@article{oai:kanazawa-u.repo.nii.ac.jp:00014861,
 author = {Matsuo, Jun-ichi and Okano, Masahiko and Takeuchi, Kosuke and Tanaka, Hiroyuki and Ishibashi, Hiroyuki},
 issue = {16},
 journal = {Tetrahedron Asymmetry},
 month = {Aug},
 note = {Enantiomerically pure N-carbobenzyloxy-N′-phthaloyl-cis-1,2-cyclohexanediamine was synthesized by the asymmetric reduction of a β-enamino ester formed from benzyl 2-oxocyclohexanecarboxylate and (R)-phenylethylamine, followed by hydrogenolysis, phthaloylation, and the Curtius rearrangement. © 2007., 金沢大学大学院自然科学研究科生理活性物質科学, 金沢大学薬学部},
 pages = {1906--1910},
 title = {A practical synthesis of enantiopure N-carbobenzyloxy-N′-phthaloyl-cis-1,2-cyclohexanediamine by asymmetric reductive amination and the Curtius rearrangement},
 volume = {18},
 year = {2007}
}