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- W2892450135 endingPage "6238" @default.
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- W2892450135 abstract "A synthetic strategy for phenolic lipids such as anacardic acid and ginkgolic acid derivatives using an efficient and selective redox-relay Heck reaction followed by a stereoselective olefination is reported. This approach controls both the alkene position and stereochemistry, allowing the synthesis of natural and unnatural unsaturated lipids as single isomers. By this strategy, the activities of different anacardic acid and ginkgolic acid derivatives have been examined in a matrix metalloproteinase inhibition assay." @default.
- W2892450135 created "2018-10-05" @default.
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- W2892450135 date "2018-09-25" @default.
- W2892450135 modified "2023-10-18" @default.
- W2892450135 title "A Heck-Based Strategy To Generate Anacardic Acids and Related Phenolic Lipids for Isoform-Specific Bioactivity Profiling" @default.
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- W2892450135 doi "https://doi.org/10.1021/acs.orglett.8b02705" @default.
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