首页> 外文期刊>Protein and Peptide Letters >Click Chemistry Aided Synthesis of 1,4-Substituted 1,2,3-Triazole Based N-Fmoc Protected -Amino Acids: Isolation, Characterization and Synthesis of Novel Triazole Based Unnatural Amino Acids
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Click Chemistry Aided Synthesis of 1,4-Substituted 1,2,3-Triazole Based N-Fmoc Protected -Amino Acids: Isolation, Characterization and Synthesis of Novel Triazole Based Unnatural Amino Acids

机译:点击化学辅助1,4-取代的1,2,3-三唑基N-Fmoc保护的氨基酸的合成:新型三唑基非天然氨基酸的分离,表征和合成

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摘要

A new class of 1,4-substituted 1,2,3-triazole-based unnatural amino acids is demonstrated by employing click reaction between N-Fmoc amino alkyl azides and propiolic acid. The resulting unnatural amino acids were isolated and then subjected to Fmoc deprotection to isolate 1,2,3-triazole based amino acids as stable solids. These new class of molecules were also used for chain extension from both N- and C-terminals to synthesize dipeptidomimetics bearing 1,2,3- triazole moiety in the backbone.
机译:通过使用N-Fmoc氨基烷基叠氮化物和丙酸之间的点击反应,证明了一种新的基于1,4-取代的1,2,3-三唑的非天然氨基酸。分离得到的非天然氨基酸,然后进行Fmoc脱保护以分离出1,2,3-三唑基氨基酸为稳定固体。这些新型分子也用于从N端和C端进行链延伸,以合成在骨架上带有1,2,3-三唑部分的二肽模拟物。

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