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para‐Selective Benzylation of Aryl Iodides by the in situ Preparation of ArIF2: a Hypervalent Iodine‐Guided Electrophilic Substitution
European Journal of Organic Chemistry ( IF 2.8 ) Pub Date : 2020-04-09 , DOI: 10.1002/ejoc.202000393
Jennifer Noorollah 1 , Haram Im 1 , Fatima Siddiqi 1 , Nirvanie Singh 1 , Nicholas R. Spatola 1 , Azka Chaudhry 1 , Taro J. Jones 1 , I. F. Dempsey Hyatt 1
Affiliation  

Delving into the HIGES: Hypervalent iodine‐guided electrophilic substitution (HIGES) was described previously for the para‐selective benzylation of aryl‐λ3‐iodane diacetates. To make our methodology more accessible to the synthetic community, a procedure was developed in which the benzylation product can be afforded from an aryl iodide by an in situ oxidation with an overall higher yield for most substrates.
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中文翻译:

ArIF2的原位制备对碘化物的对位选择性苯甲酰化:高价碘引导的亲电取代

钻研HIGES:高价碘引导电取代(HIGES)是为先前所描述的对位芳-λ的-选择性苄3 -iodane二乙酸酯。为了使我们的方法更易于合成社区使用,开发了一种程序,其中可以通过原位氧化从芳基碘化物提供苄基化产物,大多数底​​物的总体收率更高。
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更新日期:2020-04-09
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