laboratorium, 1988, 36, 728-737.
L.F. Tietze Secologanin, a biogenetic key compound - synthesis and biogenesis of iridoidal and secoiridoidal glycosides. Angew. Chem., 1983, 95, 840-853; Angew. Chem. Int. Ed. Engl. 1983, 22, 828.

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Last Update 09. April 2018 Please report any error to Martina Pretor