Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Masayoshi Toyoda"'
Publikováno v:
Bulletin of the Chemical Society of Japan. 63:1316-1321
Methoxymethyl phenyl sulfoxide 1 undergoes acid-catalyzed hydrolysis to give S-phenyl benzenethiosulfinate 5, which is formed rapidly from a primary product, benzenesulfenic acid 3. Formation of 5 follows pseudo-first-order kinetics. Rate constants o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db5b85dd029400f8892901b36d6881db
https://doi.org/10.1246/bcsj.63.1316
https://doi.org/10.1246/bcsj.63.1316
Autor:
Takuo Morimoto, Ryosuke Sasaki, Hiroyuki Koike, Masaharu Nozawa, Shigeo Kawasaki, Masayoshi Toyoda, Ryuta Sonoda
Publikováno v:
Journal of Advanced Science. 14:99-100
In this paper, the antenna analysis simulator made by the object oriented programming was reported. This simulator based on a plug-in frame structure was composed by GUI, a FDTD solver and a Moment Method solver. These elements were combined in the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ed22e590876703d73c7b6809a0406c5
https://doi.org/10.2978/jsas.14.99
https://doi.org/10.2978/jsas.14.99
Publikováno v:
ChemInform. 21
Methoxymethyl phenyl sulfoxide 1 undergoes acid-catalyzed hydrolysis to give S-phenyl benzenethiosulfinate 5, which is formed rapidly from a primary product, benzenesulfenic acid 3. Formation of 5 follows pseudo-first-order kinetics. Rate constants o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b2598bf3a06f27696ca6465e30c11a0
https://doi.org/10.1002/chin.199039146
https://doi.org/10.1002/chin.199039146
Publikováno v:
Canadian Journal of Chemistry. 64:1116-1123
Hydrolyses of 2-ethylidene-(1b), 2-isopropylidene-(1c), and 2-benzylidene-1,3-dithiolane (1d) were kinetically investigated in aqueous solution. All the individual rate constants involved in this three-step reaction were evaluated. Initial carbon pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e010330302c1fb18b1ea7f80e61f5a36
https://doi.org/10.1139/v86-187
https://doi.org/10.1139/v86-187