2006

Kraus T., Buděšínský M., Závada J.:
Synthesis of per-6-guanidinylated cyclodextrins.
Tetrahedron Letters 47 (5): 679-681, 2006.

Kraus T., Buděšínský M., Cvačka J., Sauvage J.-P.:
Copper(I)-directed formation of a cyclic pseudorotaxane tetramer and its trimeric homologue.
Angewandte Chemie - International Edition 45 (2): 258-261, 2006.

Buděšínský M., Poláková J., Hamerníková M., Císařová I., Trnka T., Černý M.:
1,6-Anhydro-1-thio-β-D-glucopyranose (thiolevoglucosan) and the corresponding sulfoxides and sulfone.
Collection of Czechoslovak Chemical Communications 71 (3): 311-336, 2006.

Herrmann P., Kotora M., Buděšínský M., Šaman D., Císařová I.:
Synthesis of (±)-3-methoxyestra-1,3,5(10)-trienes by the repetitive use of Negishi reagent.
Organic Letters 8 (7): 1315-1318, 2006.

Jiráček J., Collinsová M., Rosenberg I., Buděšínský M., Netušilová H., Garrow T.A.:
S-alkylated homocysteine derivatives: New inhibitors of human betaine-homocysteine S-methyltransferase.
Journal of Medicinal Chemistry 49 (13): 3982-3989, 2006.

Lindsey K.L., Buděšínský M., Kohout L., van Staden J.:
Antibacterial activity of maytenonic acid isolated from the root-bark of Maytenus senegalensis.
South African Journal of Botany 72 (3): 473-477, 2006.

Džoganová M., Černý M., Buděšínský M., Dračínský M., Trnka T.:
Epoxide migration and pseudo-epoxide migration of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses. Synthesis of some deoxy halo derivatives of 1,6-anhydro-β-D-hexopyranoses.
Collection of Czechoslovak Chemical Communications 71 (10): 1497-1515, 2006.

Točík Z., Barvík I., Buděšínský M., Rosenberg I.:
Novel isosteric, isopolar phosphonate analogs of oligonucleotides: preparation and properties.
Biopolymers 83 (4): 400-413, 2006.

Králíková Š., Buděšínský M., Tomečková I., Rosenberg I.:
Oxidative cleavage of ribofuranose 5-(α-hydroxyphosphonates): a route to erythrofuranose-based nucleoside phosphonic acids.
Tetrahedron 62 (41): 9742-9750, 2006.

Harmatha J., Buděšínský M., Vokáč K., Dinan L., Lafont R.:
Dimeric ecdysteroid analogues and their interaction with the Drosophila ecdysteroid receptor.
Collection of Czechoslovak Chemical Communications 71 (8): 1229-1238, 2006.

Králíková Š., Buděšínský M., Masojídková M., Rosenberg I.:
Nucleoside 5'-C-phosphonates: reactivity of the alpha-hydroxyphosphonate moiety.
Tetrahedron 62 (20): 4917-4932, 2006.

Dračínský M., Richtr V., Křeček V., Sejbal J., Klinot J, Buděšínský M.:
Preparation and conformational study of 19β,28-epoxy-18α-olean-5-ene derivatives.
Collection of Czechoslovak Chemical Communications 71 (3): 387-410, 2006.

Dračínský M., Hybelbauerová S., Sejbal J., Buděšínský M.:
Preparation and conformational study of B-ring substituted lupane derivatives.
Collection of Czechoslovak Chemical Communications 71 (8): 1131-1160, 2006.

Poljaková J., Dračínský M., Frei E., Hudeček J., Stiborová M.:
The effect of pH on peroxidase-mediated oxidation and DNA-adduct formation by ellipticine.
Collection of Czechoslovak Chemical Communications 71 (8): 1169-1185, 2006.

Hřebabecký H., Masojídková M., Dračínský M., Holý A.:
Synthesis of novel conformationally locked carbocyclic nucleosides derived from 3-(hydroxymethyl)bicyclo[2.2.1]heptane-2,5-diol.
Collection of Czechoslovak Chemical Communications 71 (6): 871-888, 2006.

Česnek M., Masojídková M., Holý A., Šolínová V., Koval D., Kašička V.:
Synthesis and properties of 2-guanidinopurines.
Collection of Czechoslovak Chemical Communications 71 (9): 1303-1319, 2006.

Nencka R., Votruba I., Hřebabecký H., Tloušťová E., Horská K., Masojídková M., Holý A.:
Design and synthesis of novel 5,6-disubstituted uracil derivatives as potent inhibitors of thymidine phosphorylase.
Bioorganic & Medicinal Chemistry Letters 16 (5): 1335-1337, 2006.

Šála M., Hřebabecký H., Masojídková M., Holý A.:
Synthesis of novel rcemic conformationally locked carbocyclic nucleosides derived from 7-substituted bicyclo[2.2.1]hept-5-en-2,2-dimethanols.
Collection of Czechoslovak Chemical Communications 71 (5): 635-649, 2006.

Krečmerová M., Masojídková M., Holý A.:
Preparation of C-5 Substituted Cidofovir derivatives.
Collection of Czechoslovak Chemical Communications 71 (4): 579-594, 2006.

Páv O., Protivínská E., Pressová M., Collinsová M., Jiráček J., Snášel J., Masojídková M., Buděšínský M., Rosenberg I.:
Activation of murine RNase L by isopolar 2 '-phosphonate analogues of 2 ',5 ' oligoadenylates.
Journal of Medicinal Chemistry 49 (13): 3955-3962, 2006.

Hořejší K., Andrei G., De Clercq E., Snoeck R., Pohl R., Holý A.:
Tricyclic etheno analogs of PMEG and PMEDAP: Synthesis and biological activity.
Biorganic & Medicinal Chemistry 14 (23): 8057-8065, 2006.

Montes V. A., Pohl R., Shinar J., Anzenbacher, P. Jr.:
Effective manipulation of the electronic effects and its influence on the emission of 5-substituted tris(8-quinolinolate)aluminium (III) complexes.
Chemistry – A European Journal 12 (17): 4523-4535, 2006.

Čapek P., Vrábel M., Hasník Z., Pohl R., Hocek M.:
Aqueous-phase Suzuki-Miyaura cross-coupling reactions of free halopurine bases.
Synthesis (20): 3515-3526, 2006.

Čapek P., Pohl R., Hocek M.:
Cross-coupling reactions of unprotected halopurine bases, nucleosides, nucleotides and nucleoside triphosphates with 4-boronophenylalanine in water. Synthesis of (purin-8-yl)- and (purin-6-yl)phenylalanines.
Organic & Biomolecular Chemistry 4 (11): 2278-2284, 2006.

Čerňa I., Pohl R., Votruba I., Klepetářová B., Hocek M.:
Direct C-H arylation of purines: Development of methodology and its use in regioselective synthesis of 2,6,8-trisubstituted purines.
Organic Letters 8 (23): 5389-5392, 2006.

Kapitán J., Baumruk V., Kopecký V. Jr., Pohl R., Bouř P.:
Proline zwitterion dynamics in solution, glass, and crystalline state.
Journal of the American Chemical Society 128 (41): 13451-13462, 2006.

Kočalka P., Pohl R., Rejman D., Rosenberg I.:
Synthesis of racemic and enantiomeric 3-pyrrolidinyl derivatives of nucleobases.
Tetrahedron 62 (24): 5763–5774, 2006.

Kuchař M., Pohl R., Votruba I., Hocek M.:
Synthesis of purines bearing functionalized C-substituents by the conjugate addition of nucleophiles to 6-vinylpurines and 6-ethynylpurines.
European Journal of Organic Chemistry (22): 5083-5098, 2006.

Novák P., Pohl R., Kotora M., Hocek M.:
Synthesis of C-aryldeoxyribosides by [2+2+2]-cyclotrimerization catalyzed by Rh, Ni, Co and Ru complexes.
Organic Letters 8 (10): 2051-2054, 2006.

Hořejší K., Pohl R., Holý A.:
Tricyclic purine analogs derived from 2-amino-6-chloropurine and 2,6-diaminopurine and their methylated quaternary salts.
Collection of Czechoslovak Chemical Communications 71 (1): 77-90, 2006.

Pomeisl K., Votruba I., Holý A., Pohl R.:
Syntheses of base and side-chain modified pyrimidine 1-[2-(phosphonomethoxy)propyl] derivatives as potent inhibitors of thymidine phosphorylase (PD-ECGF) from SD-lymphoma.
Collection of Czechoslovak Chemical Communications 71 (4): 595-624, 2006.

Šilhár P., Pohl P., Votruba I., Klepetářová B., Hocek M.:
Synthesis of 6-amino-, 6-methyl- and 6-aryl-2-(hydroxymethyl)purine bases and nucleosides.
Collection of Czechoslovak Chemical Communications 71 (6): 788-803, 2006.

Hocek M., Šilhár P., Pohl R.:
Cytostatic and antiviral 6-arylpurine ribonucleosides VIII. Synthesis and evaluation of 6-substituted purine 3'-deoxyribonucleosides.
Collection of Czechoslovak Chemical Communications 71 (10): 1484-1496, 2006.

Rybáčková M., Bělohradský M., Holý P., Pohl R., Závada J.:
Versatile synthesis of triptycene di- and tetracarboxylic acids.
Synthesis (12): 2039-2042, 2006.

Šilhár P., Pohl R., Votruba I., Hocek M.:
Synthesis and cytostatic activity of novel 6-(difluoromethyl)purine bases and nucleosides.
Synthesis (11): 1848-1852, 2006.

Turek P., Novák P., Pohl R., Hocek M., Kotora M.:
Preparation of highly substituted 6-arylpurine ribonucleosides by Ni-catalyzed cyclotrimerization. Scope of the reaction.
The Journal of Organic Chemistry 71 (23): 8978-8981, 2006.

Urban M., Pohl R., Klepetářová B., Hocek M.:
New modular and efficient approach to 6-substituted pyridin-2-yl C-nucleosides.
The Journal of Organic Chemistry 71 (19): 7322-7328, 2006.

Vrbovská S., Holý A., Pohl R., Masojídková M.:
Bifunctional acyclic nucleoside phosphonates. 1. Symmetrical 1,3-bis[phosphonomethoxy)propan-2-yl] derivatives of purines and pyrimidines.
Collection of Czechoslovak Chemical Communications 71 (4): 543-566, 2006.

Veselý I., Rohlenová A., Džoganová M., Trnka T., Tišlerová I., Šaman D., Ledvina M.:
Preparation of ethyl 2-azido-2-deoxy-1-thio-β-D-mannopyranosides, and their rearrangement to 2-S-ethyl-2-thio-β-D-mannopyranosylamines.
Synthesis (4): 699-705, 2006.

Starý I., Stará I.G., Alexandrová Z., Sehnal P., Teplý F., Šaman D., Rulíšek L.:
Helicity control in the synthesis of helicenes and related compounds.
Pure and Applied Chemistry 78 (2): 495-499, 2006.

Alexandrová Z., Sehnal P., Stará I.G., Starý I., Šaman D., Urquhart S.G., Otero E.:
Modified synthesis of heptahelicene and its resolution into single enantiomers.
Collection of Czechoslovak Chemical Communications 71 (8): 1256-1264, 2006.

Šaman D., Wimmerová M., Wimmer Z.:
Synthesis and structure assignment of 2-(4-methoxybenzyl)cyclohexyl β-D-galactopyranoside stereoisomers.
Collection of Czechoslovak Chemical Communications 71 (8): 1186-1198, 2006.

Šaman D., Cvačka J., Svatoš A., Bouman E.A.P., Kalinová B.:
Structural identification of an anthrasteroid hydrocarbon from the sheep tick Ixodes ricinus.
Journal of Natural Products 69 (8): 1203-1205, 2006.

Šaman D., Kratina P., Moravcová J., Wimmerová M., Wimmer Z.:
Synthesis and structure of 2-(4-methoxybenzyl)cyclohexyl β-D-glucopyranoside enantiomers.
Collection of Czechoslovak Chemical Communications 71 (10): 1470-1483, 2006.

Xanthakis E., Zarevúcka M., Šaman D., Wimmerová M., Kolisi F.N., Wimmer Z.:
Application of ionic liquids in enzymic resolution by hydrolysis of cycloalkyl acetates.
Tetrahedron: Assymetry 17 (21): 2987-2992, 2006.

Kapitán J., Baumruk V., Hulačová H., Maloň P.:
Raman optical activity of the hinge peptide.
Vibrational Spectroscopy 42 (1): 88-92, 2006.

Niederhafner P., Šafařík M., Šebestík J., Gut V., Maloň P., Hlaváček J.:
Synthesis of protected peptides from the human IgG1 hinge region on PEG support using disulfide bond synthons and alkaline or enzymatic detachment.
Tetrahedron Letters 47 (6): 1023-1025, 2006.