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AIBN initiated functionalization of the benzylic sp3 CH and CC bonds in the presence of dioxygen
Tetrahedron Letters ( IF 1.8 ) Pub Date : 2021-01-12 , DOI: 10.1016/j.tetlet.2020.152806
Yingying Hu , Yu Shao , Shuwei Zhang , Yuan Yuan , Zheng Sun , Yu Yuan , Xiaodong Jia

A sp3 Csingle bondH bond functionalization and Csingle bondC bond cleavage were realized by AIBN/O2 catalyst system, providing a series of benzophenones under mild reaction conditions. The mechanistic study shows that a peroxide intermediate is involved in this transformation, and in the case of diphenylmethanes, the sp3 Csingle bondC bond is cleaved through the peroxide rearrangement, which might provides a new way to cleave relatively strong Csingle bondC bond and be applied to more general Csingle bondC bond activation.



中文翻译:

AIBN在存在双氧的情况下引发了苄基sp 3 C 单键H和C 单键C键的官能化

通过AIBN / O 2催化剂体系实现了sp 3 C 单键H键的官能化和C 单键C键的裂解,在温和的反应条件下提供了一系列的二苯甲酮。机理研究表明,过氧化物中间体参与了这一转变,在二苯基甲烷的情况下,sp 3 C C键通过过氧化物重排而断裂,这可能提供了一种断裂相对较强的C C键并被应用的新方法。更一般的C C键活化。单键单键单键

更新日期:2021-02-26
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