Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mikako, Ono"'
Autor:
Mikako, Ono, Kimiko, Kitagawa
Publikováno v:
共立女子大学・共立女子短期大学総合文化研究所紀要 = Bulletin of center for interdisciplinary studies of science and culture Kyoritsu Women's University & Kyoritsu Women's Junior College. 24:53-61
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::83cbfe3539e39aa8ebd1cfe53284227e
http://id.nii.ac.jp/1087/00003174/
http://id.nii.ac.jp/1087/00003174/
Autor:
Akemi Umeyama, Mayo Tani, Kazuko Yoshikawa, Shinya Bando, Shigenobu Arihara, Shinji Imoto, Mikako Ono
Publikováno v:
CHEMICAL & PHARMACEUTICAL BULLETIN. 52:354-358
Three new diterpenes, sugikurojins A-C (1-3) were isolated from the black heartwood of Cryptomeria japonica. The structure of sugikurojin A was deduced to be 19-hydroxy-6,7-dehydroferruginol on the basis of extensive NMR experiments. Sugikurojin B wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca1240f7bf785fb0c0e5d66cdca6fcba
https://doi.org/10.1248/cpb.52.354
https://doi.org/10.1248/cpb.52.354
Autor:
Mikako Ono, Shinya Bando, Mayo Tani, Kazuko Yoshikawa, Shigenobu Arihara, Shinji Imoto, Akemi Umeyama
Publikováno v:
ChemInform. 35
Three new diterpenes, sugikurojins A-C (1-3) were isolated from the black heartwood of Cryptomeria japonica. The structure of sugikurojin A was deduced to be 19-hydroxy-6,7-dehydroferruginol on the basis of extensive NMR experiments. Sugikurojin B wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43ee39678c547ad2a3491a3b106d01ff
https://doi.org/10.1002/chin.200434201
https://doi.org/10.1002/chin.200434201
Publikováno v:
Chemicalpharmaceutical bulletin. 52(4)
Three new sesquiterpenes, (4S)-2,6,10-bisaboratrien-4-ol-1-one (1), 1,8-epoxy-1(6),2,4,7,10-bisaborapenta-en-4-ol (2), and 1-methoxy-4-cadinene (3) have been isolated from the black heartwood of Cryptomeria japonica. Compounds 1 and 2 were designated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b0f57265747618e5f327ea0cb9bce83
https://pubmed.ncbi.nlm.nih.gov/15056967
https://pubmed.ncbi.nlm.nih.gov/15056967
Autor:
Akiko, Aoki, Eri, Hagiwara, Shigeru, Ono, Atsuhisa, Ueda, Takashi, Tsuji, Yuko, Inoue, Mikako, Ono, Shohei, Nagaoka, Yoshiaki, Ishigatsubo
Publikováno v:
Arerugi = [Allergy]. 51(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f5f05ded0ebc8cf7f8bb4e1427ec8820
https://pubmed.ncbi.nlm.nih.gov/12014028
https://pubmed.ncbi.nlm.nih.gov/12014028
Publikováno v:
HETEROCYCLES. 62:491
The novel synthesis of 6- or 7-aromatic substituted 2H-isoquinolin-1-ones, by two different routes is described. In the first route, 7-substituted derivatives were prepared by regioselective iodination at the 7-position of 6,8-dihydroxy-4-ethoxycarbo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b82ad588efe684cf39b2dcf39435bbf
https://doi.org/10.3987/com-03-s(p)43
https://doi.org/10.3987/com-03-s(p)43