Oxidative Ring Cleavage of Cyclic Acetals with Hypervalent tert-Butylperoxy-λ3-iodanes
Author:
Affiliation:
1. Faculty of Pharmaceutical Sciences, University of Tokushima, 1-78 Shomachi, Tokushima 770-8505, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol016202x
Reference28 articles.
1. A stable crystalline alkylperoxyiodinane: 1-(tert-butylperoxy)-1,2-benziodoxol-3(1H)-one
2. Hypervalent (tert-Butylperoxy)iodanes Generate Iodine-Centered Radicals at Room Temperature in Solution: Oxidation and Deprotection of Benzyl and Allyl Ethers, and Evidence for Generation of α-Oxy Carbon Radicals
3. Oxidation of Sulfides to Sulfoxides with Hypervalent (tert-Butylperoxy)iodanes
4. Free-radical oxidation of para-substituted phenols by hypervalent tert-butylperoxyiodane and tert-butyl hydroperoxide: Synthesis of 4-(tert-butylperoxy)-2,5-cyclohexadien-1-ones
5. Oxidation of Amines with Hypervalent tert-Butylperoxyiodanes: Synthesis of Imines and tert-Butylperoxyamino Acetals
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