@article{oai:kanagawa-u.repo.nii.ac.jp:00006907,
 author = {Matsumoto, Masakatsu and 松本, 正勝 and Ohashi, Mamoru and 大橋, 守 and Watanabe, Nobuko and 渡辺, 信子 and Fujimori, Ken and 藤森, 憲},
 journal = {Science Journal of Kanagawa University},
 month = {May},
 note = {Bicyclic dioxetane bearing a (3-cyanoethenyl) phenyl group was found to be triggered by the Michael addition of a malonate anion with an accompanying emission of red light. 3-Adamantylidene-4-methoxy-1,2-dioxetanes bearing a 4-(3-hydroxy)phenyl substituted with a podand-type group, namely, 1,4,7-trioxaoctyl, 1,4,7,10-tetraoxaundecyl, or 1,4,7,10,13 -pentaoxa- tetradecyl were synthesized and their base-induced chemiluminescent decomposition was examined in an aqueous system. Optically active dioxetanes bearing a naphthylnaphthol moiety were also synthesized. They exhibited chemilumines" cence in molecular recognition.},
 pages = {83--85},
 title = {Mechanistic Aspects of Bioluminescence and Chemiluminescence(By a grant Reserch Institute for Integrated Science, Kanagawa University)},
 volume = {16},
 year = {2005}
}