名称:
                                A concise synthesis of aza-dipeptide isosteres
                             
                            
                                摘要:
                                Aza-dipeptide isosteres as potent HIV-protease inhibitors containing a (hydroxyethyl)-hydrazine moiety are synthesised in >98% diastereomeric and enantiomeric purity starting from (L)-phenylalanine aldehyde. (C) 1998 Elsevier Science Ltd. All rights reserved.
                             
                                                            
                                    DOI:
                                    10.1016/s0040-4039(98)00897-1