Zobrazeno 1 - 10
of 58
pro vyhledávání: '"K K, Ogilvie"'
Autor:
K. K. Ogilvie, Youla S. Tsantrizos
Publikováno v:
ChemInform. 22
The antifungal antibiotic pisolithin B (p-hydroxymandelic acid, 2-(4′-hydroxyphenyl)-2-hydroxyethanoic acid, 1a) was shown to have the absolute (R) configuration. The stereochemistry was establishe...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9615980b830606925cff7c77e6aa3aa9
https://doi.org/10.1002/chin.199140253
https://doi.org/10.1002/chin.199140253
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f20d0fa4d9a17f75eb6502eef2c24ea0
https://doi.org/10.1002/chin.199313300
https://doi.org/10.1002/chin.199313300
Autor:
Youla S. Tsantrizos, K. K. Ogilvie
Publikováno v:
Canadian Journal of Chemistry. 69:772-778
The antifungal antibiotic pisolithin B (p-hydroxymandelic acid, 2-(4′-hydroxyphenyl)-2-hydroxyethanoic acid, 1a) was shown to have the absolute (R) configuration. The stereochemistry was established via comparison of its optical rotation to that of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::487216e040a3d239268873fb5ca70483
https://doi.org/10.1139/v91-115
https://doi.org/10.1139/v91-115
Publikováno v:
Canadian Journal of Microbiology. 37:258-264
Two antifungal compounds isolated from the liquid culture medium of Pisolithus arhizus were identified as p-hydroxybenzoylformic acid and (R)-(−)-p-hydroxymandelic acid and given the trivial names pisolithin A and pisolithin B, respectively. The ef
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3772e82a2431af2d7b37b0548022a55
https://doi.org/10.1139/m91-040
https://doi.org/10.1139/m91-040
Autor:
M J, Damha, K K, Ogilvie
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e65bef2170f20d5c44f6cf1e2752305d
https://pubmed.ncbi.nlm.nih.gov/8242149
https://pubmed.ncbi.nlm.nih.gov/8242149
Publikováno v:
Antimicrobial Agents and Chemotherapy. 22:55-61
A novel nucleoside analog, 9-[[2-hydroxy-1-(hydroxymethyl)ethoxy]methyl]-guanine (BIOLF-62), was found to have potent antiviral activity against herpes simplex virus types 1 and 2 at concentrations well below cytotoxic levels. For example, the Patton
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74544a7aa40b897ee92fcc1c6fedbb9c
https://doi.org/10.1128/aac.22.1.55
https://doi.org/10.1128/aac.22.1.55
Publikováno v:
Antimicrobial Agents and Chemotherapy. 22:1026-1030
9-[[2-Hydroxy-1-(hydroxymethyl)ethoxy]methyl]guanine (BIOLF-62) is highly synergistic with either phosphonoformate or phosphonoacetate when used in combination against herpes simplex virus types 1 and 2 in vitro. Acycloguanosine did not show signific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b937ecf2420edf7a5337a5a583360e4
https://doi.org/10.1128/aac.22.6.1026
https://doi.org/10.1128/aac.22.6.1026
Autor:
D. Iwacha, K. K. Ogilvie
Publikováno v:
Canadian Journal of Chemistry. 47:495-497
Uridine 2′,3′-carbonates are readily converted to 2,2′-anhydrouridines in hot dimethyl formamide with base catalysis. 3′,5′-Di-O-trityluridine is converted to 3′,5′-di-O-trityl-2,2′-anyhdro-1-β-D-arabinofuranosyluracil with diphenyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7aee709b2b03658795ff38aac79eba9
https://doi.org/10.1139/v69-072
https://doi.org/10.1139/v69-072
Autor:
D. Iwacha, K. K. Ogilvie
Publikováno v:
Canadian Journal of Chemistry. 48:862-864
The synthesis of a nucleotide derivative (3) which can lead directly to O2,2′-anhydro- and arabino- analogues of 1-β-D-ribofuranosyluracil nucleotides is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e17b82b8c0223092acdd24c45d230414
https://doi.org/10.1139/v70-139
https://doi.org/10.1139/v70-139
Publikováno v:
Chemischer Informationsdienst. 16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fff512b0e968f99fba058c61efaefbc
https://doi.org/10.1002/chin.198537319
https://doi.org/10.1002/chin.198537319