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- W2077499529 abstract "Abstract The sequence involving conjugate radical addition/aldol condensation/lactonization is a high yielding route to di- and tri-substituted γ-lactones starting from fumaric or maleic diesters. The reactions are mediated with dialkylzincs. The domino process relies on the ability of dialkylzinc to transform α-alkoxycarbonylalkyl radicals into zinc enolates. Compared to diethylzinc, dimethylzinc enables the use of a wider range of alkyl radical precursors. In addition, dimethylzinc is a convenient source of methyl radical, which leads to a straightforward synthesis of methylated derivatives related to α-methyl-paraconic acids." @default.
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- W2077499529 date "2007-05-01" @default.
- W2077499529 modified "2023-09-23" @default.
- W2077499529 title "α,β-Unsaturated Diesters: Radical Acceptors in Dialkylzinc-Mediated Tandem Radical Addition/Aldol Condensation. A Straightforward Synthesis of rac-Nephrosteranic Acid." @default.
- W2077499529 cites W2951755089 @default.
- W2077499529 doi "https://doi.org/10.1002/chin.200718109" @default.
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