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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Vydáno v:J Org Chem
Hlavní autoři: Brooks, Joshua L., Xu, Liping, Wiest, Olaf, Tan, Derek S.
Médium: Artigo
Jazyk:Inglês
Vydáno: American Chemical Society 2016
On-line přístup: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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