化学
胺化
分子内力
位阻效应
催化作用
立体专一性
氢化物
试剂
分子内反应
药物化学
光化学
立体化学
有机化学
氢
作者
Chendan Zhu,Yong Fang Liang,Xin Hong,Heqing Sun,Wei‐Yin Sun,Kendall N. Houk,Zhuangzhi Shi
摘要
A new strategy is reported for intramolecular sp(3) C-H amination under mild reaction conditions using iodoarene as catalyst and m-CPBA as oxidant. This C-H functionalization involving iodine(III) reagents generated in situ occurs readily at sterically hindered tertiary C-H bonds. DFT (M06-2X) calculations show that the preferred pathway involves an iodonium cation intermediate and proceeds via an energetically concerted transition state, through hydride transfer followed by the spontaneous C-N bond formation. This leads to the experimentally observed amination at a chiral center without loss of stereochemical information.
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