@article{oai:soar-ir.repo.nii.ac.jp:00019896,
 author = {Shoji, Taku and Takagaki, Sho and Tanaka, Miwa and Araki, Takanori and Sugiyama, Shuhei and Sekiguchi, Ryuta and Ohta, Akira and Ito, Shunji and Okujima, Tetsuo},
 issue = {10},
 journal = {HETEROCYCLES},
 month = {Oct},
 note = {Tetraarylpyrroles with a 1-azulenyl substituent were prepared by the reaction of 1-azulenyl ketones, which have various aryl-substituents at their alpha-position, with benzoin in the presence of ammonium acetate as a nitrogen source of the pyrrole ring. Optical property of the tetraarylpyrroles obtained by the reaction was clarified by UV/Vis spectroscopy and/or time-dependent density functional theory (TD-DFT) calculations., Article, HETEROCYCLES. 94(10):1870-1883 (2017)},
 pages = {1870--1883},
 title = {Synthesis of Azulene-Substituted Tetraarylpyrroles by Reaction of 1-Azulenyl Ketones with Benzoin and Ammonium Acetate},
 volume = {94},
 year = {2017}
}