Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Tetsuya Sekiba"'
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 22:567-573
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d00e022832af464ca3153ad376d5750
https://doi.org/10.5059/yukigoseikyokaishi.22.567
https://doi.org/10.5059/yukigoseikyokaishi.22.567
Autor:
Tetsuya Sekiba, Yutaka Kodama
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 21:788-793
Syntheses of the monosubstituent (chloroform-amidine compounds) and the disubstituents (guainidine compounds) were investigated by the reaction of primary amines and secondary amines with isocyanodichloro group (N: CCl2) of 2, 4-dichluro-6-isocyanodi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ec2cdea5886c8569b4cf5ca74f52a91
https://doi.org/10.5059/yukigoseikyokaishi.21.788
https://doi.org/10.5059/yukigoseikyokaishi.21.788
Autor:
Tetsuya Sekiba
Publikováno v:
Bulletin of the Chemical Society of Japan. 46:577-580
2,3-Dihydromaculosidine and 2,3-dihydropteleine were obtained from 2,4-dimethoxy- and 4-methoxy-aniline by condensation with diethyl β-benzyloxyethylmalonate, followed by methylation and subsequent cyclodebenzylation with polyphosphoric acid. The de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce107a131462b99c5e4fe209977136bc
https://doi.org/10.1246/bcsj.46.577
https://doi.org/10.1246/bcsj.46.577
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 22:749-754
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3a8b309e56f4b79f9fc201aa0a19264
https://doi.org/10.5059/yukigoseikyokaishi.22.749
https://doi.org/10.5059/yukigoseikyokaishi.22.749
Autor:
Tetsuya Sekiba
Publikováno v:
Chemischer Informationsdienst. 9
2,3-Dihydroheliparvifoline (Va) was obtained from 4-methoxy-3-benzyloxyaniline by condensation with diethyl (2-benzyloxyethyl)-malonate, and by subsequent methylation, debenzylation, and then cyclodehydration. Benzyl ether of Va was dehydrogenated an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c39be8abf20809749b9de762b6b1fe9a
https://doi.org/10.1002/chin.197815235
https://doi.org/10.1002/chin.197815235
Autor:
Tetsuya Sekiba
Publikováno v:
Chemischer Informationsdienst. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73b1b62c9eb7cf417d634e413528acff
https://doi.org/10.1002/chin.197505290
https://doi.org/10.1002/chin.197505290
Autor:
Tetsuya Sekiba
Publikováno v:
Chemischer Informationsdienst. 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::517f00a16bf03215e2bd7a01a636c98b
https://doi.org/10.1002/chin.197318480
https://doi.org/10.1002/chin.197318480
Autor:
Tetsuya Sekiba
Publikováno v:
Bulletin of the Chemical Society of Japan. 47:2895-2896
2,3-Dihydroacronycidine (VIa) was obtained from 2,3,5-trimethoxyaniline by condensation with diethyl β-benzyloxyethylmalonate, methylation, debenzylation, and then cyclodehydration. The dehydrogenation of Via gave acronycidine in relatively high yie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f66b3a1125b21462315fcf0494adebcd
https://doi.org/10.1246/bcsj.47.2895
https://doi.org/10.1246/bcsj.47.2895
Autor:
Tetsuya Sekiba
Publikováno v:
Bulletin of the Chemical Society of Japan. 51:325-326
2,3-Dihydroheliparvifoline (Va) was obtained from 4-methoxy-3-benzyloxyaniline by condensation with diethyl (2-benzyloxyethyl)-malonate, and by subsequent methylation, debenzylation, and then cyclodehydration. Benzyl ether of Va was dehydrogenated an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9362228d464f7d01306db8f187735995
https://doi.org/10.1246/bcsj.51.325
https://doi.org/10.1246/bcsj.51.325
Publikováno v:
Bulletin of the Chemical Society of Japan. 31:997-998
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e78dd53f3506e1809178b4f3ebe21dc3
https://doi.org/10.1246/bcsj.31.997
https://doi.org/10.1246/bcsj.31.997