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- W2952188942 abstract "Abstract The regio- and stereochemistry of the alkylation of dienediolates from unsaturated carboxylic acids with benzylic halides, which often results in mixtures of isomers, can be controlled by means of changes in the lithium amide, allowing the α-regioisomer to be obtained as the major diastereoisomer. In addition, when chiral amines are used, moderate enantiomeric excesses can be attained." @default.
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- W2952188942 date "2010-05-24" @default.
- W2952188942 modified "2023-09-26" @default.
- W2952188942 title "ChemInform Abstract: Enantioselective α-Alkylation of Unsaturated Carboxylic Acids Using a Chiral Lithium Amide." @default.
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- W2952188942 doi "https://doi.org/10.1002/chin.200137031" @default.
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