Cargando…
Synthesis of functionalised isochromans: epoxides as aldehyde surrogates in hexafluoroisopropanol
The oxa-Pictet–Spengler reaction is arguably the most straightforward and modular way to construct the privileged isochroman motif, but its scope is largely limited to benzaldehyde derivatives and to electron-rich β-phenylethanols that lack substitution along the aliphatic chain. Here we describe a...
Autores principales: | Muller, Cyprien, Horký, Filip, Vayer, Marie, Golushko, Andrei, Lebœuf, David, Moran, Joseph |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10016621/ https://www.ncbi.nlm.nih.gov/pubmed/36937595 http://dx.doi.org/10.1039/d2sc06692k |
Ejemplares similares
-
Ring-opening hydroarylation of monosubstituted cyclopropanes enabled by hexafluoroisopropanol
por: Richmond, Edward, et al.
Publicado: (2018) -
Aromatic C–H amination in hexafluoroisopropanol
por: D'Amato, Erica M., et al.
Publicado: (2019) -
Enantioselective synthesis of isochromans and tetrahydroisoquinolines by C–H insertion of donor/donor carbenes
por: Nickerson, Leslie A., et al.
Publicado: (2019) -
Correction: Enantioselective synthesis of isochromans and tetrahydroisoquinolines by C–H insertion of donor/donor carbenes
por: Nickerson, Leslie A., et al.
Publicado: (2020) -
Redox-triggered cascade dearomative cyclizations enabled by hexafluoroisopropanol
por: Li, Shuai-Shuai, et al.
Publicado: (2018)