Direct Disulfide Formation from 2-Quinolinylmethyl Thioethers with Iron(III) or Copper(II) Salt
作者:Hidenori Yoshizawa、Akira Otaka、Hiromu Habashita、Nobutaka Fujii
DOI:10.1246/cl.1993.803
日期:1993.5
2-Quinolinylmethyl thioethers were efficiently cleaved to generate the corresponding symmetrical disulfides using the following systems; FeCl3/N,N-dimethylformamide (DMF)/H2O, FeCl3/ethanol (EtOH)/H2O, and CuCl2/DMF/H2O. The 2-quinolinylmethyl group was utilized as a thiol protecting group in the synthesis of a model peptide.
使用以下系统有效地裂解 2-喹啉基甲基硫醚以生成相应的对称二硫化物;FeCl3/N,N-二甲基甲酰胺 (DMF)/H2O、FeCl3/乙醇 (EtOH)/H2O 和 CuCl2/DMF/H2O。在模型肽的合成中,2-喹啉基甲基被用作硫醇保护基团。