957060-26-3Relevant academic research and scientific papers
A practical synthesis of enantiopure N-carbobenzyloxy-N′-phthaloyl-cis-1,2-cyclohexanediamine by asymmetric reductive amination and the Curtius rearrangement
Matsuo, Jun-ichi,Okano, Masahiko,Takeuchi, Kosuke,Tanaka, Hiroyuki,Ishibashi, Hiroyuki
, p. 1906 - 1910 (2008/02/13)
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, phthaloyla
