参考标题:Fmoc-Amox, A Suitable Reagent For The Introduction Of Fmoc 作者:Ashish Kumar,Anamika Sharma,Elvira Haimov,Ayman El-Faham,Beatriz G. De La Torre,Fernando Albericio |发布日期:2017.10.20 摘要:Synthesis Of Most Peptides Is Achieved Using Solid-Phase Peptide Synthesis Employing The Fmoc/tert-Butyl Strategy. However, The Introduction Of Fmoc In N-Unprotected Amino Acids Seems To Be Challenging Due To The Formation Of Dipeptides And Sometimes Tripeptides As Impurities And β-Alanyl Impurities When Fmoc-Osu Is Used As Well. Herein, We Report An Efficient And Successful Method Using Fmoc-Amox
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