@article{oai:u-ryukyu.repo.nii.ac.jp:02006933,
 author = {外間, 宏三 and 与儀, 誠一 and Hokama, Kozo and Yogi Seiichi},
 issue = {15},
 journal = {琉球大学理工学部紀要. 理学編, Bulletin of Science & Engineering Division, University of Ryukyus. Mathematics & natural sciences},
 month = {Mar},
 note = {1,3,5-triaryl- 2-pyrazoline was irradiated with an ultraviolet light in ethanol under an oxygen atmosphere. The main products were 1.3, 5-triarylpyrazole (1.3, 5-triphenyl-2-pyrazoline to give 1.3, 5-tripheny - pyrazole in a 65% yield. 1,5-diphenyl- 3-(p-methylphenyl)-2-pyrazolioe to give1.5- diphenyl-3-(p-methylphenyl) - pyrazole in a 82% yield, 1,5-diphenyl - 3- (p-methoxyphenyl)-2 -pyrazoiine to give 1,5 – dipheny l- 3 - (p- methoxyphenyl)- pyrazole in a 65% yield and l,5- diphenyl - 3 - (p-chlorophenyl) -2-pyrazoline to give 1,5- diphenyl-3-(p- chlorophenyl )- pyrazole in a 56% yield). The reaction were followed by the determination of the disappearance of pyrazoline and that of the formation or pyrazole, Samo reactions of these compounds are described., 紀要論文},
 pages = {59--65},
 title = {1、3、5-トリアリル-2-ピラゾリンの光酸化反応},
 year = {1972}
}