Key Laboratory of Combinatorial Biosynthesis and Drug Discovery (Wuhan University), Ministry of Education, and Wuhan University School of Pharmaceutical Sciences, Wuhan 430071 (China).
Angew Chem Int Ed Engl. 2015 Mar 16;54(12):3763-7. doi: 10.1002/anie.201410309. Epub 2015 Feb 4.
A macrocyclic sulfate (MCS)-based approach to monodisperse poly(ethylene glycols) (M-PEGs) and their monofunctionalized derivatives has been developed. Macrocyclization of oligo(ethylene glycols) (OEGs) provides MCS (up to a 62-membered macrocycle) as versatile precursors for a range of monofunctionalized M-PEGs. Through iterative nucleophilic ring-opening reactions of MCS without performing group protection and activation, a series of M-PEGs, including the unprecedented 64-mer (2850 Da), can be readily prepared. Synthetic simplicity coupled with versatility of this new strategy may pave the way for broader applications of M-PEGs.
已开发出一种基于大环硫酸盐(MCS)的单分散聚乙二醇(M-PEG)及其单官能化衍生物的方法。寡聚乙二醇(OEG)的大环化提供了 MCS(高达 62 元大环),作为各种单官能化 M-PEG 的通用前体。通过在不进行基团保护和活化的情况下对 MCS 进行反复亲核开环反应,可以轻松制备一系列 M-PEG,包括前所未有的 64 元(2850 Da)PEG。这种新策略的合成简单性和多功能性可能为 M-PEG 的更广泛应用铺平道路。