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Enantioselective Synthesis of 2,2-Disubstituted Tetrahydrofurans by Palladium-Catalyzed [3+2] Cycloadditions of Trimethylenemethane with Ketones

[Image: see text] An approach to 2,2-disubstituted 4-methylenetetrahydrofurans has been developed utilizing a cycloaddition of trimethylenemethane with aryl ketones, with formation of the products in up to 96% yield and 95% ee. The reaction is catalyzed by palladium in the presence of a phosphoramid...

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Bibliografski detalji
Glavni autori: Trost, Barry M., Bringley, Dustin A.
Format: Artigo
Jezik:Inglês
Izdano: 2013
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3864557/
https://ncbi.nlm.nih.gov/pubmed/23495134
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/anie.201300616
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