化学
碳阳离子
反应性(心理学)
环加成
亲核细胞
电泳剂
立体化学
组合化学
基质(水族馆)
亲核芳香族取代
酒
药物化学
计算化学
亲核取代
极化(电化学)
戒指(化学)
作者
Yuchen Wang,Lin Zheng,Xin Liu,Chi Zhang,Yongjiu Li,Qiying Li,Xingyu Zhang,Wei Lin,Chenguang Liu
标识
DOI:10.1002/anie.202523632
摘要
Bicyclo[1.1.0]butane (BCB) has been widely explored as a scaffold for constructing 3D bioisosteres of benzene, owing to its olefin-like reactivity and ability to undergo cycloaddition reactions. Herein, we report that BCB derivatives bearing β-positioned hydroxyl or tosylamino groups (i.e., α-BCB alcohols or amines) undergo an unusual iodine(I)-mediated 4-endo cyclization to afford 2-oxabicyclo[2.1.1]hexanes and 2-azabicyclo[2.1.1]hexanes (BCHs). This strategy addresses a major limitation of prior BCHs synthesis, which typically require substrates tethered to carbonyl groups or aromatic rings to enable electronic polarization or photo-excitability. By circumventing this requirement, our method significantly broadens the range of substituents that can be incorporated into the BCH framework. Additionally, the transformation features practical advantages, including straightforward one-step substrate preparation, mild reaction conditions, and rapid kinetics-often completing within minutes. Mechanistic studies suggest that the 4-endo cyclization proceeds via an iodonium-induced carbocation intermediate, which is intramolecularly trapped by the nucleophilic ─OH or ─NHTs group.
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