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一种用于定点功能化多肽的合成方法:无金属、高活性、在室温下具有选择性。

A Synthetic Method for Site-Specific Functionalized Polypeptides: Metal-Free, Highly Active, and Selective at Room Temperature.

机构信息

College of Bioresources Chemical and Materials Engineering, Shaanxi University of Science and Technology, Xi'an, 710021, People's Republic of China.

Department of Chemical Engineering, University of New Brunswick, Fredericton, New Brunswick, E3B 5A3, Canada.

出版信息

Angew Chem Int Ed Engl. 2021 Jan 11;60(2):889-895. doi: 10.1002/anie.202009316. Epub 2020 Nov 3.

Abstract

Functionalized polypeptides have attracted tremendous interest in recent years and found many stimulating applications owing to their tunable physicochemical characteristics including hydrophilicity and stimuli-responsive behavior. The development of new strategies to produce these polymers without metallic contaminants is crucial for their applications in high-value and sensitive domains, such as biomedical, microelectronic, food-packaging, and personal beauty care fields. Herein, a highly efficient strategy to access well-defined site-specific functionalized polypeptides is developed by combining Michael reaction with hydrogen-bonding organocatalytic ROP of NCA. A library of chain-end and chain-middle functionalized polypeptides (14 examples) with predesigned molecular weights and low polydispersities are readily prepared with this approach. Specifically, the whole synthetic process is metal-free, fulfilling high activity and selectivity at room temperature.

摘要

近年来,功能化多肽由于其可调的物理化学特性,包括亲水性和刺激响应性,引起了极大的关注,并找到了许多令人兴奋的应用。开发生产这些聚合物而不含有金属污染物的新策略对于它们在高价值和敏感领域的应用至关重要,例如生物医学、微电子、食品包装和个人美容护理领域。在此,通过迈克尔加成反应与 NCA 的氢键有机催化 ROP 相结合,开发了一种高效的制备具有明确的定点功能化多肽的策略。通过这种方法可以很容易地制备具有预定分子量和低多分散性的端基和链中功能化多肽库(14 个实例)。具体来说,整个合成过程是无金属的,在室温下具有高活性和选择性。

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