Beilstein J. Org. Chem.2012,8, 2124–2131, doi:10.3762/bjoc.8.239
-diaminocarboxylamides was optimized, which resulted in Nα-deprotected syn-γ-chloro-α,β-diaminocarboxylamides, N-sulfinyl-β,γ-aziridino-α-aminocarboxylamide derivatives, a trans-imidazolidine, and an Nα,Nβ-deprotected syn-γ-chloro-α,β-diaminocarboxylamide.
Keywords: asymmetric synthesis; diaminoacidderivatives