Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Kazuo Kariyone"'
Publikováno v:
Tetrahedron Letters. 15:3991-3994
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84c66638265215312fba6c437b0df2a9
https://doi.org/10.1016/s0040-4039(01)92065-9
https://doi.org/10.1016/s0040-4039(01)92065-9
Publikováno v:
Journal of the agricultural chemical society of Japan. 50:495-499
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ddcb5794b9debb6e16d03ad5b781690
https://doi.org/10.1271/nogeikagaku1924.50.10_495
https://doi.org/10.1271/nogeikagaku1924.50.10_495
Autor:
Torizo Takahashi, Kazuo Kariyone
Publikováno v:
Chemical and Pharmaceutical Bulletin. 8:1106-1109
Hydrogenation of 2 (1H)-pyridones was carried out in methanol over Raney nickel at 120 atm. and 200∼240°and gave 2-piperidone derivatives. When the reduction temperature was raised to 280°, hydrogenation of carbonyl group took place, followed by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78b8c6d57f32d9a2914c9b77ca265ca5
https://doi.org/10.1248/cpb.8.1106
https://doi.org/10.1248/cpb.8.1106
Publikováno v:
YAKUGAKU ZASSHI. 77:182-186
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ae7ab5f13031668eb2310af4486d946
https://doi.org/10.1248/yakushi1947.77.2_182
https://doi.org/10.1248/yakushi1947.77.2_182
Autor:
Kiyotsugu Yamamoto, Kazuo Kariyone
Publikováno v:
YAKUGAKU ZASSHI. 75:1222-1225
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be30f702da0477e0dee346808d66d314
https://doi.org/10.1248/yakushi1947.75.10_1222
https://doi.org/10.1248/yakushi1947.75.10_1222
Autor:
Kazuo Kariyone, Torizo Takahashi
Publikováno v:
YAKUGAKU ZASSHI. 79:711-716
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26c2c9a3ff80fe74f1df72a25fdc2e04
https://doi.org/10.1248/yakushi1947.79.6_711
https://doi.org/10.1248/yakushi1947.79.6_711
Autor:
Kazuo Kariyone
Publikováno v:
YAKUGAKU ZASSHI. 83:398-401
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c7bc22530677be514db6a884ac30c2b
https://doi.org/10.1248/yakushi1947.83.4_398
https://doi.org/10.1248/yakushi1947.83.4_398
Autor:
Suminori Umio, Kunihiko Tanaka, Minoru Nishida, Teiji Kishimoto, Hitoshi Nakamura, Kazuo Kariyone
Publikováno v:
Chemical and Pharmaceutical Bulletin. 18:1414-1425
A number of de-chloro and de-nitro derivatives of pyrrolnitrin and the isomers as to the positions of the substituents were prepared and their antimicrobial activities were evaluated. Among the homologues having a nitro group, pyrrolnitrin has shown
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::869901b8f7580d7fb0a76cd5c20ec5ac
https://doi.org/10.1248/cpb.18.1414
https://doi.org/10.1248/cpb.18.1414
Publikováno v:
Chemical and Pharmaceutical Bulletin. 17:605-610
Preparation of 2, 5-dimethyl-3-arylpyrrole (IX) was accomplished by three different routes : at first alkyl 3-aryl-5-methyl-4-pyrrolecarboxylate (IV) was converted to IX by the series of reactions containing Mannich reaction, reduction and decarboxyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6b5535d2bb257925e4cd4b42ee83157
https://doi.org/10.1248/cpb.17.605
https://doi.org/10.1248/cpb.17.605
Publikováno v:
Chemical and Pharmaceutical Bulletin. 17:611-615
A new method of pyrrole ringclosure using an aminoacetal (V) was investigated. Condensation of 2-nitro-3-chlorophenylpyruvic acid (VIII) and 2-nitro-3-chlorophenylacetone (XVI) with V afforded 3-(2-nitro-3-chlorophenyl) pyrrole (XII) and 1-acetyl-2-m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32174a48dddea8d3812ae7a170e413f0
https://doi.org/10.1248/cpb.17.611
https://doi.org/10.1248/cpb.17.611