@article{821ecfe6056c43d59f7f15898ae22ce3,
title = "Regioselectivity of the intramolecular biaryl coupling reaction of 3-substituted phenyl 2-iodobenzoate using a palladium reagent",
abstract = "This study investigated the regioselectivity of the intramolecular biaryl coupling reaction of the phenyl benzoate derivative which possesses a methyl or methoxy group at the meta-position of the phenoxy moiety. The type of base and the presence/absence of the phosphine ligand influenced the product ratio. A transition state model and the regioselectivity of the reaction are discussed.",
author = "Kazuhiro Maeda and Takuya Matsukihira and Shumpei Saga and Yasuo Takeuchi and Takashi Harayama and Yoshikazu Horino and Hitoshi Abe",
note = "Funding Information: A part of this research was financially supported by the JSPS KAKENHI Grant. No. 22590003 to H. A. The authors thank the SC-NMR Laboratory of Okayama University for the NMR experiments. Funding Information: A part of this research was financially supported by the JSPS KAKENHI Gr Publisher Copyright: {\textcopyright} 2014 The Japan Institute of Heterocyclic Chemistry.",
year = "2014",
doi = "10.3987/COM-13-S(S)10",
language = "English",
volume = "88",
pages = "621--628",
journal = "Heterocycles",
issn = "0385-5414",
publisher = "Japan Institute of Heterocyclic Chemistry",
number = "1",
}