作者:Livia G. Boros、Bart De Corte、Rayomand H. Gimi、John T. Welch、Yang Wu、Robert E. Handschumacher
DOI:10.1016/0040-4039(94)88067-0
日期:1994.8
Fluoroolefin dipeptide isosteres were synthesized applying the Peterson reaction as a novel method for fluoroolefination. The dipeptide isosteres were elaborated to provide the conformationally constrained analogs (1-(R), 1-(S) and 2-(R), 2-(S)) of the Suc-Ala-Gly-Pro-Phe-pNA tetrapeptide, a synthetic substate of cyclophilin.
应用Peterson反应合成氟代烯烃二肽等排体作为一种新的氟代烯烃聚合方法。精心制作了二肽等位基因,以提供Suc-Ala-Gly-Pro-Phe-pNA四肽的构象受限类似物(1-(R),1-(S)和2-(R),2-(S)) ,是亲环蛋白的合成亚状态。