Stanetty, C., Wolkerstorfer, A., Amer, H., Hofinger, A., Jordis, U., Claßen-Houben, D., & Kosma, P. (2012). Synthesis and antiviral activities of spacer-linked 1-thioglucuronide analogues of glycyrrhizin. Beilstein Journal of Organic Chemistry, 8, 705–711. https://doi.org/10.3762/bjoc.8.79 ( reposiTUm)

Czollner, L., Jordis, U., & Mereiter, K. (2012). (3β,18β,20β)-N-Ethoxycarbonylmethyl-3-nitrato-11-oxoolean-12-ene-29-carboxamide methanol monosolvate. Acta Crystallographica Section E: Structure Reports Online, 68(4), o1229–o1230. https://doi.org/10.1107/s1600536812012561 ( reposiTUm)

Gaware, R., Khunt, R., Czollner, L., Stanetty, C., Cunha, T. D., Kratschmar, D. V., Odermatt, A., Kosma, P., Jordis, U., & Claßen-Houben, D. (2011). Synthesis of new glycyrrhetinic acid derived ring A azepanone, 29-urea and 29-hydroxamic acid derivatives as selective 11β-hydroxysteroid dehydrogenase 2 inhibitors. Bioorganic and Medicinal Chemistry, 19(6), 1866–1880. https://doi.org/10.1016/j.bmc.2011.02.005 ( reposiTUm)

Czollner, L., Jordis, U., & Mereiter, K. (2011). Propargylaminyl 3α-hydroxy-11-oxo-18β-olean-12-en-29-oate. Acta Crystallographica Section E Structure Reports Online, 67(11), o3052–o3053. https://doi.org/10.1107/s1600536811043534 ( reposiTUm)

Stanetty, C., Czollner, L., Koller, I., Shah, P., Gaware, R., Cunha, T. D., Odermatt, A., Jordis, U., Kosma, P., & Claßen-Houben, D. (2010). Synthesis of novel 3-amino and 29-hydroxamic acid derivatives of glycyrrhetinic acid as selective 11b-hydroxysteroid dehydrogenase 2 inhibitors. Bioorganic and Medicinal Chemistry, 18(21), 7522–7541. https://doi.org/10.1016/j.bmc.2010.08.046 ( reposiTUm)

Gaware, R., Czollner, L., Jordis, U., & Mereiter, K. (2010). (+)-Methyl 3b-acetoxy-13-carboxy-19-hydroxy-11-oxo-C-norolean-18-en-30-oate c-lactone. Acta Crystallographica Section E Structure Reports Online, 66(10), o2597–o2598. https://doi.org/10.1107/s1600536810036901 ( reposiTUm)

Bartolucci, C., Haller, L. A., Jordis, U., Fels, G., & Lamba, D. (2010). Probing Torpedo californica Acetylcholinesterase Catalytic Gorge with Two Novel Bis-functional Galanthamine Derivatives. Journal of Medicinal Chemistry, 53(2), 745–751. https://doi.org/10.1021/jm901296p ( reposiTUm)

Beseda, I., Czollner, L., Shah, P., Khunt, R., Gaware, R., Kosma, P., Stanetty, C., Ruiz-Ruiz, M. C. del, Amer, H., Mereiter, K., Da Cunha, T., Odermatt, A., Claßen-Houben, D., & Jordis, U. (2010). Synthesis of glycyrrhetinic acid derivatives for the treatment of metabolic diseases. Bioorganic and Medicinal Chemistry, 18(1), 433–454. https://doi.org/10.1016/j.bmc.2009.10.036 ( reposiTUm)

Maelicke, A., Hoeffle-Maas, A., Ludwig, J., Maus, A., Samochocki, M., Jordis, U., & Koepke, A. K. E. (2010). Memogain is a Galantamine Pro-drug having Dramatically Reduced Adverse Effects and Enhanced Efficacy. Journal of Molecular Neuroscience, 40, 135–137. http://hdl.handle.net/20.500.12708/166724 ( reposiTUm)

Amer, H., Mereiter, K., Stanetty, C., Hofinger, A., Czollner, L., Beseda, I., Jordis, U., Kueenburg, B., Claßen-Houben, D., & Kosma, P. (2010). Synthesis and crystal structures of ring A modified glycyrrhetinic acid derivatives derived from 2,3-oxirane and 2,3-thiirane intermediates. Tetrahedron, 66(24), 4390–4402. https://doi.org/10.1016/j.tet.2010.03.098 ( reposiTUm)

Rabong, C., Jordis, U., & Phopase, J. B. (2010). NXO Building Blocks for Backbone Modification of Peptides and Preparation of Pseudopeptides. The Journal of Organic Chemistry, 75(8), 2492–2500. https://doi.org/10.1021/jo902518r ( reposiTUm)

Jordis, U. (2009). Reaxys. Chemistry World, 6(10), 71–72. http://hdl.handle.net/20.500.12708/167145 ( reposiTUm)

Ruiz, M. C. del R., Amer, H., Stanetty, C., Beseda, I., Czollner, L., Shah, P., Jordis, U., Kueenburg, B., Claßen-Houben, D., Hofinger, A., & Kosma, P. (2009). Efficient synthesis of glycyrrhetinic acid glycoside/glucuronide derivatives using silver zeolite as promoter. Carbohydrate Research, 344(9), 1063–1071. https://doi.org/10.1016/j.carres.2009.04.015 ( reposiTUm)

Classen-Houben, D., Schuster, D., Da Cunha, T., Odermatt, A., Wolber, G., Jordis, U., & Küenburg, B. (2009). Selective inhibition of 11beta -hydroxysteroid dehydrogenase 1 by 18alpha -glycyrrhetinic acid but not 18beta -glycyrrhetinic acid. Journal of Steroid Biochemistry and Molecular Biology, 113, 248–252. http://hdl.handle.net/20.500.12708/165443 ( reposiTUm)

Rabong, C., Hametner, C., Mereiter, K., Kartsev, V. G., & Jordis, U. (2008). Scope and limitations of the T-reaction employing some functionalized C-H-acids and naturally occurring secondary amines. Heterocycles, 75(4), 799–838. http://hdl.handle.net/20.500.12708/170305 ( reposiTUm)

Phopase, J., Jordis, U., & Ayoub, M. (2008). NXO-modified amino acids: novel building blocks for peptidomimetics. Chimica Oggi-Chemistry Today, 26(5), 53–54. http://hdl.handle.net/20.500.12708/171242 ( reposiTUm)

Jordis, U., Rabong, C., Valla, C., & Kartsev, V. G. (2007). Stereochemical outcome of the T-reaction employing chiral bicyclic amines. Mendeleev Communications, 17, 1–4. http://hdl.handle.net/20.500.12708/169386 ( reposiTUm)

Costea, L. V., Bercean, V. N., Badea, V., Gerdes, K., & Jordis, U. (2006). Synthesis and Eletrochemical Behavior of Some 1H-3-Methyl-4-ethoxycarbonyl-5-(benzylidenehydrazino)pyrazoles. Monatshefte Für Chemie - Chemical Monthly, 137, 737–744. http://hdl.handle.net/20.500.12708/173140 ( reposiTUm)

Jordis, U., & Yousefí, B. H. (2006). 4,4’-Diethylaminoethoxyhexestrol dihydrochloride. Molbank, HTTP://WWW.MDPI.ORG/MOLBANK/(M511), 1. http://hdl.handle.net/20.500.12708/173312 ( reposiTUm)

Knesl, P., Yousefí, B. H., Mereiter, K., & Jordis, U. (2006). Synthesis of (-)- and (+)-8-fluorogalanthamine. Tetrahedron Letters, 47, 5701–5703. http://hdl.handle.net/20.500.12708/173268 ( reposiTUm)

Jordis, U., Knesl, P., & Röseling, D. (2006). Improved Synthesis of Substituted 6,7-Dihydroxy-4-quinazolineamines: Tandutinib, Erlotinib and Gefitinib. Molecules, 11, 286–297. http://hdl.handle.net/20.500.12708/173293 ( reposiTUm)

Knesl, P., & Jordis, U. (2005). Synthesis of deuterated analogs of pharmaceuticals. Scientia Pharmaceutica, 73(2), 191. http://hdl.handle.net/20.500.12708/172868 ( reposiTUm)

Hametner, C., Hemetsberger, M., Treu, M., Mereiter, K., Jordis, U., & Fröhlich, J. (2005). Addition of nucleophiles to immonium galanthamines. European Journal of Organic Chemistry, 2, 404–409. http://hdl.handle.net/20.500.12708/172861 ( reposiTUm)

Gerdes, K., Kremser, J., Kappe, C., & Jordis, U. (2005). Synthesis of 2,4-dimethyl-8-[2’-(2H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-5,8-dihydro-6H-pyrido[2,3-D]pyrimidin-7-one (tasosartan) and application of microwave assisted organic synthesis. Scientia Pharmaceutica, 73(2), 189. http://hdl.handle.net/20.500.12708/172866 ( reposiTUm)

Marquardt, U., Seipelt, J., & Jordis, U. (2005). Solid phase supported synthesis of alkyl dithiocarbamates. Scientia Pharmaceutica, 73(2), 190. http://hdl.handle.net/20.500.12708/172867 ( reposiTUm)

Skubak, J., Phopase, J., & Jordis, U. (2005). Microwave Assisted and Conventional Mono Aryl Substitution of Diazabicycloalkanes by Encapsulated Palladium Coupling. Scientia Pharmaceutica, 73(2), 49. http://hdl.handle.net/20.500.12708/172865 ( reposiTUm)

Jordis, U., Grohmann, F., & Küenburg, B. (1997). Optimized synthesis of some γ,γ-disubstituted allylamines. Organic Preparations and Procedures International: The New Journal for Organic Synthesis, 29(5), 549–560. http://hdl.handle.net/20.500.12708/174664 ( reposiTUm)

Hayek, E. W. H., Krenmayr, P., Lohninger, H., Jordis, U., Sauter, F., & Moche, W. (1991). GC/MS and chemometrics in archaeometry. Investigation of glue on copper-age arrowheads. Fresenius Journal of Analytical Chemistry, 340(3), 153–156. http://hdl.handle.net/20.500.12708/174668 ( reposiTUm)

Sauter, F., Jordis, U., Martinek, P., & Burkart, M. (1990). A new synthesis of benzo[b]naphtho[2,3-d]thiophenes. Journal Für Praktische Chemie, 332(6), 1099–1101. http://hdl.handle.net/20.500.12708/174665 ( reposiTUm)

Jordis, U., Sauter, F., Siddiqi, S. M., Küenburg, B., & Bhattacharya, K. (1990). Synthesis of (1R,4R)- and (1S,4S)-2,5-diazabicyclo[2.2.1]heptanes and their N-substituted derivatives. Synthesis: Journal of Synthetic Organic Chemistry, 10, 925–930. http://hdl.handle.net/20.500.12708/174666 ( reposiTUm)

Hayek, E. W. H., Krenmayr, P., Lohninger, H., Jordis, U., Moche, W., & Sauter, F. (1990). Identification of archaeological and recent wood tar pitches using gas chromatography/mass spectrometry and pattern recognition. Analytical Chemistry, 62(18), 2038–2043. http://hdl.handle.net/20.500.12708/174667 ( reposiTUm)

Sauter, F., Jordis, U., Martinek, P., & Cai, G. (1989). Synthesis of novel quinolone-type drugs. Part 4. Pyrido[3,2,1-gh][1,7]phenanthroline- and benzo[i,j]quinolizinecarboxylic acids. Scientia Pharmaceutica, 57(1), 7–20. http://hdl.handle.net/20.500.12708/174670 ( reposiTUm)

Hayek, E. W. H., Moche, W., Jordis, U., Krenmayr, P., & Sauter, F. (1989). Chemische Analyse von drei bronzezeitlichen Pechfunden aus Dänemark. Acta Archaelogica, 60, 215–227. http://hdl.handle.net/20.500.12708/174642 ( reposiTUm)

Gimbert, Y., Moradpour, A., Bittner, S., & Jordis, U. (1989). Reactions of 2-lithio-1,3-benzodithiole with carbon disulfide: back and forth processes. Tetrahedron Letters, 30(7), 819–822. http://hdl.handle.net/20.500.12708/174671 ( reposiTUm)

Jordis, U., Sauter, F., & Siddiqi, S. M. (1989). Synthesis of (1S,4S)-2-thia-5-azabicyclo[2.2.1]heptane. INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY, 28B(4), 294–296. http://hdl.handle.net/20.500.12708/174669 ( reposiTUm)

Rudolf, M., & Jordis, U. (1989). Simulation of proton- and carbon-13-NMR spectra of aromatic compounds using a personal computer. Chemometrics and Intelligent Laboratory Systems, 5(4), 323–327. http://hdl.handle.net/20.500.12708/174673 ( reposiTUm)

Hayek, E. W. H., Jordis, U., Moche, W., & Sauter, F. (1989). A bicentennial of betulin. Phytochemistry, 28(9), 2229–2242. http://hdl.handle.net/20.500.12708/174672 ( reposiTUm)

Jordis, U., & Varmuza, K. (1988). PC-software for chemists. Österreichische Chemie Zeitschrift, 89(3), 52–58. http://hdl.handle.net/20.500.12708/174678 ( reposiTUm)

Daly, C. M., Iddon, B., Suschitzky, H., Jordis, U., & Sauter, F. (1988). Synthesis of novel 2,3-dihydro-8H-thieno[2,3-d]azepines and 1,2,3,4-tetrahydro-1H-3-benzazepines via photolysis of 6-azido-2,3-dihydrobenzo[b]thiophene and 6-azido-1,2,3,4-tetrahydronaphthalene. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry, 7, 1933–1938. http://hdl.handle.net/20.500.12708/174676 ( reposiTUm)

Jordis, U., Sauter, F., Rudolf, M., & Cai, G. (1988). Syntheses of novel quinolone chemotherapeutics. I. Pyridoquinolines and pyridophenanthrolines as derivatives of “lin-benzo-nalidixic acid.” Monatshefte Für Chemie - Chemical Monthly, 119(6–7), 761–780. http://hdl.handle.net/20.500.12708/174675 ( reposiTUm)

Sauter, F., Jordis, U., & Tanyolac, S. (1988). Synthesis of novel quinolone drugs. Part 3. Thieno[2,3-f]quinolinecarboxylic acids. Scientia Pharmaceutica, 56(2), 73–80. http://hdl.handle.net/20.500.12708/174679 ( reposiTUm)

Jordis, U. (1988). On the mechanism of the reduction of 1,3-benzodithiole-2-thione. Monatshefte Für Chemie - Chemical Monthly, 119(10), 1179–1184. http://hdl.handle.net/20.500.12708/174674 ( reposiTUm)

Sauter, F., Jordis, U., Tanyolac, S., & Martinek, P. (1988). Novel quinolone chemotherapeutics. II. Thieno[3,2-g]quinoline- and [1]benzothieno[5,6,7-ij]quinolizinecarboxylic acids. Archiv Der Pharmazie, 321(4), 241–246. http://hdl.handle.net/20.500.12708/174677 ( reposiTUm)

Sauter, F., Hayek, E. W. H., Moche, W., & Jordis, U. (1987). Identification of betulin in archaeological tar. ZEITSCHRIFT FUR NATURFORSCHUNG SECTION C-A JOURNAL OF BIOSCIENCES, 42(11–12), 1151–1152. http://hdl.handle.net/20.500.12708/174680 ( reposiTUm)

Jordis, U., Sauter, F., & Siddiqi, S. M. (1986). 7,9-Dideaza-9-thiaadenines (4-aminothieno[2,3-d]pyrimidines) as potential anticytokinins). Vestnik Slovenskega Kemijskega Drustva, 33(3), 217–238. http://hdl.handle.net/20.500.12708/174683 ( reposiTUm)

Sauter, F., Jordis, U., & Siddiqi, S. M. (1986). Alkylation of 4-amino-3-mercapto-1,2,4-triazin-5(4H)-ones and oxidation of the products. Journal of Chemical Research, Synopses, 9, 320–321. http://hdl.handle.net/20.500.12708/174682 ( reposiTUm)

Doad, G. J. S., Jordis, U., Rudolf, M., & Sauter, F. (1986). Cyclophilic reactions of allene-1,3-dicarboxylic esters. Part 5. New preparations of quinolones. Journal of Chemical Research, Synopses, 11, 410–411. http://hdl.handle.net/20.500.12708/174685 ( reposiTUm)

Jordis, U. (1986). Hydride reduction of 1,3-benzodithiole-2-thiones and selenones. Journal of Chemical Research, Synopses, 11, 432. http://hdl.handle.net/20.500.12708/174684 ( reposiTUm)

Jordis, U. (1986). Synthesis of dithiooxolinic acid. Monatshefte Für Chemie - Chemical Monthly, 117(11), 1339–1342. http://hdl.handle.net/20.500.12708/174681 ( reposiTUm)

Jordis, U. (1985). Reduktion von Trithiocarbonaten und Anwendung zur Synthese von "Thio-oxolinsäure. Scientia Pharmaceutica, 53(2), 78. http://hdl.handle.net/20.500.12708/174698 ( reposiTUm)

Jordis, U., & Rudolf, M. (1984). Conversion of cyclic trithiocarbonates to thioacetals, including 1,3-dithiane, by reduction with diisobutylaluminum hydride (DIBAL). Phosphorus and Sulfur and the Related Elements, 19(3), 279–283. http://hdl.handle.net/20.500.12708/174693 ( reposiTUm)

Sauter, F., Jordis, U., & Cai, G. (1983). Dehydrogenation of 2-ethylbenzenethiols: improved synthesis of benzo[b]thiophenes. Journal of Chemical Research, Synopses, 11, 276. http://hdl.handle.net/20.500.12708/174695 ( reposiTUm)

Daly, C. M., Iddon, B., Suschitzky, H., Jordis, U., & Sauter, F. (1983). Synthesis of novel 8H-thieno[2,3-d]azepines by photolysis of 6-azido-2,3-dihydrobenzo[b]thiophene. Tetrahedron Letters, 24(46), 5147–5150. http://hdl.handle.net/20.500.12708/174694 ( reposiTUm)

Jordis, U., & Oberhauser, O. (1982). Status of computer search of the chemical literature: (partial) structural research with GREMAS, DARC, and CAS ONLINE. Österreichische Chemie Zeitschrift, 83(12), 311–314. http://hdl.handle.net/20.500.12708/174697 ( reposiTUm)

Sauter, F., Stanetty, P., Jordis, U., Hetzl, E., & Konstantinou, D. (1982). A novel type of analgesic antiphlogistic. II: Benzo[b]thienylpiperazines. Archiv Der Pharmazie, 315(11), 912–918. http://hdl.handle.net/20.500.12708/174696 ( reposiTUm)

Sauter, F., Jordis, U., Stanetty, P., Huettner, G., & Otruba, L. (1981). A new type of analgesic antiphlogistics. I: 2,3-Dihydro-2-phenylbenzo[b]thiophene 1,1-dioxides with basic substituents. Archiv Der Pharmazie, 314(6), 567–572. http://hdl.handle.net/20.500.12708/174692 ( reposiTUm)

Evans, D. L., Minster, D. K., Jordis, U., Hecht, S. M., Mazzu, A. L., & Meyers, A. I. (1979). Nickel peroxide dehydrogenation of oxygen-, sulfur-, and nitrogen-containing heterocycles. Journal of Organic Chemistry, 44(4), 497–501. http://hdl.handle.net/20.500.12708/174691 ( reposiTUm)

Minster, D. K., Jordis, U., Evans, D. L., & Hecht, S. M. (1978). Thiazoles from cysteinyl peptides. Journal of Organic Chemistry, 43(8), 1624–1626. http://hdl.handle.net/20.500.12708/174690 ( reposiTUm)

Sauter, F., Jordis, U., & Stanetty, P. (1977). Synthesis of substituted phenylhydrazines as open-chain analogs of herbicidal pyridazinones. Journal of Chemical Research, Synopses, 7, 187. http://hdl.handle.net/20.500.12708/174688 ( reposiTUm)

Sauter, F., & Jordis, U. (1977). Novel 1,3-diarylpyrazolines and pyrazolo[3,4-d]pyridazines. Organic Preparations and Procedures International: The New Journal for Organic Synthesis, 9(1), 45–48. http://hdl.handle.net/20.500.12708/174689 ( reposiTUm)

Sauter, F., Stanetty, P., & Jordis, U. (1977). New 3-aminoquinazolinones. Archiv Der Pharmazie, 310(8), 680–682. http://hdl.handle.net/20.500.12708/174687 ( reposiTUm)

McGowan, D. A., Jordis, U., Minster, D. K., & Hecht, S. M. (1977). A biomimetic synthesis of the bithiazole moiety of bleomycin. Journal of the American Chemical Society, 99(24), 8078–8079. http://hdl.handle.net/20.500.12708/174686 ( reposiTUm)

Sauter, F., Bueyuek, G., & Jordis, U. (1974). Synthesis of 1H-[1]benzothieno [3,2-c] pyrazoles. Neurochemistry, 105(4), 869–876. http://hdl.handle.net/20.500.12708/175843 ( reposiTUm)

Sauter, F., & Jordis, U. (1974). Synthesis of 2- and 3-phenylbenzo[b]thiophene 1,1-dioxide with basic substituents. Monatshefte Für Chemie - Chemical Monthly, 105(6), 1252–1257. http://hdl.handle.net/20.500.12708/175844 ( reposiTUm)

Martinek, P., Ortega, C., Lee, V. J., Jordis, U., & Upadhyay, J. (2010). Linear Extended Quinolones: Synthesis and Antibacterial Activity of Lin-Benzo-Ciprofloxacin. In XXIVth European Colloquium on Heterocyclic Chemistry (p. PO-40). http://hdl.handle.net/20.500.12708/46879 ( reposiTUm)

Khan, F. A., Rabong, C., Phopase, J., & Jordis, U. (2010). Triazepiene-Triones as Cyclized NXO-Peptides. In XXIVth European Colloquium on Heterocyclic Chemistry (p. PO-105). http://hdl.handle.net/20.500.12708/46880 ( reposiTUm)

Patil, A., Beldar, S. V., Knesl, P., & Jordis, U. (2010). Synthesis of A Landiolol Metabolite. In XXIVth European Colloquium on Heterocyclic Chemistry (p. PO-39). http://hdl.handle.net/20.500.12708/46878 ( reposiTUm)

Jordis, U., Knesl, P., Phopase, J., Manvar, D., Maghazehi, M., & Maelicke, A. (2008). Insights into mechanism of action lead to a new generation of galanthamine-deried drugs. In Abstracts from the XXth International Symposium on Medicinal Chemistry (p. 273). Thomson Reuters. http://hdl.handle.net/20.500.12708/46088 ( reposiTUm)

Jordis, U., & Phopase, J. (2008). Novel NXO-Building Blocks for Peptide Backbone Modification and Preparation of New Class Pseudopeptides. In 12th ISCB Conference (ISCBC-2008). International Conference on the Interface of Chemistry-Biology in Biomedical Research - ABSTRACTS. (p. 69). http://hdl.handle.net/20.500.12708/46161 ( reposiTUm)

Jordis, U., Knesl, P., & Puterova, Z. (2007). The Synthesis of Deuterated Tolperisone and Tolperisone Metabolites. In JMMC 2007 - Book of Abstracts (p. 113). Farmacevtski Vestnik. http://hdl.handle.net/20.500.12708/45735 ( reposiTUm)

Jordis, U. (2007). The integration of software and databases into the daily workflow of a medicinal chemist. In IQPC Fosused Compound Libraries 2007. IQPC Fosused Compound Libraries 2007, Frankfurt, EU. IQPC GmbH, Berlin. http://hdl.handle.net/20.500.12708/45819 ( reposiTUm)

Jordis, U., Beseda, I., & Manvar, D. (2007). Improved O-Axylcarnitine Derivates. In JMMC 2007 - Book of Abstracts (p. 113). Farmacevtski Vestnik. http://hdl.handle.net/20.500.12708/45734 ( reposiTUm)

Jordis, U., Knesl, P., & Yousefí, B. H. (2006). Synthesis of (-)- and (+)-8-fluoro-galanthamin. In Scientia Pharmaceutica 2006 (p. 60). Scientia Pharmaceutica. http://hdl.handle.net/20.500.12708/45707 ( reposiTUm)

Jordis, U. (2006). How to use software and integrate databases in the daily practice of heterocyclic chemist. In The Chemistry and Biological Activity of Synthetic and Natural Compounds Volume 1 Nitrogen-Containing Heterocycles (pp. 67–71). http://hdl.handle.net/20.500.12708/45473 ( reposiTUm)

Yousefí, B. H., & Jordis, U. (2006). (4-Isobutyl-phenyl)-acetic acid (Ibufenac) Microwave-Assisted and Conventional Synthesis. In 10th Electronic Conference on Synthetic Organic Chemistry (p. 7). http://hdl.handle.net/20.500.12708/45551 ( reposiTUm)

Yousefí, B. H., & Jordis, U. (2006). New Synthesis of 4,4’-Diethylaminoethoxyhexestrol dihydrochloride (Coralgil) and scaling up to multi-grams scale. In 10th Electronic Conference on Synthetic Organic Chemistry (p. 4). http://hdl.handle.net/20.500.12708/45550 ( reposiTUm)

Jordis, U., Treu, M., & Hirnschall, M. (2006). SYNTHESIS AND SAR OF SECOND GENERATION GALANTHAMINE-TYPE ANTI-ALZHEIMER DRUGS. In 1st European Chemistry Congress - 27-31 August 2006 - Budapest, Hungary. 1st European Chemistry Congress, Budapest, Hungary, EU. http://hdl.handle.net/20.500.12708/45560 ( reposiTUm)

Gerdes, K., Jordis, U., Kappe, C., & Kremser, J. (2005). DEVELOPMENT OF MULTI-GRAM SCALE MICROWAVE ASSISTED ORGANIC SYNTHESIS (MAOS): SUZUKI COUPLING TOWARDS 2,4-DIMETHYL-8-[2’-(2H-TETRAZOL-5-YL)-BIPHENYL-4-YLMETHYL]-5,8-DIHYDRO-6H-PYRIDO[2,3-D]PYRIMIDIN-7-ONE (TASOSARTAN). In 9th International Electronic Conference on Synthetic Organic Chemistry. 9th International Electronic Conference on Synthetic Organic Chemistry (ECSOC9), Internet, Austria. http://hdl.handle.net/20.500.12708/45246 ( reposiTUm)

Knesl, P., & Jordis, U. (2005). Butorphanol metabolites: Synthesis of cis- and trans- 3,14-dihydroxy-N-(3’-hydroxycyclobutylmethyl) morphinan. In 9th International Electronic Conference on Synthetic Organic Chemistry (ECSOC9). 9th International Electronic Conference on Synthetic Organic Chemistry (ECSOC9), Internet, Austria. http://hdl.handle.net/20.500.12708/45247 ( reposiTUm)

Jordis, U. (2005). The integration of databases and software into the day-to-day practice of a hetrocyclic chemist. In 11th Blue Danube Symposium on Heterocyclic Chemistry - Book of Abstracts. 11#^{th} Blue Danube Symposium on Heterocyclic Chemistry, Brünn, Tschechien, Austria. Masaryk University in Brno. http://hdl.handle.net/20.500.12708/45242 ( reposiTUm)

Knesl, P., & Jordis, U. (2005). SYNTHESIS OF cis AND trans-3’-HYDROXYBUTORPHANOL. In 11th Blue Danube Symposium on Heterocyclic Chemistry - Book of Abstracts. 11#^{th} Blue Danube Symposium on Heterocyclic Chemistry, Brünn, Tschechien, Austria. Masaryk University in Brno. http://hdl.handle.net/20.500.12708/45241 ( reposiTUm)

Gerdes, K., Kremser, J., Kappe, C., & Jordis, U. (2005). Synthesis of 2,4-Dimethyl-8-[2’-(2H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-5,8-dihydro-6H -pyrido[2,3-d]pyrimidin-7-one (Tasosartan) and Application of Microwave Assisted Organic Synthesis. In Electronical Conference Book of the First Austrian-German-Italian Meeting of Organic Chemistry Vienna 2005. First Austrian-German-Italian Meeting of Organic Chemistry, Wien, Austria. http://hdl.handle.net/20.500.12708/45122 ( reposiTUm)

Jordis, U., Knesl, P., Röseling, D., & Lee, H. (2005). Improved Synthesis of Tandutinib, Erlotinib, and Gefitinib. In Abstracts of Scientific Papers (p. 121). http://hdl.handle.net/20.500.12708/45093 ( reposiTUm)

Knesl, P., & Jordis, U. (2005). New Challanges with Old Drugs: Sulfapyridine Metabolites. In Abstract od Scientific Papers (p. 223). http://hdl.handle.net/20.500.12708/45092 ( reposiTUm)

Jordis, U. (2003). Synthesis of the Rescaffolded Galanthamine Analogues. In 16th Lakeland Heterocyclic Symposium. 15th Lakeland Heterocyclic Symposium, Grasmere, Großbritannien, Austria. http://hdl.handle.net/20.500.12708/45074 ( reposiTUm)

Jordis, U., Cvitkovich, B., Czollner, L., Fröhlich, J., Küenburg, B., Mereiter, K., & Rizzi, A. (1998). 150 Years of Pasteur’s Classic Tartaric Acid Resolution: How to use Conglomerates for the Resolution and Conversion of Enantiomers of Pharmaceutical Relevance. In 10th International Symposium on Chiral Discrimination - Book of Abstracts. 10th International Symposium on Chiral Discrimination, Wien, Österrecih, Austria. http://hdl.handle.net/20.500.12708/45145 ( reposiTUm)

Jordis, U., Rizzi, A., & Grohmann, F. (1998). Molecular imprinted polymers for the chiral separation of pharmaceutically relevant heterocycles: first results of the separation of the anti-Alzheimer drug galanthamine. In ECHET98 (p. 3). Electronic Conference on Heterocyclic Chemistry (ECHET98). http://hdl.handle.net/20.500.12708/45147 ( reposiTUm)

Jordis, U., Sauter, F., & Martinek, P. (1997). Who can model new quinolone-type heterocycles as potential antibacterials? Synthesis of thieno[2’,3’:4,5]thieno [3,2-b]pyridone-3-carboxylic acids. In Electronic Conference on Heterocyclic Chemistry-Proceedings. Electronic Conference on Heterocyclic Chemistry (ECHET96), Austria. Electronic Conference on Heterocyclic Chemistry (ECHET96). http://hdl.handle.net/20.500.12708/45149 ( reposiTUm)

Varmuza, K., Jordis, U., & Wolf, G. (1997). Database mining for heterocycles: are structures of small heterocycles generated by a computer program present in databases? In Electronic Conference on Heterocyclic Chemistry-Proceedings. Electronic Conference on Heterocyclic Chemistry (ECHET96), Austria. Electronic Conference on Heterocyclic Chemistry (ECHET96). http://hdl.handle.net/20.500.12708/45148 ( reposiTUm)

Sauter, F., Jordis, U., & Martinek, P. (1997). [1]Benzothieno[3,2-b]pyridone -3- carboxylic acids as potential antibacterials. In Electronic Conference on Heterocyclic Chemistry-Proceedings. Electronic Conference on Heterocyclic Chemistry (ECHET96), Austria. Electronic Conference on Heterocyclic Chemistry (ECHET96). http://hdl.handle.net/20.500.12708/45150 ( reposiTUm)

Jordis, U., & Küenburg, B. (1997). Chiral bridged piperazines: synthesis of (1S,4S)-2,5-diazabicyclo[2.2.2]octane. In Electronic Conference on Heterocyclic Chemistry-Proceedings. Electronic Conference on Heterocyclic Chemistry (ECHET96), Austria. Electronic Conference on Heterocyclic Chemistry (ECHET96). http://hdl.handle.net/20.500.12708/45151 ( reposiTUm)

Jordis, U. (1997). Substance and reaction databases: case studies for the perplexed heterocyclic chemist. In Electronic Conference on Heterocyclic Chemistry (ECHECT96)- Proceedings. Electronic Conference on Heterocyclic Chemistry (ECHECT96), Austria. Electronic Conference on Heterocyclic Chemistry (ECHET96). http://hdl.handle.net/20.500.12708/45178 ( reposiTUm)

Sauter, F., Jordis, U., & Rudolf, M. (1985). Heterocyclisch anellierte Pyridoncarbonsäurederivate als potentielle Chemotherapeutika. In 6.Österreichische Chemietage und LAVAC ´85 - Abstracts (p. 19). http://hdl.handle.net/20.500.12708/45146 ( reposiTUm)

Jordis, U. (2007). Chemistry - Education and Technology Transfer. In E. Müllner (Ed.), Higher Education Kooperationen Austria/India (p. 17). Österreichischer Austauschdienst. http://hdl.handle.net/20.500.12708/25316 ( reposiTUm)

Jordis, U. (2011). Freude an der Chemie. Experimentalvorlesung zur Frage “Was machen ChemikerInnen?” Volkshochschule Meidling, Wien, Austria. http://hdl.handle.net/20.500.12708/98348 ( reposiTUm)

Jordis, U. (2011). Datebases, Search Engines and Software. An Update for the Synthetic and Medicinal Chemist. 3rd International Workshop on Databases, Search Engines and Software., Rajkot, Indien, Non-EU. http://hdl.handle.net/20.500.12708/98472 ( reposiTUm)

Jordis, U., Czollner, L., Stanetty, C., Odermatt, A., Kosma, P., & Classen-Houben, D. (2011). Synthesis and SAR of new glycyrrhetinic acid derivated derivatives sa 11beta-hydroxysteroid dehyrogenase inhibitors. 15th ISCBC-2011 (International Conference on Bridging Gaps in Discovery and Development, Rajkot (Gujarat) Indien, Non-EU. http://hdl.handle.net/20.500.12708/98473 ( reposiTUm)

Jordis, U., Martinek, P., Ortega, C., Lee, V. J., & Rajyaguru, C. (2011). Linear Extended Quinolones: Synthesis and Antibacterial Activity of Lin-Benzo-Ciprofloxacin. 15th ISCBC-2011 (International Conference on Bridging Gaps in Discovery and Development, Rajkot (Gujarat) Indien, Non-EU. http://hdl.handle.net/20.500.12708/98474 ( reposiTUm)

Jordis, U. (2011). Databases, SearchEngines and Software: An Update for the Synthetic and Medicinal Chemist. Sinhagad College of Pharmacy, Pune, Pune, Indien, Non-EU. http://hdl.handle.net/20.500.12708/98478 ( reposiTUm)

Jordis, U. (2011). Recent Developments in Databases and Software for Synthesis Planning. Acoris Research Ltd., Maharashtra, Indien, Non-EU. http://hdl.handle.net/20.500.12708/98477 ( reposiTUm)

Jordis, U. (2011). The current Status of Alzheimer Therapeutics and the role of Galanthamine. Pune University National Chemistry Laboratory, Pune, Pune, Indien, Non-EU. http://hdl.handle.net/20.500.12708/98476 ( reposiTUm)

Jordis, U. (2011). The current Status of Alzheimer Therapeutics and the role of Galanthamine. University of Pune, Pune, Indien, Non-EU. http://hdl.handle.net/20.500.12708/98475 ( reposiTUm)

Jordis, U. (2011). AUSTROMOL - The Austrian Repository of Molecular Diversity. Austrodrugs, Ce-M-M- Research Center for Molecular Medicine of the Austrian Academy of Sciences, Austria. http://hdl.handle.net/20.500.12708/98487 ( reposiTUm)

Jordis, U. (2011). The Daily Workflow of a Medicinal/Organic Chemist to Manage the Personal Information Need. ONLINE Information, London, EU. http://hdl.handle.net/20.500.12708/98601 ( reposiTUm)

Jordis, U. (2010). Freude an der Chemie. Experimentalvorlesung zur Frage “Was machen ChemikerInnen?” Volkshochschule Favoriten, Wien, Austria. http://hdl.handle.net/20.500.12708/98347 ( reposiTUm)

Beldar, S. V., & Jordis, U. (2010). Antiviral Pyrazinecarboxamides Including Improved Synthesis of Favipiravir. ICOS-18; 18th International Conference on Organic Synthesis, Bergen / Norwegen, Non-EU. http://hdl.handle.net/20.500.12708/98324 ( reposiTUm)

Jordis, U. (2010). Magic Chemistry: Die Freude am Experiment. Volkshochschule Wien West, Wien, Austria. http://hdl.handle.net/20.500.12708/98279 ( reposiTUm)

Czollner, L., Beseda, I., Jordis, U., Stanetty, C., Amer, H., Ruiz-Ruiz, C., Kosma, P., & Classen-Houben, D. (2009). Ugi reactions of tertiary carboxylic acids: Combinatorial synthesis of glycyrrhetinic acid derivatives. 13rd International Electronic Conference on Synthetic Organic Chemistry (ECSOC-13), elektronische Konferenz, EU. http://hdl.handle.net/20.500.12708/98086 ( reposiTUm)

Khan, F. A., Phopase, J., & Jordis, U. (2009). Surprise in the Lithium Hydroxide Hydrolysis of a NXO-Compound. 13rd International Electronic Conference on Synthetic Organic Chemistry (ECSOC-13), elektronische Konferenz, EU. http://hdl.handle.net/20.500.12708/98087 ( reposiTUm)

Gaware, R., & Jordis, U. (2009). Selective Mono-Boc-Protection of Bispidine. 13rd International Electronic Conference on Synthetic Organic Chemistry (ECSOC-13), elektronische Konferenz, EU. http://hdl.handle.net/20.500.12708/98089 ( reposiTUm)

Beldar, S. V., & Jordis, U. (2009). Synthetic studies towards the antiviral pyrazine derivative T-705. 13rd International Electronic Conference on Synthetic Organic Chemistry (ECSOC-13), elektronische Konferenz, EU. http://hdl.handle.net/20.500.12708/98088 ( reposiTUm)

Stanetty, C., Amer, H., Beseda, I., Czollner, L., Classen-Houben, D., Wolkerstorfer, A., Mutzl, M., Szolar, O., Jordis, U., & Kosma, P. (2009). Synthesis of Thioglucuronide-Derivatives of Glycyrrhizin. 15th European Carbohydrate Symposium (Eurocarb 15), Wien, Austria. http://hdl.handle.net/20.500.12708/98278 ( reposiTUm)

Jordis, U. (2008). Integration of Electronic Notebook Software into the Workflow of an Academic Research Group. Symyx Global Symposium - “R&D Integration Success,” Prag, EU. http://hdl.handle.net/20.500.12708/97822 ( reposiTUm)

Jordis, U. (2008). The Digital Global Village: Literaturdatenbanken im täglichen Workflow eines Naturwissenschaftlers. Bibliothekars-Forum 2008, Wien, Austria. http://hdl.handle.net/20.500.12708/97821 ( reposiTUm)

Jordis, U. (2008). The Digital Global Village: Literaturdatenbanken im täglichen Workflow eines Naturwissenschaftlers. Elsevier Bibliothekars-Forum 2008: “Welchen Mehr-Wert hat digitale Information für Ihre Bibliothek?,” Berlin, EU. http://hdl.handle.net/20.500.12708/97820 ( reposiTUm)

Classen-Houben, D., Beseda, I., Schuster, D., Odermatt, A., Czollner, L., Shah, P., Amer, H., Stanetty, C., Ruiz-Ruiz, C., Kosma, P., Wolber, G., Jordis, U., & Küenburg, B. (2008). Differences in binding of 18A- and 18B-glycyrrhetinic acid to 11B-hydroxysteroid dehydrogenase. 18th International Symposium of the Journal of Steroid Biochemistry & Molecular Biology, Seefeld, Austria. http://hdl.handle.net/20.500.12708/97828 ( reposiTUm)

Phopase, J., Jordis, U., & Ayoub, M. (2008). NXO-Modified Amino Acids: Novel Building Blocks for Peptidomimetics. TIDES 2008 - Olingonucleotide and Peptide tchnology and Product Development, Las Vegas, USA, Non-EU. http://hdl.handle.net/20.500.12708/97829 ( reposiTUm)

Jordis, U., & Bhujbal, M. (2008). Management and use of chemistry databases and patent literature. Three days workshop on management and use of chemistry databases and patent literature. A short course for academic and industrial synthetic organic chemists., Rajkot, Non-EU. http://hdl.handle.net/20.500.12708/97808 ( reposiTUm)

Jordis, U. (2008). The Digital Global Village: Literaturdatenbanken im täglichen Workflow eines Naturwissenschaftlers. Elsevier Bibliothekars-Forum 2008: “Welchen Mehr-Wert hat digitale Information für Ihre Bibliothek?,” Berlin, EU. http://hdl.handle.net/20.500.12708/97807 ( reposiTUm)

Jordis, U. (2008). Hands-on problem solving. Management and use of chemistry databases and patent literature. Three days workshop on management and use of chemistry databases and patent literature. A short course for academic and industrial synthetic organic chemists., Rajkot, Non-EU. http://hdl.handle.net/20.500.12708/97815 ( reposiTUm)

Jordis, U. (2007). NXO-Modified Amino acids as Novel Building Blocks for Peptidomimetics. Fa. SENN, Dielsdorf, Schweiz, Non-EU. http://hdl.handle.net/20.500.12708/97465 ( reposiTUm)

Jordis, U. (2006). The Galanthamin Story: From Total Systems to Alzheimer Drugs. Claris Lifesciences Ltd., Ahmedabad, Non-EU. http://hdl.handle.net/20.500.12708/97437 ( reposiTUm)

Jordis, U. (2006). The Importance of the Digital Library for Science and Education. Amity University, Lucknow, India, Non-EU. http://hdl.handle.net/20.500.12708/97438 ( reposiTUm)

Jordis, U., Valla, C., & Rabong, C. (2006). T-Reactions With Chiral Amines. III International Conference on The Chemistry and Biological Activity of Nitrogen-Containing Heterocycles, Chernogolovka, Moscow, Russia, Non-EU. http://hdl.handle.net/20.500.12708/97432 ( reposiTUm)

Jordis, U. (2006). Synthesis and SAR of Second Generation Galanthamine-Type Anti-Alzheimer Drugs. 10th International Conference of ISCB, Lucknow, India, Non-EU. http://hdl.handle.net/20.500.12708/97433 ( reposiTUm)

Jordis, U., & Manvar, D. (2006). Synthesis of Acylcarnitine Derivatives. 10th International Conference of ISCB, Lucknow, India, Non-EU. http://hdl.handle.net/20.500.12708/97434 ( reposiTUm)

Jordis, U. (2006). Die Gewald-Reaktion: Bedeutung und Auswirkung einer in Dresden entstandenen Entdeckung. GDCh Kolloquium - Dresden, Technische Universität Dresden, EU. http://hdl.handle.net/20.500.12708/97430 ( reposiTUm)

Jordis, U. (2006). Synthesis of Second-Generation Galanthamine-type Anti-Alzheimer Drugs. ALTANA Pharma Private Limited, Mumbai, Indien, Non-EU. http://hdl.handle.net/20.500.12708/97429 ( reposiTUm)

Jordis, U. (2006). Integration of software and databases into the day-to-day practice of an organic chemist. Saurashtra University, Rajkot, Indien, Non-EU. http://hdl.handle.net/20.500.12708/97431 ( reposiTUm)

Jordis, U. (2006). Lessons and Tools in Upscaling and Drug Development: Second Generation Galanthamine-Type Anti-Alzheimer Drugs. Unimark Remedies Ltd., Ahmedabad, Non-EU. http://hdl.handle.net/20.500.12708/97435 ( reposiTUm)

Jordis, U. (2006). Second Generation Galanthamine-Type Anti-Alzheimer Drugs and the Digital Library. Nirma University, Ahmedabad, Non-EU. http://hdl.handle.net/20.500.12708/97436 ( reposiTUm)

Jordis, U. (2006). Digitale Bibliothek: Informationserschließung mit MDL Datenbanken unter DiscoveryGate. Chemiehörsal der TU, Wien, Austria. http://hdl.handle.net/20.500.12708/97461 ( reposiTUm)

Jordis, U. (2005). Experiences with DiscoveryGate in Academia. Elsevier MDL 2005 European User´s Group Meeting, Prague, Czech Republic, EU. http://hdl.handle.net/20.500.12708/97073 ( reposiTUm)

Jordis, U. (2005). Molecular Architecture to Prepare Structures with Desired Properties. European ECheminfo InterAction Meeting 2005, Basel, Schweiz, EU. http://hdl.handle.net/20.500.12708/97074 ( reposiTUm)

Marquardt, U., Seipelt, J., & Jordis, U. (2005). Solid phase supported synthesis of alkyl dithiocarbamates. Joint Meeting on Medicinal Chemistry, Budapest, Hungary, EU. http://hdl.handle.net/20.500.12708/96819 ( reposiTUm)

Gerdes, K., Kremser, J., Kappe, C., & Jordis, U. (2005). Synthesis of 2,4-dimethyl-8-[2’-(2H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-5,8-dihydro-6H-pyrido[2,3-D]pyrimidin-7-one (tasosartan) and application of microwave assisted organic synthesis. Joint Meeting on Medicinal Chemistry, Budapest, Hungary, EU. http://hdl.handle.net/20.500.12708/96821 ( reposiTUm)

Knesl, P., & Jordis, U. (2005). Synthesis of deuterated analogs of pharmaceuticals. Joint Meeting on Medicinal Chemistry, Budapest, Hungary, EU. http://hdl.handle.net/20.500.12708/96820 ( reposiTUm)

Skubak, J., Phopase, J., & Jordis, U. (2005). Microwave Assisted and Conventional Mono Aryl Substitution of Diazabicycloalkanes by Encapsulated Palladium Coupling. Joint Meeting on Medicinal Chemistry, Budapest, Hungary, EU. http://hdl.handle.net/20.500.12708/96818 ( reposiTUm)

Jordis, U. (2003). Synthese von Galanthamin Analoga: Kombinatorische Chemie und Rescaffolding. Tagung Mainz, Universität Mainz, Austria. http://hdl.handle.net/20.500.12708/96225 ( reposiTUm)

Kos, A., Toman, D., Poroikov, V. V., Jordis, U., & Knuuttila, T. (2002). Finding new acetylcholinesterase inhibitors using biological profiles. Molecular Modelling in Life Science And Materials Science, Frankfurt/Main, Austria. http://hdl.handle.net/20.500.12708/95795 ( reposiTUm)

Jordis, U. (2002). Chemische Synthese im 21. Jahrhundert. Techniker - Cercle, Wien, Austria. http://hdl.handle.net/20.500.12708/95787 ( reposiTUm)

Jordis, U. (2002). Zitronenbatterie, Kaltes Licht und Blaukrautsaft. University meets Public (VHS), Wien, Austria. http://hdl.handle.net/20.500.12708/95785 ( reposiTUm)

Jordis, U. (2002). Zitronenbatterie, Kaltes Licht und Blaukrautsaft. University meets Public (VHS), Wien, Austria. http://hdl.handle.net/20.500.12708/95784 ( reposiTUm)

Jordis, U. (2002). Zitronenbatterie, Kaltes Licht und Blaukrautsaft. University meets Public (VHS), Wien, Austria. http://hdl.handle.net/20.500.12708/95786 ( reposiTUm)

Hirnschall, M., & Jordis, U. (2002). Synthesis and stereoselective dealkylation  of N-chiral quarternary N-alkyl galanthaminium halides. 10. Österreichische Chemietage, Linz, Austria. http://hdl.handle.net/20.500.12708/95794 ( reposiTUm)

Fröhlich, J., Jordis, U., Hemetsberger, M., Czollner, L., & Küenburg, B. (2001). A Novel Alzheimer Therapeutic: Galanthamine, An Amaryllidaceae Alkaloid -Its Technical Synthesis And Novel Derivatives. 4#^{th} National Meeting of Organic Chemistry, Coimbra, Porzugal, Austria. http://hdl.handle.net/20.500.12708/95992 ( reposiTUm)

Jordis, U. (2001). The Integration of Chemical Databases into the Daily Work-Flow of a Research Chemist. Technische Universität Bratislava, Bratislava, Slovakei, Austria. http://hdl.handle.net/20.500.12708/96022 ( reposiTUm)

Jordis, U. (2001). Synthesis of Galanthamine Analogs: Classical and Combinatorial Approaches. Firma Carbogen, Aarau, Austria. http://hdl.handle.net/20.500.12708/96024 ( reposiTUm)

Jordis, U. (2001). Synthesis of Galanthamine Analogs: Classical and Combinatorial Approaches. Firma Morphochem, München, Deutschland, Austria. http://hdl.handle.net/20.500.12708/96023 ( reposiTUm)

Jordis, U. (2001). A simple and Economic Design for a Personal Synthesizer. First Symposium of the European Society for Combinatorial Science (Eurocombi-1), Budapest, Ungarn, Austria. http://hdl.handle.net/20.500.12708/96027 ( reposiTUm)

Jordis, U. (2001). An Improved Design of a Parallel Synthesis Block. First Symposium of the European Society for Combinatorial Science (Eurocombi-1), Budapest, Ungarn, Austria. http://hdl.handle.net/20.500.12708/96028 ( reposiTUm)

Jordis, U., & Kühn, C. (2001). Combinatorial Modifications of Natural Products: Galanthamine as Scaffold for Second Generation Anti-Alzheimer Compounds. First Symposium of the European Society for Combinatorial Science (Eurocombi-1), Budapest, Ungarn, Austria. http://hdl.handle.net/20.500.12708/96055 ( reposiTUm)

Jordis, U., Treu, M., & Hirnschall, M. (2001). Combinatorial Synthesis of Diazo Dyes: A Student Experiment. First Symposium of the European Society for Combinatorial Science (Eurocombi-1), Budapest, Ungarn, Austria. http://hdl.handle.net/20.500.12708/96026 ( reposiTUm)

Hirnschall, M., & Jordis, U. (2001). Chiralität am Stickstoff: Stereoselktive Dealkylierung von N-Alkyl-Galanthaminium Salzen. Sigma-Aldrich Symposium für Synthetische Chemie, Burg Schlaining, Österreich, Austria. http://hdl.handle.net/20.500.12708/96025 ( reposiTUm)

Jordis, U., & Hirnschall, M. (2000). Chirality on Nitrogen: Stereoselective Dealkylation of N-Alkyl-Galanthaminium Salts. Gordon Research Conference, Massachusatts, USA, Austria. http://hdl.handle.net/20.500.12708/96271 ( reposiTUm)

Jordis, U. (1985). Reduktion von Trithiocarbonaten und Anwendung zur Synthese von “Thio-oxolinsäure.” 5. Wissenschaftliche Tagung der Österreichischen Pharmazeutischen Gesellschaft, Graz, Österreich, Austria. http://hdl.handle.net/20.500.12708/96822 ( reposiTUm)