双环分子
化学
立体化学
组合化学
化学合成
有机化学
钥匙(锁)
内酯
生物活性
立体异构
产量(工程)
反应条件
作者
Oleksandr Stashkevych,Volodymyr Kokhalskyi,Yevhenii Mynak,Vadym V. Levterov,Oleh Shablykin,Iryna Pishel,Pavel K. Mykhailiuk
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-09-22
卷期号:64 (46): e202517814-e202517814
被引量:7
标识
DOI:10.1002/anie.202517814
摘要
2-Azabicyclo[2.2.2]octanes have been designed, synthesized, and validated biologically as isosteres of piperidine/pyridine. The key reaction step was the cyclization of cyclic alkenyl amines with the KOtBu/I2/CO2 combination. The method proved to be scalable (up to 20 g) and general: it was also applied for the synthesis of 2-azabicyclo[2.1.1]hexanes, 2-azabicyclo[3.1.1]heptanes, 2-azabicyclo[2.2.1]heptanes, 7-azabicyclo[2.2.1]heptanes, and 6-azabicyclo[3.2.1]octanes. Finally, combined with the nitrogen deletion tactic, this method also opened a practical way toward the previously hardly accessible 1,2-disubstituted bicyclo[1.1.1]pentanes-saturated analogues of ortho-benzenes.
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