Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Kazuo Irie"'
Autor:
Kazuo, Irie
Publikováno v:
共立女子大学文芸学部紀要 = The Kyoritsu journal of arts and letters. 62:1-21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::cfede660f41a561f18128a692b677b72
http://id.nii.ac.jp/1087/00003100/
http://id.nii.ac.jp/1087/00003100/
Autor:
Maiko Nakamura, Kazuo Irie
Publikováno v:
The Proceedings of the Annual Convention of the Japanese Psychological Association. 84-075
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2d9add36e6906661b8e532b322ea770
https://doi.org/10.4992/pacjpa.84.0_pp-075
https://doi.org/10.4992/pacjpa.84.0_pp-075
Autor:
Kazuo, Irie
Publikováno v:
共立女子大学文芸学部紀要 = Studies in arts and letters. 58:1-36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::4f6b2be82193c1944ee8fb4bb03fd912
http://id.nii.ac.jp/1087/00002435/
http://id.nii.ac.jp/1087/00002435/
Publikováno v:
Annals of the New York Academy of Sciences. 588:387-388
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ccea638798956991d3b5e288f66a52f
https://doi.org/10.1111/j.1749-6632.1990.tb13241.x
https://doi.org/10.1111/j.1749-6632.1990.tb13241.x
Autor:
Kazuo Irie, Ken-ichi Watanabe
Publikováno v:
Bulletin of the Chemical Society of Japan. 53:1366-1371
Aldol condensations of aldehydes with ketones catalyzed by the first-row transition metal(II) complexes have been widely studied. Complexes of Co(II), Ni(II), Cu(II), and Zn(II) acetates with 2,2′-bipyridine were effective catalysts to afford cross
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e44f56f972c6a44f4df63934d9ea0e4d
https://doi.org/10.1246/bcsj.53.1366
https://doi.org/10.1246/bcsj.53.1366
Autor:
Kazuo Irie, Ken-ichi Watanabe
Publikováno v:
Bulletin of the Chemical Society of Japan. 54:1195-1198
The rate of the condensation of benzaldehyde with excess acetophenone catalyzed by Co(II) acetate-2,2′-bipyridine complex was obtained by GLC analysis. The rate increased in proportion as the amount of the complex catalyst. 2,2′-Bipyridine ligand
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f8ce2a72146df767b9bbec90196161d
https://doi.org/10.1246/bcsj.54.1195
https://doi.org/10.1246/bcsj.54.1195
Publikováno v:
Chemischer Informationsdienst. 11
In the presence of nickel(II) or cobalt(II)acetate-2,2′-bipyridine complexes, α,β-unsaturated ketones, methyl acrylate, and acrylonitrile were found to react with nitromethane, malononitrile, and aniline at room temperature under neutral conditio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62e2cb02042ddf47427ccbd3f916485e
https://doi.org/10.1002/chin.198043070
https://doi.org/10.1002/chin.198043070
Autor:
Ken-ichi Watanabe, Kazuo Irie
Publikováno v:
Chemischer Informationsdienst. 11
Aldol condensations of aldehydes with ketones catalyzed by the first-row transition metal(II) complexes have been widely studied. Complexes of Co(II), Ni(II), Cu(II), and Zn(II) acetates with 2,2′-bipyridine were effective catalysts to afford cross
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3600d4cdbb77cd5ddcdc7dd7396d837e
https://doi.org/10.1002/chin.198033107
https://doi.org/10.1002/chin.198033107
Publikováno v:
Chemischer Informationsdienst. 14
Michael-addition reactions have been found to proceed in the presence of the Ni(OAc)2 or Co(OAc)2-2,2′-bipyridine complex in DMF under neutral conditions at room temperature without any by-product. The reactions of chalcone and its derivatives with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0e794fab8fb0c000e30705e6c25b1cd
https://doi.org/10.1002/chin.198303120
https://doi.org/10.1002/chin.198303120
Autor:
Kazuo Irie, Ken-ichi Watanabe
Publikováno v:
Chemischer Informationsdienst. 9
The aldol condensation of benzaldehyde with 2-butanone, catalyzed by 2,2′-bipyridine or ethylenediamine copper(II) complexes, afforded the regioselective reaction product at the C1-position of 2-butanone. The yield and regioselectivity of the aldol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fabbfbb4eff66689da62f685cf8474c9
https://doi.org/10.1002/chin.197843097
https://doi.org/10.1002/chin.197843097