Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Kikoh Obi"'
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 10:1451-1454
A series of novel nikkomycin analogue inhibitors of the chitin synthase of fungal cell wall was synthesized and evaluated for their inhibitory activities. Among them, the compound having a phenanthrene group at the terminal amino acid was found to po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3e55ec9a85d2d56295efed707060eae
https://doi.org/10.1016/s0960-894x(00)00256-0
https://doi.org/10.1016/s0960-894x(00)00256-0
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 5:2777-2782
Synthesis and biological properties of a novel class of cephalosporins with a 2-[5-(3-hydroxy-4-pyridon-6-yl)1,3,4-oxadiazol-2-yl]thioethyl group at C-7 position are described. Among them, the compounds having a pyridiniumthiomethyl group at C-3 posi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e681d81e2bb33de1e11e9952f7ba0c96
https://doi.org/10.1016/0960-894x(95)00485-c
https://doi.org/10.1016/0960-894x(95)00485-c
Publikováno v:
ChemInform. 27
Synthesis and biological properties of a novel class of cephalosporins with a 2-[5-(3-hydroxy-4-pyridon-6-yl)1,3,4-oxadiazol-2-yl]thioethyl group at C-7 position are described. Among them, the compounds having a pyridiniumthiomethyl group at C-3 posi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f81f2ec2b2d1a1f930a3f990ddc6a415
https://doi.org/10.1002/chin.199614287
https://doi.org/10.1002/chin.199614287
Publikováno v:
Chemical and Pharmaceutical Bulletin. 38:917-924
Various structural types of monobactams bearing an (R)-1-hydroxyethyl and an (S)-1-carbamoyloxyethyl group at the C 3,4 -positions, respectively, could be synthesized from (3S,4S)-4-[(S)-1-benzyloxyethyl]-3-[(R)-1-hydroxyethyl]-2-azetidinone. These s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed1334ef21fb8ee51c52c68407b04e54
https://doi.org/10.1248/cpb.38.917
https://doi.org/10.1248/cpb.38.917
Publikováno v:
ChemInform. 31
A series of novel nikkomycin analogue inhibitors of the chitin synthase of fungal cell wall was synthesized and evaluated for their inhibitory activities. Among them, the compound having a phenanthrene group at the terminal amino acid was found to po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d196491dda90bfcb94159cec800cea89
https://doi.org/10.1002/chin.200041182
https://doi.org/10.1002/chin.200041182
Publikováno v:
Nucleic acids symposium series. (42)
A series of novel nikkomycin analogs, which inhibited chitin synthase, the fungal cell wall biosynthesis enzyme, has been synthesized and evaluated their inhibitory activities.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e475c74506be48e7ce8df4863a905e8
https://pubmed.ncbi.nlm.nih.gov/10780355
https://pubmed.ncbi.nlm.nih.gov/10780355
Publikováno v:
The Journal of antibiotics. 48(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd71748c6e7124656778c74b28a01184
https://pubmed.ncbi.nlm.nih.gov/7730166
https://pubmed.ncbi.nlm.nih.gov/7730166
Publikováno v:
The Journal of antibiotics. 48(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94a865980f68085bfbeaa1c1e0778877
https://pubmed.ncbi.nlm.nih.gov/7730165
https://pubmed.ncbi.nlm.nih.gov/7730165
Publikováno v:
Tetrahedron Letters. 28:87-90
Lithiation of 2′,3′,5′-tris- O -( tert -butyldimethylsilyl)uridine with sec -BuLi/TMEDA occurs at the C-5 position with a high regioselectivity and subsequent reactions of the resulting C-5 lithiated species with a variety of electrophiles prov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06f633d96afd63964fe908ce374031ef
https://doi.org/10.1016/s0040-4039(00)95656-9
https://doi.org/10.1016/s0040-4039(00)95656-9
Publikováno v:
Tetrahedron. 42:4187-4195
phenylthio group at the C-6 position of uridine serves as the protecting group during lithiation at the C-5 position with lithium 2,2,6,6-tetramethylpiperidide. Reactions of the resulting C-5 lithiated species with various types of electrophiles furn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::457b39eb637cf4bec31ce63fe8c7d3ef
https://doi.org/10.1016/s0040-4020(01)87642-0
https://doi.org/10.1016/s0040-4020(01)87642-0