Spiroketals via oxidative rearrangement of enol ethers?
Organic & Biomolecular Chemistry Pub Date: 2006-11-14 DOI: 10.1039/B612992G
Abstract
Oxidative rearrangement of cyclic enol ethers leads to α-alkoxyesters. In the presence of a neighboring spiroether, this approach provides a stereoselective access to spiroketals. A modified proposal for the biosynthesis of
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Journal Name：Organic & Biomolecular Chemistry
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CAS no.: 89640-58-4
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