Potassium iodide as iodinating reagent: Rhodium(III)-catalyzed versatile and practical ortho -iodination of benzoic acids
Tetrahedron Letters, ISSN: 0040-4039, Vol: 140, Page: 155019
2024
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Article Description
A mild and efficient catalytic method for the iodination of benzoic acids has been explored. The catalytic system comprising [RhCp*Cl 2 ] 2 and PhI(OAc) 2 allowed the ortho -selective iodination products in the absence of any additive or base. This protocol features relatively broad substrate scope and operational simplicity. Air and moisture are also well tolerated. Importantly, readily available and cheap potassium iodide served as iodinating reagent.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S004040392400114X; http://dx.doi.org/10.1016/j.tetlet.2024.155019; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85188820712&origin=inward; https://linkinghub.elsevier.com/retrieve/pii/S004040392400114X; https://dx.doi.org/10.1016/j.tetlet.2024.155019
Elsevier BV
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