861432-40-8Relevant academic research and scientific papers
Proline-β3-amino-ester dipeptides as efficient catalysts for enantioselective direct aldol reaction in aqueous medium
De Nisco, Mauro,Pedatella, Silvana,Ullah, Hidayat,Zaidi, Javid H.,Naviglio, Daniele,Oezdamar, Oezguer,Caputo, Romualdo
supporting information; experimental part, p. 9562 - 9565 (2010/03/04)
(Chemical Equation Presented) Dipeptides obtained from L-proline and β3-L-amino acids are reported to catalyze enantioselective direct aldol reaction in aqueous medium, leading to significant anti: syn diastereomeric ratios and enantiomeric exc
Efficient synthesis of orthogonally protected anti-2,3-diamino acids
Capone, Stefania,Guaragna, Annalisa,Palumbo, Giovanni,Pedatella, Silvana
, p. 6575 - 6579 (2007/10/03)
An asymmetric synthesis of anti-2,3-diamino acids is reported. The enolates of N,N-dibenzylated β3-amino esters were treated with di-tert-butyl azodicarboxylate (DBAD) to afford their N′,N″-di-Boc- 2-hydrazino derivatives with excellent anti di
