Hypervalent Iodine Oxidation of Trimethylsilyl Ketene Acetals: A Convenient Route to α-Methoxylation of Esters and Lactones
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397919708004187
Reference17 articles.
1. Carbon–carbon bond formation using hypervalent iodine under Lewis acid conditions: scope of the method for the synthesis of butane-1,4-diones
2. Hypervalent iodine oxidation of silyl enol ethers under Lewis-acid conditions in methanol. A general route to .alpha.-methoxy ketones
3. Reaction of [hydroxy(tosyloxy)iodo]benzene and [hydroxy(mesyloxy)iodo]benzene with trimethylsilyl enol ethers. A new general method for .alpha.-sulfonyloxylation of carbonyl compounds
4. Hypervalent iodine oxidation of trimethylsilyl enol ethers of ketones: A direct synthesis of α-keto triflates
5. Carbon-carbon bond formation in reactions of PhIO.cntdot.HBF4-silyl enol ether adduct with alkenes or silyl enol ethers
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