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Published in last 50 years
AbstractThe lactones (Ia) ‐ (Ic) and (Ie) are consecutively treated with lithium hexamethyldisilazide and N‐phenyltriflimide (II), forming the enol triflates (III).
Abstract Lactone enolates were treated with N-phenyl triflimide in the presence of hexamethylphosphoric triamide to afford smoothly the corresponding enol triflates, which, on reaction with lithium dialkylcuprates, gave rise to alkylated cyclic ethers in good yields.
Conversion of lactones into ethers