生物正交化学
叠氮化物
化学
环加成
反应速率
点击化学
组合化学
生物化学
有机化学
催化作用
作者
Jessica A. Stewart,Cody J. Wilson,Benjamin M. Swarts
标识
DOI:10.1080/07328303.2014.931963
摘要
AbstractThe strain-promoted azide–alkyne cycloaddition (SPAAC) is the most widely used bioorthogonal reaction for imaging azide-labeled glycans in living systems. Rapid SPAAC reactions are essential for visualizing biological processes that occur on a short timescale, and efforts to increase SPAAC reaction rates by modulating the cyclooctyne structure have been highly successful. However, optimizing azido sugar structure for improved SPAAC rates has not been explored. In this study, we show that altering azide position on the sugar ring can have a modest but significant impact on SPAAC reaction rate, which has implications for designing and interpreting experiments involving azide-specific bioorthogonal reactions.Keywords: Strain-promoted azide–alkyne cycloaddition (SPAAC)Copper-free click chemistryBioorthogonal chemistryReaction kinetics/rateAzido sugar
科研通智能强力驱动
Strongly Powered by AbleSci AI