677717-66-7Relevant academic research and scientific papers
Diastereoselective synthesis of enantioenriched homopropargyl amino alcohols from α-dibenzylamino aldehydes and their use as chiral synthons
Andrés, José M.,Pedrosa, Rafael,Pérez-Encabo, Alfonso,Ramírez, María
, p. 7783 - 7792 (2007/10/03)
Homochiral α-dibenzylamino aldehydes, prepared from the corresponding α-amino acids, react with propargyl bromide and zinc in DMF/THF (1:1) or DMF/Et2O (1:1) at 20 °C to afford, in good yields and dr, homopropargylic 1,2-amino alcohols. anti Di
Diastereoselective aldol reaction of N,N-dibenzyl-α-amino aldehydes with ketones catalyzed by proline
Pan, Qiangbiao,Zou, Benli,Wang, Yuji,Ma, Dawei
, p. 1009 - 1012 (2007/10/03)
(Equation presented) L-Proline-catalyzed direct aldol reaction of L-amino acid-derived N,N-dibenzyl amino aldehydes with acetone, cyclopentanone, or hydroxyacetone provides γ-amino-β-hydroxy- or γ-amino-α, β-dihydroxy-ketones with moderate to excellent yi
