Rchr
J-GLOBAL ID：200901018515036444
Update date: May. 15, 2020
Watanabe Nobuko
ワタナベ ノブコ | Watanabe Nobuko
Affiliation and department：
Kanagawa University Faculty of Science, Department of Materials Science
About Kanagawa University Faculty of Science, Department of Materials Science
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Detailed information
Research field (2)：
Bioorganic chemistry
, Structural/physical organic chemistry
Research theme for competitive and other funds (4)：
多置換芳香族化合物の簡便合成法の開発
発光基質としての1,2-ジオキセタンの設計と合成
Convenient synthesis of polysubstituted aromatic compounds
Design and synthesis of 1,2-dioxetanes as a chemiluminescent substrate
MISC (28)：
N Watanabe, Y Nagashima, T Yamazaki, M Matsumoto. Fluoride-induced chemiluminescent decomposition of dioxetanes bearing a siloxyaryl moiety to produce an alkyl aryl ketone as an emitter. TETRAHEDRON. 2003. 59. 26. 4811-4819
N Watanabe, Y Nagashima, T Yamazaki, M Matsumoto. Fluoride-induced chemiluminescent decomposition of dioxetanes bearing a siloxyaryl moiety to produce an alkyl aryl ketone as an emitter. TETRAHEDRON. 2003. 59. 26. 4811-4819
MATSUMOTO M, MIZUNO T, WATANABE N. Fluoride-induced chemiluminescent decomposition of 1,2-dioxetanes bearing a phenyl moiety substituted with a methyl having an electron-withdrawing group "jointly worked".
J. Chem. Soc. Chem. Commun.
. 2003. 4. 482-483
M Matsumoto, T Mizuno, N Watanabe. Fluoride-induced chemiluminescent decomposition of 1,2-dioxetanes bearing a phenyl moiety substituted with a methyl having an electron-withdrawing group. CHEMICAL COMMUNICATIONS. 2003. 4. 482-483
M Matsumoto, Y Ito, M Murakami, N Watanabe. Synthesis of 5-tert-butyl-1-(3-tert-butyldimethylsiloxy)phenyl-4,4-dimethyl-2,6,7-trioxabicyclo[3.2.0]heptanes and their fluoride-induced chemiluminescent decomposition: effect of a phenolic electron donor on the CIEEL decay rate in aprotic polar solvent. LUMINESCENCE. 2002. 17. 5. 305-312
ｍore...
Association Membership(s) (2)：
光化学協会
, 日本化学会
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