- ISSN 0010-0765 printed
- ISSN 1212-6950 electronic
1976, Volume 41, Issue 2
-
pp. 325-336
L. Kubelková and J. Nováková Formation of hydroxyl groups and exchange with deuterium on NaHX and NaHY zeolites -
pp. 337-341
E. Žůrková, S. Darioti and J. Kálal Reaction of crosslinked copolymers based on styrene-methacrylaldehyde with diamines -
pp. 342-349
J. Nývlt Seeding and its effect on size of product crystals in a batch crystallizer -
pp. 350-359
M. Hronec and V. Veselý Effect of alkylamines, alkanolamines, diamines, and amino acids on the activity of cobalt bromide catalysts -
pp. 360-367
J. Schraml, J. Pola, H. Jancke, G. Engelhardt, M. Černý and V. Chvalovský Application of 29Si-NMR to analysis of silylated compounds. NMR spectra of (CH3)3Si-O-C derivatives -
pp. 368-373
J. Pola, L. Cvak and V. Chvalovský 1,1,3,3-Tetramethyl-1,3-disila-2,6-dioxacyclooctane and 1,1,3,3,9,9,11,11-octamethyl-1,3,9,11-tetrasila-2,6,10,14-tetraoxacyclohexadecane -
pp. 374-385
J. Pola, M. Jakoubková and V. Chvalovský A study of intermolecular interaction between silicon and functional group in (diethoxymethylsilyl)alkyl acetates -
pp. 386-390
J. Včelák, V. Chvalovský, M. G. Voronkov, V. B. Pukhnarevich and V. A. Pestunovich 19F-NMR spectra of (fluoroalkyl)-substituted silanes -
pp. 391-394
V. Chvalovský, J. Pola, V. B. Pukhnarevich, L. I. Kopylova, E. O. Tsetlina, V. A. Pestunovich, B. A. Trofimov and M. G. Voronkov The effect of the structure of silanes on selectivity of hydrosilylation of 1-hexine -
pp. 395-407
J. Málek and E. Zelená Kinetics of the glycolysis of aromatic carboxamides catalysed in solution by metal ions -
pp. 408-412
A. Košturiak and A. Perjéssy The infrared spectra of some substituted 3-phenyliminoxindole derivatives -
pp. 413-429
J. Smolíková, M. Tichý and K. Bláha Infrared spectroscopy of 4-azatricyclo[4,4,0,03,8]decan-5-one - A lactam with a non-planar cis-amide group -
pp. 430-432
V. Bekárek, J. Jirkovský, K. Pragerová and J. Socha Solvent effect on valence vibration of NH bond of acetanilides and phenylcarbamates -
pp. 433-442
V. Kadeřábek and K. Kalfus Inductive effect in series of nitraminomonocarboxylic and -dicarboxylic acids -
pp. 443-458
J. O. Jílek, I. Červená, Z. Kopicová, K. Šindelář, E. Svátek, J. Metyšová, A. Dlabač, J. Pomykáček and M. Protiva Potent neuroleptic agents: Some new amino alcohols of the 10-piperazinodibenzo[b,f]thiepin series and their derivatives -
pp. 459-464
Z. Kopicová, J. Němec and M. Protiva Potential ganglionic and neuromuscular blocking agents: 1-Aryl-4-methyl-4-substituted piperazinium iodides -
pp. 465-471
A. Pískala and F. Šorm Reaction of 3,5,6-trichloro-1,2,4-triazine with dimethylamine and methanolysis of 3,6-dichloro-5-dimethylamino-1,2,4-triazine -
pp. 472-478
V. Uchytilová, J. Hájková, P. Fiedler, Z. Györgydeák, J. Škoda and J. Gut Preparation of 3,5-dioxohexahydro-1,2,4-triazine-1-carboxylic acid (dihydro-6-azaorotic acid) derivatives -
pp. 479-488
K. Hejno and F. Šorm Cyclic analogues of insect juvenile hormone -
pp. 489-497
H. Keilová and V. Tomášek Isolation and some properties of cathepsin D inhibitor from potatoes -
pp. 498-506
O. Dračka Reactions of products of very rapid parallel irreversible follow-up reactions in the galvanostatic method with current reversal -
pp. 507-521
J. Balej, M. Čížek and M. Thumová Phase diagram of the conversion system 2 NH4+, 2 Na+, SO42-, S2O82--H2O at 20 °C -
pp. 522-525
V. Procházka and J. Šubrt Catalysts of the reaction of sodium with hydrogen producing sodium hydride with a large specific surface -
pp. 526-535
V. Peroutková and L. Beránek Rate-retarding effect of products on some pairs of reactions catalysed by Al2O3 and PdO and differences in their interactions with catalyst surface -
pp. 536-539
J. Nývlt and M. Broul Generalized design relations for continuous mixed crystallizer -
pp. 540-547
L. Kábrt and Z. Holzbecher Fluorimetric determination of beryllium with o-pyridinophenol -
pp. 548-561
M. Studničková, J. Smola and P. Přecechtěl Ternary chelates with 2,2'-dipyridyl and 1,10-phenanthroline -
pp. 562-568
O. Exner, V. Jehlička and A. Dondoni Stereochemistry of the (2+2) cycloaddition between aryl isothiocyanates and dicyclohexylcarbodiimide: A dipole moment study -
pp. 569-580
O. Exner and K. Kalfus Concerning the transmission of substituent effects across the benzene nucleus -
pp. 581-589
J. Pola and V. Chvalovský Dual behaviour of (CH3)3SiCH2 and (CH3)3GeCH2 groups in oxygen-containing α-carbofunctional compounds -
pp. 590-597
J. Kaválek, V. Macháček, A. Lyčka and V. Štěrba Kinetics of reaction of 2,4-dinitrochlorobenzene with methyl malonate, cyanoacetate and acetoacetate -
pp. 598-603
M. Ferles, O. Kocián, M. Lebl, J. Lövy, S. Rádl, A. Šilhánková and P. Štern Electrolytic reduction of quaternary salts of some alcohols of the pyridine series, of corresponding alkylpyridines and alkenylpyridines -
pp. 604-610
J. Urbanec, M. Strašák, M. Hrušovský and J. Vojtko Oxidation of methylpentenes by thallium(III) sulfate -
pp. 611-613
J. Urbanec, M. Strašák, J. Vojtko and M. Hrušovský Semiempirical relations between structure and reactivity for the oxidation of alkenes by thallium(III) sulfate in aqueous medium -
pp. 614-616
D. Végh, J. Kováč and B. Hasová Preparation of geometric isomers of 2-(2-bromovinyl)-5-nitrofuran -
pp. 617-622
V. Janout, M. Procházka and M. Paleček Reaction of 1,2-dihalides with thilates -
pp. 623-632
L. Fišnerová, B. Kakáč, E. Kraus and O. Němeček erythro- and threo-Isomers of 2,3,4-substituted butanoic acids -
pp. 633-646
M. Kuchař, B. Brůnová, V. Rejholec, Z. Roubal and O. Němeček Synthesis and fibrinolytic activity of β-arylaliphatic acids. Quantitative relationships between structure and biological activity -
pp. 647-665
A. Holý Preparation of substituted (±)-5t-hydroxymethyl-3t-aminocyclopentane-1r,2c-diol derivatives related to carbocyclic ribonucleoside analogues -
pp. 666-673
L. Morávek and B. Meloun Sequential analysis of fragment CB3(Cys) of human plasma albumin. N-Terminal sequence and tryptic peptides
* In paper with more than one author, the asterisk indicates the name of the author to whom correspondence should be addressed.