@article{oai:nagoya.repo.nii.ac.jp:00027948,
 author = {Kitamura, Yuki and Murata, Yuki and Oguri, Ayaka and Matsumura, Mio and Kakusawa, Naoki and Naka, Hiroshi and Yasuike, Shuji},
 issue = {1},
 journal = {Asian Journal of Organic Chemistry},
 month = {Jan},
 note = {Regioselective C−H arylation using pentavalent organoantimony compounds as a new class of arylating reagents is described. The reaction of thiophenes with triarylantimony difluorides in the presence of 5 mol% of Pd(OAc)2 and 2 equiv. CuCl2 at 80 °C under aerobic conditions afforded the β‐arylated thiophene derivatives in moderate‐to‐high yields. The reaction is sensitive to the electronic nature of the triarylantimony difluorides – those bearing an electron‐donating group on the phenyl ring showed higher reactivity than those have an electron‐withdrawing group., ファイル公開：2020-01-01},
 pages = {138--143},
 title = {Pd‐Catalyzed β‐Selective C−H Arylation of Thiophenes with Triarylantimony Difluorides},
 volume = {8},
 year = {2019}
}