ChemInform Abstract: 8-Fluoro-6-(methoxymethoxy)quinoline: Synthesis and Regioselective Functionalization via Reaction with Organolithium Compounds.
β Scribed by J. STADLWIESER; P. BARBIER; S. TAYLOR
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 37 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
8-Fluoro-6-(methoxymethoxy)quinoline: Synthesis and Regioselective Functionalization via Reaction with Organolithium Compounds. -The reactivity of title compound (IX) with organo-Li compounds is studied. Based on the results, a short synthesis of highly functionalized quinolines such as (XVIII) is developed. -(STADLWIESER,
π SIMILAR VOLUMES
Synthesis of N-Alkoxycarbonyl-3-substituted Tetramic Acids and Functionalized Enols via C-Acylation Reactions of Active Methylene Compounds with N-Hydroxysuccinimide Esters of N-AlkoxycarbonylΞ±-amino Acids. -A new, mild, and advantageous approach is used for the preparation of the title compounds,