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Traceless Redox-Annulations of Alicyclic Amines
Amines such as 1,2,3,4-tetrahydroisoquinoline undergo redox-neutral annulations with ortho-(nitromethyl)benzaldehyde. Benzoic acid acts as a promoter in these reactions, which involve concurrent amine α-C–H bond and N–H bond functionalization. Subsequent removal of the nitro group provides access to...
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| Publicat a: | SynOpen |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8318209/ https://ncbi.nlm.nih.gov/pubmed/34327302 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0040-1706004 |
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