- ISSN 0010-0765 printed
- ISSN 1212-6950 electronic
1999, Volume 64, Issue 2
Organic, Bioorganic and Medicinal Chemistry
-
pp. 177-189
Renata Toplak, Jurij Svete*, Simona Golič Grdadolnik and Branko Stanovnik* Methyl (Z)-2-[(Benzyloxycarbonyl)amino]-3-dimethyl- aminopropenoate in the Synthesis of Heterocyclic Systems. Synthesis of (Benzyloxycarbonyl)amino Substituted Fused Pyrimidinones -
pp. 190-202
Attila Sápi, József Fetter*, Károly Lempert, Mária Kajtár-Peredy and Gábor Czira Simple and Condensed β-Lactams. Part 32. Base- and Acid-Catalyzed Ring Expansions of 3-Substituted 4-Acetylazetidin-2-ones and Related Compounds -
pp. 203-216
Patricia Bottari, Mary Ann A. Endoma, Tomáš Hudlický*, Ion Ghiviriga and Khalil A. Abboud Intramolecular N-Acyliminium Ion-Olefin Cyclization in the Synthesis of Optically Pure Isoquinoline Derivatives: Control of Stereochemistry and Application to Synthesis of Morphine Alkaloids -
pp. 217-228
Jian Guan, Xiao-Kang Zhu, Arnold Brossi, Yoko Tachibana, Kenneth F. Bastow, Pascal Verdier-Pinard, Ernest Hamel, Andrew T. McPhail and Kuo-Hsiung Lee* Antitumor Agents. 192. Antitubulin Effect and Cytotoxicity of C(7)-Oxygenated Allocolchicinoids -
pp. 229-241
Michal Hocek* and Antonín Holý Perfluoroalkylation of 6-Iodopurines by Trimethyl(perfluoroalkyl)silanes. Synthesis of 6-(Perfluoroalkyl)purine Bases, Nucleosides and Acyclic Nucleotide Analogues -
pp. 242-256
Antonín Holý*, Miloš Buděšínský, Jaroslav Podlaha and Ivana Císařová Synthesis of Quaternary 1-[2-(Phosphonomethoxy)ethyl] Derivatives of 2,4-Diaminopyrimidine and Related Acyclic Nucleotide Analogs -
pp. 257-264
Pavel Hradil*, Jan Vaněček, Jan Hlaváč and Juraj Ševčík Synthesis of 2-Substituted-6,7-dimethoxy- and 6,7,8-Trimethoxy-3-hydroxyquinolin-4(1H)-ones -
pp. 265-287
Libor Dušek*, Jaromír Kaválek and Vojeslav Štěrba Kinetics of Methanolysis of Substituted Benzamide O-(Phenoxycarbonyl)- and O-(Alkoxycarbonyl)oximes Catalyzed by Sodium Methanolate -
pp. 288-298
Abd El-Galil Amr, Osama I. Abd El-Salam, Abd El-Hamid Attia and Ivan Stibor* Synthesis of New Potential Bis-Intercalators Based on Chiral Pyridine-2,6-dicarboxamides -
pp. 299-312
Aldo Andreani*, Alberto Leoni, Alessandra Locatelli, Rita Morigi, Mirella Rambaldi, Jean-Claude Gehret, Serena Traniello, Alessio Cariani and Susanna Spisani Ring-Opened Analogs of Indomethacin Affecting Human Neutrophil Functions -
pp. 313-320
Shahriyar Taghavi-Moghadam, Rüdiger Stumpf, Helmut Fischer and Wolfgang Pfleiderer* Facile Synthesis of 6-Aryl-1,3-dimethyl-5H-pyrimido[4,5-b][1,4]diazepine-2,4(1H,3H)-diones -
pp. 321-328
Róbert Sleziak and Alžbeta Krutošíková* Cycloaddition Reactions of Furo[2,3-b]pyrroles -
pp. 329-347
Eva Klinotová*, Jitka Čermáková, Martin Rejzek, Václav Křeček, Jan Sejbal, Petr Olšovský and Jiří Klinot Reaction of 18β,19β-Epoxylupan-21-one Derivatives with Acids: A Way to 21,22-Disubstituted Lup-18-ene Triterpenoids -
pp. 348-362
Peter Kutschy*, Milan Dzurilla, Mitsuo Takasugi and Adriana Sabová Synthesis of Some Analogs of Indole Phytoalexins Brassinin and Methoxybrassenin B and Their Positional Isomers -
pp. 363-376
Stanislav Rádl*, Wieland Hafner, Petr Hezký, Ivan Krejčí, Jan Proška and Jan Taimr Molecular Modification of Anpirtoline, a Non-Opioid Centrally Acting Analgesic -
pp. 377-388
Stanislav Rádl*, Wieland Hafner, Petr Hezký, Ivan Krejčí, Jan Proška and Josef Hájíček Synthesis and Antinociceptive Activity of Some 3-Chlorophenyl- and 6-Chloropyridin-2-yl Derivatives -
pp. 389-407
Pavel Pihera, Hana Dvořáková and Jiří Svoboda* Diels-Alder Reactions of Vinyl Derivatives of [1]Benzothieno[3,2-b]furan -
pp. 408-416
Mária Incze, Gábor Dörnyei, Mária Kajtár-Peredy and Csaba Szántay* Intramolecular Mannich Reaction of 2-Oxotryptamines with Acetone Yielding Spiro[indole-3,3'-pyrrolidin]-2-ones -
pp. 417-434
Věra Klimešová*, Martin Svoboda, Karel Waisser, Milan Pour and Jarmila Kaustová Synthesis and Antimicrobial Activity of New 4-(Benzylsulfanyl)pyridine Derivatives
* In paper with more than one author, the asterisk indicates the name of the author to whom correspondence should be addressed.
