@article{oai:tsukuba.repo.nii.ac.jp:00054853,
 author = {藤田, 健志 and FUJITA, Takeshi and 市川, 淳士 and ICHIKAWA, Junji and Kubo, Teruhiko},
 issue = {3},
 journal = {Chemistry Letters},
 month = {Mar},
 note = {The [4 + 2] cycloaddition of styrenes with arynes was achieved via 1:1 cross-coupling by a nickel catalyst. This protocol applies to a variety of styrenes and arynes generated in situ from o-(trimethylsilyl)aryl triflates to afford 9,10-dihydrophenanthrenes involving substituted aromatic rings. By using this method, a naturally occurring stilbenoid is easily synthesized.},
 pages = {264--266},
 title = {Nickel-catalyzed [4 + 2] Cycloaddition of Styrenes with Arynes via 1:1 Cross-coupling : Synthesis of 9,10-Dihydrophenanthrenes},
 volume = {49},
 year = {2020},
 yomi = {フジタ, タケシ and イチカワ, ジュンジ}
}