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- W2082220610 abstract "The intramolecular Michael addition of enantiomerically enriched γ-[(phenylthio)acyl]oxy, β-unsaturated esters opens a way to the synthesis of saturated γ-lactones,α-methylene butyrolactones and butenolides of high enantiomerical purity. The method is complemented by the alkylation of the obtained α-benzenesulfonyl-γ-lactones which with an unusual stereoselectivity leads tto a new methodology to obtain polysubstituted carbocycles of different size." @default.
- W2082220610 created "2016-06-24" @default.
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- W2082220610 date "2010-08-04" @default.
- W2082220610 modified "2023-09-26" @default.
- W2082220610 title "ChemInform Abstract: Stereoselective Synthesis of γ-Butyrolactones by Intramolecular Michael Addition" @default.
- W2082220610 cites W2951610796 @default.
- W2082220610 doi "https://doi.org/10.1002/chin.199715288" @default.
- W2082220610 hasPublicationYear "2010" @default.
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