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Redox-Annulations of Cyclic Amines with Electron-Deficient o-Tolualdehydes
[Image: see text] Amines such as 1,2,3,4-tetrahydroisoquinoline undergo redox-neutral annulations with 2-methyl-3,5-dinitrobenzaldehyde and closely related substrates. Acetic acid serves as the solvent and sole promoter of these transformations which involve dual C–H functionalization.
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| Veröffentlicht in: | Org Lett |
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| Hauptverfasser: | , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2019
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6526004/ https://ncbi.nlm.nih.gov/pubmed/30840479 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.orglett.9b00438 |
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