基 () 氨基酸和:立体选择性合成和光特性
Mathieu Arribat1, Emmanuelle Rémond1, Sébastien Clément2
1Institut des Biomolécules Max Mousseron, IBMM, UMR 5247, CNRS, Université de Montpellier, ENSCM , Place Eugène Bataillon, 34095 Montpellier cedex 5, France.
Journal of the American Chemical Society
|December 22, 2017
概括
通过立体选择合成了新的胺氨基酸. 这些新型非自然氨基酸提供多样化的侧链,并表现出用于标记和结构-活性关系研究的有用光特性.
科学领域:
- 有机化学
- 医学化学
- 生物化学
背景情况:
- 不自然的氨基酸对于扩大的化学多样性至关重要.
- 开发具有独特功能的新型氨基酸,如光,是活跃的研究领域.
研究的目的:
- 通过立体选择性合成新型基氨基酸.
- 探索这些新氨基酸的衍生潜力和光特性.
- 证明它们被纳入的潜在应用.
主要方法:
- 通过与α-氨基反应进行立体选择性合成.
- 在现场与复合.
- 选择性去保护和合 (C-或N-).
主要成果:
- 成功合成具有多种侧链可能性的基氨基酸.
- 通过标准合技术将其纳入.
- 观测到具有很大的斯托克斯转移 (160 nm) 和高达535 nm的发射的光特性.
结论:
- 酸 () 氨基酸代表了一类新的非天然氨基酸.
- 这些化合物是创建功能化的通用构件.
- 它们的光特性使得它们成为标记开发和SAR研究的有希望的候选者.
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