Synthesis of peptide derived amino alcohols II. Synthetic methodology for the preparation of tertiary alcohols
作者:Jollie D. Godfrey、Eric M. Gordon、Derek J. Von Langen
DOI:10.1016/s0040-4039(00)95370-x
日期:1987.1
Synthetic methods are described for the preparation of a series of tripeptide derived aminoalcohols (i.e.,). These novel peptidyl tertiary alcohols are potential inhibitors of angiotensin converting enzyme (ACE). The synthetic targets resemble acyltripeptide substrates for the enzyme, but contain a -CHOH(CH3)-CH2-NH- moiety, as replacement for the scissile amide bond.
描述了用于制备一系列三肽衍生的氨基醇(即,)的合成方法。这些新型肽基叔醇是血管紧张素转化酶(ACE)的潜在抑制剂。合成靶标类似于该酶的酰基三肽底物,但是含有-CHOH(CH 3)-CH 2 -NH-部分,作为可裂解酰胺键的替代物。