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Acetic Acid Promoted Redox Annulations with Dual C–H Functionalization
[Image: see text] Amines such as 1,2,3,4-tetrahydroisoquinoline undergo redox-neutral annulations with 2-alkylquinoline-3-carbaldehydes as well as the corresponding 4-alkyl isomers and pyridine analogues. These processes involve dual C–H bond functionalization. Acetic acid is used as a cosolvent and...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
American Chemical
Society
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460294/ https://www.ncbi.nlm.nih.gov/pubmed/28510444 http://dx.doi.org/10.1021/acs.orglett.7b01047 |