Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Jože Kobe"'
Publikováno v:
Synthesis. 2004:2026-2034
Reaction of N 2 -acetyl-9- and/or -7-benzylated guanines 8 and 12 with selected alkylating agents in l-methyl-2-pyrrolidone at 120 °C yielded the guaninium salts 9 and 13. The salts were consequently transformed by phase transfer hydrogenation into
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::076f86eb6f69c1aacdbd7358b9320341
https://doi.org/10.1055/s-2004-829174
https://doi.org/10.1055/s-2004-829174
Publikováno v:
International Journal of Mass Spectrometry. 230:141-150
Relative stabilities (ΔGc) of ammonium-bound monomers and dimers of anomeric β- d -pentofuranosyl 1α- and 1β-azide derivates are determinate using the kinetic method by measuring relative rates of competitive collision-induced dissociations of di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a045ee561dba7f38af0ad99dedf4fe49
https://doi.org/10.1016/j.ijms.2003.08.014
https://doi.org/10.1016/j.ijms.2003.08.014
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 59:o221-o224
The two title ethoxycarbonylmethoxy derivatives of calix[4]arene, namely diethyl 2,4-dihydroxycalix[4]arene-1,3-diyldi(oxyacetate), C36H36O8, (I), and tetraethyl calix[4]arene-1,2,3,4-tetrayltetra(oxyacetate), C44H48O1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::219724d350da05aa1aea4206dcb12537
https://doi.org/10.1107/s0108270103005298
https://doi.org/10.1107/s0108270103005298
Autor:
Andrzej Surdykowski, Edward Szłyk, Jerzy Sitkowski, Iwona Łakomska, Jože Kobe, Tadeusz Głowiak
Publikováno v:
Polyhedron. 21:2001-2007
A platinum(II) complex with 1-β- d -ribofuranosyl-1,2,4-triazole-3-carboxamide is obtained and characterised spectroscopically with 1H, 13C, 15N, 195Pt NMR and IR. Significant 15N NMR coordination shifts (−92.7 and +18.4 ppm) were observed, respec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23a82ff892584f93ac8ed46c381d8300
https://doi.org/10.1016/s0277-5387(02)01103-8
https://doi.org/10.1016/s0277-5387(02)01103-8
Publikováno v:
Rapid Communications in Mass Spectrometry. 15:551-562
Electron impact (EI), fast atom bombardment (FAB) and ammonia chemical ionization [CI(NH3)] mass spectrometry were applied with the aim of differentiating between the anomeric 1α- and 1β-azidopentofuranosyl derivatives. Calculated ammonium affiniti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6d407e7c46e30f86ec81dfaf20ebfd5
https://doi.org/10.1002/rcm.267
https://doi.org/10.1002/rcm.267
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :1433-1438
A variable temperature-dependent 1H NMR conformational analysis of 3JHH coupling constants and NOE enhancements of a series of 8-aza-3-deaza modified guanine nucleosides 2 and 4–8 has been performed in DMSO-d6 and the results compared to those for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::185f699106de5381428a59a36972b06f
https://doi.org/10.1039/b009401n
https://doi.org/10.1039/b009401n
Autor:
Jože Kobe, Anton Stimac
Publikováno v:
Carbohydrate Research. 324:149-160
The stereoselectivity of the 1,2-trans directed, Lewis acid-catalysed azidation of peracylated furanoses was found to depend on the reactivity of the azide donor (azide nucleophilicity) and the configuration at the anomeric centre relative to the nei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43c8b54a0cfd73d433ae7eb7fd242033
https://doi.org/10.1016/s0008-6215(99)00293-1
https://doi.org/10.1016/s0008-6215(99)00293-1
Publikováno v:
Synlett. 1999:1069-1073
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3dcce612240e39dc9d69a4bde067abf9
https://doi.org/10.1055/s-1999-2755
https://doi.org/10.1055/s-1999-2755
Autor:
Jože Kobe, Barbara Mohar
Publikováno v:
Nucleosides and Nucleotides. 18:443-456
Multi-step transformation of enantiomerically pure synthons, (1S,2S,3R,4R)-(4-hydroxymethyl-2,3-isopropylidenedioxy-l-cyclopentyl) methyl butyrate {(-)-5} and(1R,5R,6R,7S)-6,7-(isopropylidenedioxy)-3-oxabicyclo[3.2.1]octane-2-one {(+)-11} into carba-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f5fe3a133106edce82a851cff1f0658
https://doi.org/10.1080/15257779908043088
https://doi.org/10.1080/15257779908043088
Publikováno v:
Journal of the American Chemical Society. 120:2508-2513
A variable temperature 600 MHz 1H NMR conformational analysis of 3JHH coupling constants in pyrazolo[4,3-c]pyridine carbaribo-C-nucleoside 1 in D2O has shown that the carbocyclic nucleoside analogu...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3150a601f309cc7b433b748d5c03ba30
https://doi.org/10.1021/ja972433g
https://doi.org/10.1021/ja972433g