Journal
ORGANIC LETTERS
Volume 18, Issue 8, Pages 1896-1899Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b00672
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Funding
- Temple University
- Temple University Future Faculty Fellowship
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A facile method for the synthesis of challenging medium-sized cyclic ethers has been developed via a novel oxidative rearrangement of benzylic tertiary alcohols. The reaction provides access to cyclic acetals with diverse substitution at both C2 and the aromatic ring. The unique reactivity is enabled by poly(cationic) hypervalent iodine reagents and represents the first synthetic application of this underexplored class of compounds.
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