@article{oai:nagoya.repo.nii.ac.jp:00024752,
 author = {Kitamura, Yuki and Matsumura, Mio and Murata, Yuki and Yamada, Mizuki and Kakusawa, Naoki and Tanaka, Motohiro and Okabe, Hiroyuki and Naka, Hiroshi and Obata, Tohru and Yasuike, Shuji},
 journal = {Journal of Fluorine Chemistry},
 month = {Jul},
 note = {Triarylantimony difluorides were synthesized in moderate to excellent yields by oxidative fluorination of triarylstibanes with nitrosyl tetrafluoroborate (NOBF4) under aerobic conditions. This reaction is the first example of fluorination of trivalent organoantimony compounds using NOBF4 as a fluorinating agent. The triarylantimony difluorides exhibited good anti-proliferation activity against tumor cell lines. In particular, the IC50 of p-Tol3SbF2 (2c) was the lowest in each cell lines.},
 pages = {1--6},
 title = {A versatile synthesis of triarylantimony difluorides by fluorination of triarylstibanes with nitrosyl tetrafluoroborate and their antitumor activity},
 volume = {199},
 year = {2017}
}