@article{oai:nagasaki-u.repo.nii.ac.jp:00018276,
 author = {Onomura, Osamu and Moriyama, Atsushi and Fukae, Kazuhiro and Yamamoto, Yutaka and Maki, Toshihide and Matsumura, Yoshihiro and Demizu, Yosuke},
 issue = {47},
 journal = {Tetrahedron Letters},
 month = {Nov},
 note = {Oxidative carbon?carbon bond cleavage of N-alkoxycarbonylated cyclic amines was accomplished by NaNO2 in TFA to afford ω-amino carboxylic acid in high yield. Optically active 3-hydroxypiperidine derivatives and 3-pipecolinate were converted to enantiomerically pure (R)-4-amino-3-hydroxybutanoic acid (GABOB) and (S)-2-pyrrolidone-4-carboxylate, respectively., Tetrahedron Letters, 49(47), pp.6728-6731; 2008},
 pages = {6728--6731},
 title = {Oxidative C?C bond cleavage of N-alkoxycarbonylated cyclic amines by sodium nitrite in trifluoroacetic acid},
 volume = {49},
 year = {2008}
}