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Diastereoselective Synthesis of Highly Substituted Tetrahydrofurans by Pd-Catalyzed Tandem Oxidative Cyclization–Redox Relay Reactions Controlled by Intramolecular Hydrogen Bonding
[Image: see text] Palladium-catalyzed oxidative cyclization of alkenols provides a convenient entry into cyclic ethers but typically proceeds with little or no diastereoselectivity for cyclization of trisubstituted olefins to form tetrahydrofurans due to the similar energies of competing 5-membered...
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| Veröffentlicht in: | J Org Chem |
|---|---|
| Hauptverfasser: | , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
American Chemical
Society
2016
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| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5224347/ https://ncbi.nlm.nih.gov/pubmed/28004933 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.joc.6b02053 |
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