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Results: 1-8 |
Results: 8
Spirobipyridopyrans and indolinospiropyridopyrans: Synthesis, x-ray crystal structure, separation of enantiomers, and barriers to thermal cleavage ofthe C(sp(3))-O bond
Authors: Loncar-Tomaskovic, L Pustet, N Mrvos-Sermek, D Nagl, A Mintas, M Mannschreck, A
Citation: L. Loncar-tomaskovic et al., Spirobipyridopyrans and indolinospiropyridopyrans: Synthesis, x-ray crystal structure, separation of enantiomers, and barriers to thermal cleavage ofthe C(sp(3))-O bond, CHIRALITY, 13(2), 2000, pp. 81-88
Synthesis and antitumor activities of novel pyrimidine derivatives of 2,3-O,O-dibenzyl-6-deoxy-L-ascorbic acid and 4,5-didehydro-5,6-dideoxy-L-ascorbic acid
Authors: Raic-Malic, S Svedruzic, D Gazivoda, T Marunovic, A Hergold-Brundic, A Nagl, A Balzarini, J De Clercq, E Mintas, M
Citation: S. Raic-malic et al., Synthesis and antitumor activities of novel pyrimidine derivatives of 2,3-O,O-dibenzyl-6-deoxy-L-ascorbic acid and 4,5-didehydro-5,6-dideoxy-L-ascorbic acid, J MED CHEM, 43(25), 2000, pp. 4806-4811
Chromatographic resolution, circular dichroism spectra, absolute configurations, and crystal structures of bridged biphenyls, containing sulfide, sulfoxide, and sulfone groups in the bridge
Authors: Loncar-Tomascovic, L Sarac-Arneri, R Hergold-Brundic, A Nagl, A Mintas, M Sandstrom, J
Citation: L. Loncar-tomascovic et al., Chromatographic resolution, circular dichroism spectra, absolute configurations, and crystal structures of bridged biphenyls, containing sulfide, sulfoxide, and sulfone groups in the bridge, HELV CHIM A, 83(2), 2000, pp. 479-494
Spirobinaphthopyrans: Synthesis, X-ray crystal structure, separation of enantiomers, and barriers to thermal racemization
Authors: Loncar-Tomaskovic, L Lorenz, K Hergold-Brundic, A Mrvos-Sermek, D Nagl, A Mintas, M Mannschreck, A
Citation: L. Loncar-tomaskovic et al., Spirobinaphthopyrans: Synthesis, X-ray crystal structure, separation of enantiomers, and barriers to thermal racemization, CHIRALITY, 11(5-6), 1999, pp. 363-372
Synthesis and biological evaluation of the novel purine and pyrimidine nucleoside analogues containing 2,3-epoxypropyl, 3-amino-2-hydroxypropyl or 2,3-epoxypropyl ether moieties
Authors: Raic-Malic, S Grdisa, M Pavelic, K Mintas, M
Citation: S. Raic-malic et al., Synthesis and biological evaluation of the novel purine and pyrimidine nucleoside analogues containing 2,3-epoxypropyl, 3-amino-2-hydroxypropyl or 2,3-epoxypropyl ether moieties, EUR J MED C, 34(5), 1999, pp. 405-413
NMR characterization of novel purine nucleoside analogues with 2,3-epoxypropyl or 3-amino-2-hydroxypropyl moiety
Authors: Raic-Malic, S Vikic-Topic, D Mintas, M
Citation: S. Raic-malic et al., NMR characterization of novel purine nucleoside analogues with 2,3-epoxypropyl or 3-amino-2-hydroxypropyl moiety, SPECT LETT, 32(4), 1999, pp. 649-660
Novel pyrimidine and purine derivatives of L-ascorbic acid: Synthesis and biological evaluation
Authors: Raic-Malic, S Hergold-Brundic, A Nagl, A Grdisa, M Pavelic, K De Clercq, E Mintas, M
Citation: S. Raic-malic et al., Novel pyrimidine and purine derivatives of L-ascorbic acid: Synthesis and biological evaluation, J MED CHEM, 42(14), 1999, pp. 2673-2678
HeI photoelectron spectra of o,o '-bridged biphenyls by 2-X-propylene (X =O, S, SO, NCH3) chains
Authors: Kovac, B Klasinc, L Vukosa, E Loncar-Tomaskovic, L Mintas, M
Citation: B. Kovac et al., HeI photoelectron spectra of o,o '-bridged biphenyls by 2-X-propylene (X =O, S, SO, NCH3) chains, CROAT CHEM, 72(1), 1999, pp. 43-54
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