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• W2950697145 abstract "Regio- and stereocontrolled alkoxy mercuration of α,β-unsaturated esters allows direct access to 1,3-syn diols in good yields. Demercuration of adducts leads to 1,3 skipped dihydroxy esters, alcohols, and α-halo esters. The deprotection of acetonide with Amberlyst 15 on 1,3-syn-dihydroxy esters gives the corresponding δ-lactones." @default.
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• W2950697145 date "2008-09-01" @default.
• W2950697145 modified "2023-10-09" @default.
• W2950697145 title "Stereoselective synthesis of versatile 2-chloromercurium-3,5-syn-dihydroxy esters via intramolecular oxymercuration" @default.
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• W2950697145 doi "https://doi.org/10.1016/j.tet.2008.06.094" @default.
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