A LiCl‐Mediated Br/Mg Exchange Reaction for the Preparation of Functionalized Aryl‐ and Heteroarylmagnesium Compounds from Organic Bromides
Ludwig-Maximilians-Universität München
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Abstract
A wide range of aryl and heteroaryl bromides, which are usually sluggish in exchange reactions, are readily converted into the corresponding Grignard reagents by means of a Br/Mg exchange reaction triggered by iPrMgCl⋅LiCl (see scheme). These Grignard intermediates react with electrophiles in good yields. Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2004/z54084_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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Authors
2Topics & keywords
Topics
Keywords
- Aryl
- Electrophile
- Chemistry
- Reagent
- Combinatorial chemistry
- Organic synthesis
- Grignard reagent
- Reactivity (psychology)
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