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Allylic Substitution vs. Suzuki Cross-Coupling: Capitalizing on Chemoselectivity with Bifunctional Substrates

[Image: see text] One catalyst, two reactions; a tale of chemoselectivity: Given the choice between an allylic acetate and a vinylboronate ester, palladium preferentially reacts with the allylic acetate giving the allylic substitution product. In the presence of an aryl bromide and base, Suzuki cros...

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Autori principali: Hussain, Mahmud M., Walsh, Patrick J.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2010
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2917587/
https://ncbi.nlm.nih.gov/pubmed/20135655
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/anie.200905399
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