@article{oai:nagoya.repo.nii.ac.jp:00024635,
 author = {Yamamoto, Yoshihiko and Nishimura, Kei-ichiro and Mori, Shota and Shibuya, Masatoshi},
 issue = {20},
 journal = {ANGEWANDTE CHEMIE-INTERNATIONAL EDITION},
 month = {May},
 note = {In the presence of a cationic Ru catalyst, 1,6-diynes bearing a terminal styryl moiety underwent [2+2+2] cyclization to produce dehydrobiphenylenes fused with a five-membered ring. Although the cycloadducts were unstable toward purification, their one-pot iodine-mediated ring expansion successfully afforded unprecedented bridged ketone products containing a benzo-fused bicyclo[3.2.1] framework.},
 pages = {5494--5497},
 title = {Assembly of a Benzo-Fused Bridged Ketone Scaffold from 1,5,10-Enediynes through One-Pot Ruthenium-Catalyzed Cyclization/Iodine-Mediated Oxidative Ring Expansion},
 volume = {56},
 year = {2017}
}