Preparation of peptide thioesters using Fmoc strategy through hydroxyl side chain anchoring
摘要:
In the course of the chemical synthesis of human protein mitogaligin, we present here a simple method to prepare peptide thioesters using Fmoc chemistry. The hydroxyl side chain of serine was reacted with a trichloroacetimidate Wang resin to anchor it on solid phase. After peptide elongation and orthogonal unmasking of the C-terminus, the amino thioester was introduced under optimized conditions to avoid epimerization. (C) 2008 Elsevier Ltd. All rights reserved.
Preparation of peptide thioesters using Fmoc strategy through hydroxyl side chain anchoring
摘要:
In the course of the chemical synthesis of human protein mitogaligin, we present here a simple method to prepare peptide thioesters using Fmoc chemistry. The hydroxyl side chain of serine was reacted with a trichloroacetimidate Wang resin to anchor it on solid phase. After peptide elongation and orthogonal unmasking of the C-terminus, the amino thioester was introduced under optimized conditions to avoid epimerization. (C) 2008 Elsevier Ltd. All rights reserved.