名称:
                                Synthesis of aspartimide-free protected peptides on base-labile functionalized resins
                             
                            
                                摘要:
                                Aspartimide prone sequence containing protected peptides are successfully synthesized in solid phase by using the bifunctional linker N-[(9-hydroxymethyl)-2-fluorenyl] succinamic acid (HMFS) in combination with morpholine as the cleavage reagent. Access to high purity peptide synthons opens a straightforward way to the synthesis of large proteins by convergent strategies. (C) 2000 Elsevier Science Ltd. All rights reserved.
                             
                                                            
                                    DOI:
                                    10.1016/s0040-4039(00)01398-8