Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Mimosamycin"'
Autor:
Surattana Amnuoypol, Sunibhond Pummangura, Chieko Tanaka, Akinori Kubo, Khanit Suwanborirux, Naoki Saito, Yu-ichi Koizumi
Publikováno v:
Tetrahedron. 60:3873-3881
The transformation of renieramycin M ( 1m ) into renieramycin J ( 1j ) and jorumycin ( 2 ) is presented along with the results of antiproliferative assay data. The chemical stability and the oxidative degradation of 2 and renieramycin E ( 1e ) to gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e11d39a27f6ea1848e2ae05e49e1d1e7
https://doi.org/10.1016/j.tet.2004.02.071
https://doi.org/10.1016/j.tet.2004.02.071
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d07395651a0d594f9138222a8d3e446
https://doi.org/10.1002/chin.199446267
https://doi.org/10.1002/chin.199446267
Autor:
Bart Kesteleyn, Norbert De Kimpe
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::387621037264cb59d62b1213d5d40906
https://doi.org/10.1002/chin.200023232
https://doi.org/10.1002/chin.200023232
Autor:
Bradley S. Davidson
Publikováno v:
Tetrahedron Letters. 33:3721-3724
A new cytotoxic alkaloid, renieramycin G ( 8 ), was isolated, along with previously reported metabolites mimosamycin ( 1 ), renierol ( 2 ), and N -formyl-1,2-dihydrorenierone ( 3 ), from the Fijian sponge Xestospongia caycedoi . The structure of reni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5554b920127ed025102eac292a2dec52
https://doi.org/10.1016/s0040-4039(00)91997-x
https://doi.org/10.1016/s0040-4039(00)91997-x
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Chemicalpharmaceutical bulletin. 52(2)
6-Hydroxy-7-methoxyisoquinolinemethanol (15) and mimosamycin (1) were recently isolated from a marine sponge, Haliclona sp. The former was prepared in ten steps from vanillin (22) in 26% overall yield using an isopropyl for phenol protection.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86edf7c88e259783751b576c0744c0e1
https://pubmed.ncbi.nlm.nih.gov/14758020
https://pubmed.ncbi.nlm.nih.gov/14758020
Autor:
Akinori Kubo, Shinsuke Nakahara
Publikováno v:
HETEROCYCLES. 63:1849
The one-pot synthesis of mimosamycin utilizing the Polonovski reaction and a five-step synthesis of 5,8-dihydroxy-4,7-dimethoxy-2,6-dimethylisoquinolinium iodide (7) from known compound (8) are described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d69612745e6b100605d5e284e7b452c2
https://doi.org/10.3987/com-04-10126
https://doi.org/10.3987/com-04-10126
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Dee Ann Casteel, Kathlyn A. Parker
Publikováno v:
The Journal of Organic Chemistry. 53:2847-2850
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5efae0a4504fbbd0c2bea0fc8bab3a8a
https://doi.org/10.1021/jo00247a038
https://doi.org/10.1021/jo00247a038
Autor:
Alexander McKillop, Stephen P. Brown
Publikováno v:
Synthetic Communications. 17:657-667
The marine antibiotic mimosamycin, and a number of analogues, have been prepared in two steps by cycloaddition of a 1,4-benzoquinone or naphthoquinone with 2-aza-bis(1,3-t-butyldimethylsilyloxy)-1,3-buta-diene, hydrolytic work-up of the adduct, and p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e28a7dfd71f3fb4d3023c753f00afa9
https://doi.org/10.1080/00397918708075739
https://doi.org/10.1080/00397918708075739