Bodanszky M
Int J Pept Protein Res. 1985 May;25(5):449-74. doi: 10.1111/j.1399-3011.1985.tb02200.x.
An attempt was made to discern ideas and trends in the development of peptide synthesis and to recognize general principles of the discipline. Introduction of efficient methods of activation and coupling during the early years of the reviewed period was followed by only moderate further improvements. Major advances were achieved by the discovery of novel methods of protection and by techniques of facilitation. Improvements in the methods of deblocking hold considerable promise and might bring significantly closer the goal of peptide synthesis: the direct preparation of homogeneous products.
本文旨在梳理肽合成发展过程中的思想和趋势,并认识该学科的一般原则。在回顾期的早期引入高效的活化和偶联方法之后,后续仅取得了适度的进一步改进。主要进展是通过发现新的保护方法和促进技术实现的。去保护方法的改进具有很大的前景,可能会大大拉近肽合成的目标:直接制备均一产物。