Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Izumi Takano"'
Autor:
Tariq Shehzad, Tsuyoshi Tokunaga, Nobuhiro Nagasawa, Junichi Yoneda, Lin Shinsei, Shimpei Uraguchi, Izumi Takano, Hiroyuki Hattori, Kazutoshi Okuno, Hiroko Suzuki, Toru Fujiwara, Kenji Sakurai, Nobuhiro Tsutsumi, Masashi Itoh, Akio Watanabe, Hiroki Rai, Kana Tsuboi, Tomoko Saito, Shoji Morita, Yusuke Ito, Hiromori Akagi, Katsura Suzuki, Hidekazu Takahashi, Rumiko Itoh, Namiko Satoh-Nagasawa, Keiko Asari
Publikováno v:
Crop Science. 57:22-31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51cb0d275a769d1c93b09a05e8505f58
https://doi.org/10.2135/cropsci2016.01.0069
https://doi.org/10.2135/cropsci2016.01.0069
Autor:
Kana Tsuboi, Shehzad, Tariq, Junichi Yoneda, Shimpei Uraguchi, Yusuke Ito, Lin Shinsei, Shoji Morita, Hiroki Rai, Nobuhiro Nagasawa, Keiko Asari, Hiroko Suzuki, Rumiko Itoh, Tomoko Saito, Katsura Suzuki, Izumi Takano, Hidekazu Takahashi, Kenji Sakurai, Akio Watanabe, Hiromori Akagi, Tsuyoshi Tokunaga
Publikováno v:
Crop Science; Jan/Feb2017, Vol. 57 Issue 1, p22-31, 10p, 5 Charts, 6 Graphs
Publikováno v:
Journal of Colloid and Interface Science. 132:523-531
The ζ-potential of synthetic chrysotile asbestos in aqueous alkali halide MX (M = Li, Na, K, Cs; X = F, Cl, Br, I) solutions was measured by a microelectrophoretic method. The ζ-potential of chrysotile in water was a minimum at pH 6.3 and its isoel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe3875dda430e57457d7c1604968e1ea
https://doi.org/10.1016/0021-9797(89)90266-x
https://doi.org/10.1016/0021-9797(89)90266-x
Publikováno v:
Agricultural and Biological Chemistry. 53:1413-1415
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5891fe18e7377ef1652102915f5f2d7d
https://doi.org/10.1271/bbb1961.53.1413
https://doi.org/10.1271/bbb1961.53.1413
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb8bdbb4bdcf5e3aa6e260d4f9766437
https://doi.org/10.1002/chin.197120213
https://doi.org/10.1002/chin.197120213
Publikováno v:
J. Chem. Soc., Chem. Commun.. :989-990
The reaction of tributyltin enolates with α-halogeno ketones gave substituted furans which were not derived from the normal cross-coupling products, 1,4-diketones, but were formed instead through addition of the tin enolate to the α-halogeno ketone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8322ecbd752de6cc5d2b995ec40dbbf4
https://doi.org/10.1039/c39830000989
https://doi.org/10.1039/c39830000989
Publikováno v:
Bulletin of the Chemical Society of Japan. 44:567-567
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e1f0e93df52f4ffdf830f43482beeac
https://doi.org/10.1246/bcsj.44.567
https://doi.org/10.1246/bcsj.44.567