Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Kimio Takahashi"'
Autor:
Eric Hayot, Kimio Takahashi
Publikováno v:
Comparative Literature Studies. 47:263-265
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1e6de0972495928a3315cc474c35228
https://doi.org/10.5325/complitstudies.47.3.0263
https://doi.org/10.5325/complitstudies.47.3.0263
Autor:
Reiko Tachibana, Kimio Takahashi
Publikováno v:
Comparative Literature Studies. 45:1-3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1984577cbbc186bafca6643c9f9d32ca
https://doi.org/10.2307/25659628
https://doi.org/10.2307/25659628
Autor:
Hayot, Eric1 (AUTHOR), Kimio Takahashi1 (AUTHOR)
Publikováno v:
Comparative Literature Studies. 2010, Vol. 47 Issue 3, p263-265. 3p.
Autor:
Yasuyuki Kawanishi, Sanji Hagishita, Tadahiko Tsushima, Kimio Takahashi, Shoichi Ishihara, Michio Ishikawa, Yasunobu Ishihara
Publikováno v:
ChemInform. 28
In an attempt to improve the low oral absorbability of previously reported dual histamine H2 and gastrin receptor antagonists, compounds of a different type were synthesized and evaluated for biological activity. These new compounds bear a histamine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ba0ede2d5bc99404ec254d82868a5bd
https://doi.org/10.1002/chin.199731225
https://doi.org/10.1002/chin.199731225
Autor:
Hisato Kakushi, Kiyohisa Uchida, Nobuhiro Haga, Tatsuo Tsuri, Takeaki Matsui, Sanji Hagishita, Susumu Kamata, Kimio Takahashi, Atsushi Kurosawa, Hisao Hatakeyama
Publikováno v:
Chemical and Pharmaceutical Bulletin. 40:85-95
In a continuing effort to obtain more potent platelet activating factor (PAF) antagonists, we tried to synthesize a series of PAF-sulfonamide isosteres in which the substituent at the 2-position was modified to an acetoxy equivalent other than the me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f004b35818c5defa3100fa885312ec8
https://doi.org/10.1248/cpb.40.85
https://doi.org/10.1248/cpb.40.85
Autor:
Kimio, Takahashi
Publikováno v:
同志社商学 = Doshisha Shogaku (The Doshisha Business Review). 42(2):170-181
書評
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::401f8dcc199db1390cadf961270f5f03
http://id.nii.ac.jp/1707/00014390/
http://id.nii.ac.jp/1707/00014390/
Autor:
Tadahiko Tsushima, Sanji Hagishita, Yasuyuki Kawanishi, Michio Ishikawa, Kimio Takahashi, Shoichi Ishihara, Yasunobu Ishihara
Publikováno v:
Chemicalpharmaceutical bulletin. 45(1)
In an attempt to improve the low oral absorbability of previously reported dual histamine H2 and gastrin receptor antagonists, compounds of a different type were synthesized and evaluated for biological activity. These new compounds bear a histamine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2b6f461ec8235fa1a7d25fd1ff55209
https://pubmed.ncbi.nlm.nih.gov/9023973
https://pubmed.ncbi.nlm.nih.gov/9023973
Publikováno v:
Chemical and Pharmaceutical Bulletin. 26:1918-1922
Reaction of 2, 3-dihydro-7-methoxy-6-methyl-1H-pyrrolo [1, 2-a] indole-9-carboxaldehydes (2), (3), (4), (5), and (6) with thiolacetic acid in the presence of 6 N sulphuric acid at room temperature gave 9-diacetylthiomethyl-2, 3-dihydro-7-methoxy-6-me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc7589c66809459d2a9cea9b7ab7195e
https://doi.org/10.1248/cpb.26.1918
https://doi.org/10.1248/cpb.26.1918
Publikováno v:
Chemical and Pharmaceutical Bulletin. 26:3815-3819
Treatment of the 2, 3-dihydro-1H-pyrrolo [1, 2-a] indoles (1 and 7) with N-bromosuccinimide in protic solvents such as methanol and acetic acid yielded the brominated compounds (4 and 8). The reaction of the pyrrolo [1, 2-a] indole-5, 8-diones (9-13)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::852ac5ca50e5913c959d3596144ef054
https://doi.org/10.1248/cpb.26.3815
https://doi.org/10.1248/cpb.26.3815
Publikováno v:
Synthetic Communications. 18:37-43
An improved synthesis of the Lukes-Ŝorm dilactam 3 and conversion into several 5-substituted pyrrolidine-2-ones are described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4c32df5d2c7c6eeb8c642b3b21df989
https://doi.org/10.1080/00397918808057817
https://doi.org/10.1080/00397918808057817