Single-Step, Rapid, and Mild Synthesis of β-Amino Acid N-Carboxy Anhydrides Using Micro-Flow Technology

被引:15
|
作者
Sugisawa, Naoto [1 ,2 ]
Otake, Yuma [1 ,2 ]
Nakamura, Hiroyuki [1 ]
Fuse, Shinichiro [1 ,3 ]
机构
[1] Tokyo Inst Technol, Inst Innovat Res, Lab Chem & Life Sci, Midori Ku, 4259 Nagatsuta Cho, Yokohama, Kanagawa 2268503, Japan
[2] Tokyo Inst Technol, Sch Life Sci & Technol, Midori Ku, 4259 Nagatsuta Cho, Yokohama, Kanagawa 2268503, Japan
[3] Nagoya Univ, Grad Sch Pharmaceut Sci, Dept Basic Med Sci, Chikusa Ku, Nagoya, Aichi 4648601, Japan
基金
日本学术振兴会;
关键词
acylation; anhydrides; flow chemistry; beta-amino acids; INITIATED POLYMERIZATION; NCA POLYMERIZATION; FLASH CHEMISTRY; BASE STRENGTHS; PEPTIDES; MECHANISM; LEUCINE; DESIGN;
D O I
10.1002/asia.201901429
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
beta-Amino acid N-carboxy anhydrides (beta-NCAs) are rarely used in the synthesis of beta-peptides, which is due mainly to the poor availability of these potentially useful substrates. Herein, we describe the heretofore challenging synthesis of beta-NCAs via a single-step, rapid, and mild formation using pH flash switching and flash dilution, which are aspects of micro-flow technology. We synthesized 15 beta-NCAs in good to excellent yields that included acid-labile beta-NCAs that cannot be readily synthesized using the conventional Leuchs approach. Scaled-up synthesis using this process can be readily achieved via continuous operation.
引用
收藏
页码:79 / 84
页数:6
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