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邻苯并恶唑基亚氨基碳酸酯作为多功能糖基供体在化学糖苷化中的应用。

O-Benzoxazolyl imidates as versatile glycosyl donors for chemical glycosylation.

机构信息

Department of Chemistry and Biochemistry, University of Missouri - St. Louis, One University Boulevard, St. Louis, Missouri 63121, USA.

出版信息

Org Biomol Chem. 2013 Jun 28;11(24):4068-76. doi: 10.1039/c3ob40667a.

Abstract

Herein, we report a new class of glycosyl donors, benzoxazolyl imidates, for chemical glycosylation. The O-benzoxazolyl (OBox) leaving group was designed with an aim to compare the relative reactivity and stability of similarly structured S-benzoxazolyl (SBox) glycosides (thioimidates) developed in our lab and glycosyl trichloroacetimidates (TCAI, O-imidates) developed by Schmidt. Novel OBox donors can be activated under catalytic conditions and provided excellent yields in glycosylation. The OBox imidates were found to be more reactive than either SBox or TCAI donors. The high reactivity profile was confirmed in direct competitive experiments and was found beneficial for HPLC-assisted solid-phase synthesis.

摘要

在此,我们报告了一类新的糖基供体,苯并恶唑基亚氨酸酯,用于化学糖苷化。O-苯并恶唑基(OBox)离去基团的设计旨在比较我们实验室开发的类似结构的 S-苯并恶唑基(SBox)糖苷(硫亚氨酸酯)和 Schmidt 开发的糖基三氯乙酰亚氨酸酯(TCAI,O-亚氨酸酯)的相对反应性和稳定性。新型 OBox 供体可在催化条件下被激活,并在糖苷化中提供优异的产率。发现 OBox 亚氨酸酯比 SBox 或 TCAI 供体更具反应性。在直接竞争实验中证实了高反应性,并且发现这对 HPLC 辅助固相合成有益。

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