Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Seigoro Hayashi"'
Publikováno v:
Chemical and Pharmaceutical Bulletin. 23:580-585
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecf68856a50561b6918e3308b40491f9
https://doi.org/10.1248/cpb.23.580
https://doi.org/10.1248/cpb.23.580
Publikováno v:
Chemical and Pharmaceutical Bulletin. 24:1708-1713
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e90e47b848ae61fdc8128e28f32ef1b
https://doi.org/10.1248/cpb.24.1708
https://doi.org/10.1248/cpb.24.1708
Publikováno v:
Chemical and Pharmaceutical Bulletin. 20:2024-2028
The reactions of diaryl disulfide with N-chlorosuccinimide, N-chloroacetamide and N-chlorosaccharine were attempted. When diaryl disulfide was allowed to react with N-chlorosuccinimide in the presence of pyridine, N-arylsulfensuccinimide was obtained
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc2517ae22f363347453177225c61423
https://doi.org/10.1248/cpb.20.2024
https://doi.org/10.1248/cpb.20.2024
Publikováno v:
Chemical and Pharmaceutical Bulletin. 19:2247-2251
The reactions of sodium ethoxycarbonylmethylthiosulfate and sodium phenacylthiosulfate with amine was examined and found to proceed through the intermediate formation of bisethoxycarbonylmethyldisulfide and phenacyldisulfide at the first step to give
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46e57775473c7468e26740fbc01c1135
https://doi.org/10.1248/cpb.19.2247
https://doi.org/10.1248/cpb.19.2247
Publikováno v:
Chemical and Pharmaceutical Bulletin. 20:15-20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f162003827f83966a4a0bb8974667602
https://doi.org/10.1248/cpb.20.15
https://doi.org/10.1248/cpb.20.15
Publikováno v:
Chemical and Pharmaceutical Bulletin. 22:2875-2882
The reactions of arylbiguanides with isatin and with 1-methylisatin gave 2-oxo-3-arylbiguanidylidene-indoles and 4-amino-6-arylamino-2-(1'-methyl-2'-oxo-3'-indolidene)-1, 2-dihydro-s-triazines, respectively. Analogously, N-amidino-O-alkylisoureas rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3606bb2b31b16d04cc42fe63cc04b364
https://doi.org/10.1248/cpb.22.2875
https://doi.org/10.1248/cpb.22.2875
Publikováno v:
Chemical and Pharmaceutical Bulletin. 22:262-266
Arylthiation of the nucleophilic β-carbon atom of 1-morpholino-1-cyclohexene with arensulfensuccinimides and arensulfenamides was successfully carried out. Moreover, benzylthiosulfenylation of morpholine and thiophenol with benzylthiosulfenphthalimi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a3ca96948770f7486046c00169bd191
https://doi.org/10.1248/cpb.22.262
https://doi.org/10.1248/cpb.22.262
Publikováno v:
Endocrinologia Japonica. 13:223-233
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::259170e0d62ef2d66a791bae4c10fa32
https://doi.org/10.1507/endocrj1954.13.223
https://doi.org/10.1507/endocrj1954.13.223
Publikováno v:
Chemical and Pharmaceutical Bulletin. 21:811-816
The reactions of sodium 2-phenylcarbamoylethylthiosulfate, sodium 2-cyclohexylcarbamoylethylthiosulfate and sodium 2-benzoylethylthiosulfate with aqueous alkylamines were attempted and found to give the corresponding N-β-carbonylethyl-N-alkylamines
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b965a27141b5e3dbcecac19e90264e84
https://doi.org/10.1248/cpb.21.811
https://doi.org/10.1248/cpb.21.811
Publikováno v:
Chemical and Pharmaceutical Bulletin. 20:521-525
Heating of 1-substituted biguanide with benzil in ethanol was found to give 2-substituted guanidilidene-5, 5-diphenylhydantoin, which was easily converted into 1, 1-diphenyl-1-substituted biguanidoacetic acid by hydrolysis with hydrochloric acid. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1dae997b74f91869d73178dd008ca9d
https://doi.org/10.1248/cpb.20.521
https://doi.org/10.1248/cpb.20.521