@article{oai:nagasaki-u.repo.nii.ac.jp:00020360,
 author = {Libendi, Samuel S. and Demizu, Yosuke and Matsumura, Yoshihiro and Onomura, Osamu},
 issue = {18},
 journal = {Tetrahedron},
 month = {Apr},
 note = {N-Protecting groups of α-substituted cyclic amines strongly affected the regioselectivity in electrochemical methoxylation of these compounds. Namely, N-acyl derivatives were transformed into α′-methoxylated compounds, while N-cyano derivatives changed into α-methoxylated derivatives. Furthermore, Lewis acid catalyzed nucleophilic substitution of the α-methoxylated compounds protected with cyano group afforded α,α-disubstituted cyclic amines., Tetrahedron, 64(18), pp.3935-3942; 2008},
 pages = {3935--3942},
 title = {High regioselectivity in electrochemical α-methoxylation of N-protected cyclic amines},
 volume = {64},
 year = {2008}
}