@article{oai:toyama.repo.nii.ac.jp:00015614,
 author = {Maeda, Kazuhiro and Matsukihira, Takuya and Saga, Shumpei and Takeuchi, Yasuo and Harayama, Takashi and Horino, Yoshikazu and Abe, Hitoshi},
 issue = {1},
 journal = {Heterocycles, Heterocycles},
 month = {},
 note = {application/pdf, This study investigated the regioselectivity of the intramolecular 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., Article, Heterocycles 88(1), 621-628.(2014)},
 pages = {621--628},
 title = {REGIOSELECTIVITY OF THE INTRAMOLECULAR BIARYL COUPLING REACTION OF 3-SUBSTITUTED PHENYL 2-IODOBENZOATE USING A PALLADIUM REAGENT},
 volume = {88},
 year = {2014}
}