Functionalized styrene synthesis via palladium-catalyzed C C cleavage of aryl ketones
Tetrahedron Letters, ISSN: 0040-4039, Vol: 95, Page: 153721
2022
- 4Citations
- 1Captures
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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
We report herein the synthesis of functionalized styrenes via palladium-catalyzed Suzuki–Miyaura cross-coupling reaction between aryl ketone derivatives and potassium vinyltrifluoroborate. The employment of pyridine-oxazoline ligand was the key to the cleavage of unstrained C C bond. A variety of functional groups and biologically important moleculars were well tolerated. The orthogonal Suzuki–Miyaura coupling demonstrated the synthetic practicability.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0040403922001113; http://dx.doi.org/10.1016/j.tetlet.2022.153721; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85126544407&origin=inward; https://linkinghub.elsevier.com/retrieve/pii/S0040403922001113; https://dx.doi.org/10.1016/j.tetlet.2022.153721
Elsevier BV
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