作者:Alan R. Katritzky、Laszlo Urogdi、Annie Mayence
DOI:10.1039/c39890000337
日期:——
12), derived from benzotriazole (7), glyoxylic ester (6) or acid (11), and an amide (5), react with ammonia in a novel, convenient route to monoacylated α-aminoglycines (9,13) useful for the synthesis of peptide analogues.
加合物(8,12)中,从苯并三唑(衍生7),乙醛酸酯(6)或酸(11),和酰胺(5),与氨反应以一种新颖的,向单酰化α-aminoglycines(方便的途径9,13)可用于肽类似物的合成。