Shiina Isamu, Ushiyama Hisaya, Yamada Yo-ko, Kawakita Yo-ichi, Nakata Kenya
Department of Applied Chemistry, Faculty of Science, Tokyo University of Science, Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan.
Chem Asian J. 2008 Feb 1;3(2):454-61. doi: 10.1002/asia.200700305.
Various carboxamides or peptides were synthesized from the corresponding carboxylic acids and amines or alpha-amino acids in high yields by the catalysis of 4-(dimethylamino)pyridine N-oxide (DMAPO) with 2-methyl-6-nitrobenzoic anhydride (MNBA). Because the segment-coupling reaction of alpha-amino acids proceeds through the effective activation of the carboxylic acid moieties with DMAPO in the presence of tertiary amines under mild conditions, undesired racemization was hardly observed in the synthesis of oligopeptides such as Z-Gly-Phe-Val-OMe, Z-Phe-Val-Ala-OMe, and Bz-Val-Val-OMe.
在2-甲基-6-硝基苯甲酸酐(MNBA)存在下,通过4-(二甲基氨基)吡啶N-氧化物(DMAPO)催化,由相应的羧酸与胺或α-氨基酸以高收率合成了各种羧酰胺或肽。由于α-氨基酸的片段偶联反应是在温和条件下,在叔胺存在下通过DMAPO对羧酸部分的有效活化进行的,因此在合成诸如Z-Gly-Phe-Val-OMe、Z-Phe-Val-Ala-OMe和Bz-Val-Val-OMe等寡肽时,几乎未观察到不希望的消旋化现象。