@article{oai:soar-ir.repo.nii.ac.jp:00019894,
 author = {Shoji, Taku and Maruyama, Akifumi and Ito, Shunji and Okujima, Tetsuo and Yasunami, Masafumi and Higashi, Junya and Morita, Noboru},
 issue = {11},
 journal = {HETEROCYCLES},
 month = {Nov},
 note = {Preparation of 2-aryl- and 6-heteroarylazulenes 2-6 and 8-10 was established by the palladium-catalyzed cross-coupling reaction of the corresponding haloazulenes with lithium aryl- and heteroarylmagnesium ate complexes, which were readily prepared from the corresponding aryl and heteroaryl halides. The reaction of 2-6 and 8-10, except for 3 and 8, with pyridine in the presence of Tf2O, followed by treatment with KOH in MeOH afforded the corresponding 2-aryl- and 6-heteroary1-1,3-di(4-pyridyl)azulenes 11-16 in good yields., Article, HETEROCYCLES. 89(11):2588-2603 (2014)},
 pages = {2588--2603},
 title = {Synthesis of 2-Aryl- and 6-Heteroaryl-1,3-di(4-pyridyl)azulenes by Katritzky’s Pyridylation of 2-Aryl- and 6-Heteroarylazulenes},
 volume = {89},
 year = {2014}
}