@article{oai:fukuyama-u.repo.nii.ac.jp:00008733,
 author = {阿部, 匠 and 仲村, 修平 and 柳田, 玲子 and 町支, 臣成 and 日比野, 俐 and 石倉, 稔},
 issue = {32},
 journal = {福山大学薬学部研究年報, Annual report of the Faculty of Pharmacy & Pharmaceutical Sciences, Fukuyama University},
 month = {Dec},
 note = {A one-pot approach to 3,3'-bisindolylmethane derivatives from nitrobenzene derivatives through the Bartoli indole synthesis was developed, in which the acid used to quench the reaction markedly affected its outcome. Quenching the reaction with concd HCl produced 3,3'-bisindolylmethane in contrast to the formation of 7-substituted indole by quenching with NH4Cl., A one-pot approach to 3,3'-bisindolylmethane derivatives from nitrobenzene derivatives through the Bartoli indole synthesis was developed, in which the acid used to quench the reaction markedly affected its outcome. Quenching the reaction with concd HCl produced 3,3'-bisindolylmethane in contrast to the formation of 7-substituted indole by quenching with NH4Cl.},
 pages = {20--20},
 title = {Bartoli インドール合成による3,3'-ビスインドリルメタンのワンポット構築(発表論文抄録(2013))},
 year = {2014}
}