Department of Chemistry, Saint Louis University, 3501 Laclede Ave, St. Louis, Missouri, 63103, United States.
Department of Chemistry, Southern Illinois University Edwardsville, 1 Hairpin Dr., Edwardsville, IL, 62025, United States.
Carbohydr Res. 2024 Apr;538:109102. doi: 10.1016/j.carres.2024.109102. Epub 2024 Mar 27.
The classical Koenigs-Knorr glycosidation of bromides or chlorides promoted with AgO or AgCO works only with reactive substrates (ideally both donor and acceptor). This reaction was found to be practically ineffective with unreactive donors such as per-O-benzoylated mannosyl bromide. Recently, it was discovered that the addition of catalytic (Lewis) acids to a silver salt-promoted reaction has a dramatic effect on the reaction rate and yield. A tentative mechanism for this cooperatively-catalyzed glycosylation reaction has been proposed, and the improved understanding of the reaction led to more efficient protocols and broader applications to a variety of glycosidic linkages. Since AgO-mediated activation was introduced by German chemists Koenigs and Knorr, and "cooperatively catalyzed" is Kooperativ Katalysiert in German, we refer to this new reaction as "the 4K reaction."
经典的 Koenigs-Knorr 糖苷化反应,使用 AgO 或 AgCO 作为促进剂,只能与反应性底物(理想情况下是供体和受体)发生反应。对于像全-O-苯甲酰化的甘露基溴化物这样的非反应性供体,该反应实际上是无效的。最近,人们发现,向银盐促进的反应中添加催化(路易斯)酸对反应速率和产率有显著影响。已经提出了这种协同催化糖苷化反应的暂定机制,对反应的深入理解导致了更有效的方案,并扩展到各种糖苷键的应用。由于德国化学家 Koenigs 和 Knorr 引入了 AgO 介导的活化,并且“协同催化”在德语中是 Kooperativ Katalysiert,因此我们将这个新反应称为“4K 反应”。