@article{oai:fukuyama-u.repo.nii.ac.jp:00006377,
 journal = {福山大学薬学部研究年報, Annual report of the Faculty of Pharmacy & Pharmaceutical Sciences, Fukuyama University},
 month = {},
 note = {P(論文), The reaction of 2,3-lutidine N-oxide (I) with phenyl isocyanate (IIa) in dimethylformamide at 110℃ gave a 1:2 adduct (IIIa). Under reflux in ethanolic potassium hydroxide, IIIa readily lost a component of IIa and was converted to 5-methyl-6-N-phenylcarbamoylmethyl-3-pyridinol (IVa) in 95% yield. 2-Phenylpyricline N-oxides (V-VII) reacted with phenyl isocyanates (II) to afford 1:1 cycloadducts (IX-XI and XII-XIV). The reaction of 2-(p-nitrophenyl)pyridine N-oxide (VIII) with hIa directly afforded 2-anilino-6-(p-nitrophenyl)pyridine derivatives (XIVa and XVa).},
 pages = {26--31},
 title = {Reaction of Aromatic N-Oxides with Dipolarophiles : V. 1,3-Cycloaddition of 2-Substituted Pyridine N-Oxides with Phenyl Isocyanates},
 volume = {1},
 year = {1982}
}