Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Hiromi Oyama"'
Autor:
Hiromi, OYAMA, Ryoji, BABA, Reiko, WADA, Yukinori, TAGAWA, Yoko, ARASHI, Tomomi, SHIMAMOTO, Sachiko, YOSHISATO, Rieko, OBA
Publikováno v:
言語資源活用ワークショップ発表論文集 = Proceedings of Language Resources Workshop. 2:233-238
会議名: 言語資源活用ワークショップ2017, 開催地: 国立国語研究所, 会期: 2017年9月5日-6日, 主催: 国立国語研究所 コーパス開発センター
言語には様々な異種が存在する。方言（ここで
言語には様々な異種が存在する。方言（ここで
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::ff0e8ada9e66c49c7db52bb014c75c80
http://id.nii.ac.jp/1328/00001524/
http://id.nii.ac.jp/1328/00001524/
Publikováno v:
Journal of Natural Language Processing. 23:195-225
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc7e6cb644295156e7863450715fe9de
https://doi.org/10.5715/jnlp.23.195
https://doi.org/10.5715/jnlp.23.195
Publikováno v:
Organic letters. 18(15)
[7]Helicene-like compounds with a fluorene unit were successfully synthesized using a platinum-catalyzed double cyclization reaction. Crystal structures and photophysical properties of these compounds were also studied. In particular, they were found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::badea1ec35a66b4b4584c9890aa1fe03
https://pubmed.ncbi.nlm.nih.gov/27400646
https://pubmed.ncbi.nlm.nih.gov/27400646
Publikováno v:
Angewandte Chemie. 124:719-723
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62757ccd951c1640272de2509bbd4289
https://doi.org/10.1002/ange.201106157
https://doi.org/10.1002/ange.201106157
Publikováno v:
Tetrahedron Letters. 50:3411-3413
Ring-opening reaction of tetrahydrofuran takes place on penta(methyl)- and penta( n -butylphenyl)[60]fullerenes in the presence of chlorotrimethylsilane giving penta(organo)fullerene hydroxybutyl derivatives, C 60 R 5 (C 4 H 8 OH) (R = Me, n BuC 6 H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e12ec575ec5cbe9e64f8b8e933d443f1
https://doi.org/10.1016/j.tetlet.2009.02.155
https://doi.org/10.1016/j.tetlet.2009.02.155
Autor:
Koji Nakano, Kyoko Nozaki, Kazuyuki Nobusawa, Masanobu Naito, Takunori Harada, Hiromi Oyama, Reiko Kuroda
Publikováno v:
Organic letters. 15(9)
A facile synthetic route to dimethylsila[7]helicene by using a Lewis acid catalyzed double-cyclization reaction for construction of the twisted two phenanthrene moieties is described. Sila[7]helicene exhibited a high fluorescence quantum yield and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d6afb8f7724758502b2b0f8cf349a1c
https://pubmed.ncbi.nlm.nih.gov/23587064
https://pubmed.ncbi.nlm.nih.gov/23587064
Autor:
Yutaka Matsuo, Akinori Saeki, Shu Seki, Hiromi Oyama, Hideyuki Tanaka, Eiichi Nakamura, Iwao Soga, Toshihiro Okamoto
Publikováno v:
Chemistry, an Asian journal. 8(1)
The efficient nucleophilic addition of aryl Grignard reagents (aryl=4-MeOC(6)H(4), 4-Me(2)NC(6)H(4), Ph, 4-CF(3)C(6)H(4), and thienyl) to C(60) in the presence of DMSO produced 1,2-arylhydro[60]fullerenes after acid treatment. The reactions of the an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cb8a9836a91352b23f733ce4a29a9b0
https://pubmed.ncbi.nlm.nih.gov/23023947
https://pubmed.ncbi.nlm.nih.gov/23023947
Publikováno v:
Organic Letters; Aug2016, Vol. 18 Issue 15, p3654-3657, 4p
Publikováno v:
Agricultural and Biological Chemistry. 45:1327-1334
Useful cryophilic killer strains of Saccharomyces cerevisiae were bred by back-crossing KL-88, which is a wild killer sake yeast, with a repetitive parent WL-7 and is one of the best cryophilic wine yeasts. The hybrids maybe aid in producing good win
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30585dd229b556aadefea0a6b86ec93c
https://doi.org/10.1271/bbb1961.45.1327
https://doi.org/10.1271/bbb1961.45.1327
Publikováno v:
Agricultural and Biological Chemistry. 42:2407-2409
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e6a42e3130dbf8b05ac297e0cb900f0
https://doi.org/10.1271/bbb1961.42.2407
https://doi.org/10.1271/bbb1961.42.2407