Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Taizo, Iwayama"'
Autor:
Hiroshi Ikeda, Yuichi Kitamoto, Tetsutaro Hattori, Taizo Iwayama, Kenkichi Sakamoto, Sotaro Miyano, Osamu Yamabe, Koichi Natori
Publikováno v:
Chirality. 27:479-486
Two analogs of blestriarene C (4,4'-dimethoxy-1,1'-biphenanthrene-2,2',7,7'-tetraol) bearing no 7,7'-dihydroxy (3) and 4,4'-dimethoxy groups were prepared. Unlike blestriarene C (1), compounds and , as well as 1,1'-biphenanthrene-2,2'-diol (5), do no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d35a3ef9b3bd82bf711d0c30cae860f6
https://doi.org/10.1002/chir.22447
https://doi.org/10.1002/chir.22447
Autor:
Koichi, Natori, Taizo, Iwayama, Osamu, Yamabe, Yuichi, Kitamoto, Hiroshi, Ikeda, Kenkichi, Sakamoto, Tetsutaro, Hattori, Sotaro, Miyano
Publikováno v:
Chirality. 27(8)
Two analogs of blestriarene C (4,4'-dimethoxy-1,1'-biphenanthrene-2,2',7,7'-tetraol) bearing no 7,7'-dihydroxy (3) and 4,4'-dimethoxy groups were prepared. Unlike blestriarene C (1), compounds and , as well as 1,1'-biphenanthrene-2,2'-diol (5), do no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4f4cfc71db9a2f4412f562c1b27f7f92
https://pubmed.ncbi.nlm.nih.gov/25944278
https://pubmed.ncbi.nlm.nih.gov/25944278
Publikováno v:
ChemInform. 40
Here, we report a synthesis of a differentially protected, open-chain C21-C40 fragment of azaspiracid-1, corresponding to the lower half EFGHI-ring domain. The synthesis features modular coupling of three advanced intermediates, aiming for diverted a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b47b46bd5a21438347d52130a4282548
https://doi.org/10.1002/chin.200928197
https://doi.org/10.1002/chin.200928197
Publikováno v:
Organic letters. 8(18)
Here, we report a synthesis of the lower half C21−C40 fragment of the shellfish toxin, azaspiracid-1. The C28−C40 fragment was synthesized by a coupling between the C28−C35 epoxide and the C36−C40 dithioacetal anion, followed by the HI-ring s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f76e2efd29ed7f4f38426421da149d53
https://pubmed.ncbi.nlm.nih.gov/16928044
https://pubmed.ncbi.nlm.nih.gov/16928044
Publikováno v:
HETEROCYCLES. 78:609
Here, we report a synthesis of a differentially protected, open-chain C21-C40 fragment of azaspiracid-1, corresponding to the lower half EFGHI-ring domain. The synthesis features modular coupling of three advanced intermediates, aiming for diverted a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::384d17527b67b053085159db25ca2c6d
https://doi.org/10.3987/com-08-11555
https://doi.org/10.3987/com-08-11555