化学
环加成
组合化学
超分子化学
选择性
叠氮化物
亲核取代
分子识别
分子内力
亲核细胞
点击化学
催化作用
立体化学
分子
有机化学
作者
Surya Adhikari,Anji Chen,Guijun Wang
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2021-06-03
卷期号:26 (11): 3394-3394
被引量:4
标识
DOI:10.3390/molecules26113394
摘要
Glycomacrolactones exhibit many interesting biological properties, and they are also important in molecular recognitions and for supramolecular chemistry. Therefore, it is important to be able to access glycomacrocycles with different sizes and functionality. A new series of carbohydrate-based macrocycles containing triazole and lactone moieties have been designed and synthesized. The synthesis features an intramolecular nucleophilic substitution reaction for the macrocyclization step. In this article, the effect of some common sulfonate leaving groups is evaluated for macrolactonization. Using tosylate gave good selectivity for monolactonization products with good yields. Fourteen different macrocycles have been synthesized and characterized, of which eleven macrocycles are from cyclization of the C1 to C6 positions of N-acetyl D-glucosamine derivatives and three others from C2 to C6 cyclization of functionalized D-glucosamine derivatives. These novel macrolactones have unique structures and demonstrate interesting anion binding properties, especially for chloride. The macrocycles containing two triazoles form complexes with copper sulfate, and they are effective ligands for copper sulfate mediated azide-alkyne cycloaddition reactions (CuAAC). In addition, several macrocycles show some selectivity for different alkynes.
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