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- W4280492529 abstract "Abstract Herein we disclose a mild protocol for the reductive functionalisation of quinolinium and isoquinolinium salts. The reaction proceeds under transition‐metal‐free conditions as well as under rhodium catalysis with very low catalyst loadings (0.01 mol %) and uses inexpensive formic acid as the terminal reductant. A wide range of electrophiles, including enones, imides, unsaturated esters and sulfones, β‐nitro styrenes and aldehydes are intercepted by the in situ formed enamine species forming a large variety of substituted tetrahydro(iso)quinolines. Electrophiles are incorporated at the C‐3 and C‐4 position for quinolines and isoquinolines respectively, providing access to substitution patterns which are not favoured in electrophilic or nucleophilic aromatic substitution. Finally, this reactivity was exploited to facilitate three types of annulation reactions, giving rise to complex polycyclic products of a formal [3+3] or [4+2] cycloaddition." @default.
- W4280492529 created "2022-05-22" @default.
- W4280492529 creator A5013585464 @default.
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- W4280492529 creator A5089206379 @default.
- W4280492529 date "2022-05-13" @default.
- W4280492529 modified "2023-09-26" @default.
- W4280492529 title "Evolution of the Dearomative Functionalization of Activated Quinolines and Isoquinolines: Expansion of the Electrophile Scope" @default.
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- W4280492529 doi "https://doi.org/10.1002/ange.202204682" @default.
- W4280492529 hasPublicationYear "2022" @default.
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