Breipohl G, Knolle J, König W
Klin Wochenschr. 1986;64 Suppl 6:16-20.
The synthesis of Atriopeptin III (AP III) was accomplished using fragment condensation and solid phase synthesis with Fmoc-groups as temporary and tert.-butyl-groups as permanent protection. Advantages and disadvantages of both methods are discussed.
使用片段缩合和以Fmoc基团作为临时保护基、叔丁基基团作为永久保护基的固相合成法完成了心房肽III（AP III）的合成。讨论了这两种方法的优缺点。
