Cargando…
Reversal of reaction type selectivity by Lewis acid coordination: the ortho photocycloaddition of 1- and 2-naphthaldehyde
The value of a specific substrate class for synthetic applications is greatly enhanced if different types of reactions can be performed selectively upon a judicious choice of reaction conditions. In the present study it was shown that the typical photochemical behaviour of naphthaldehydes is complet...
Autores principales: | Stegbauer, Simone, Jeremias, Noah, Jandl, Christian, Bach, Thorsten |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839505/ https://www.ncbi.nlm.nih.gov/pubmed/31803430 http://dx.doi.org/10.1039/c9sc03315g |
Ejemplares similares
-
Enantioselective Lewis Acid Catalyzed ortho Photocycloaddition of Olefins to Phenanthrene‐9‐carboxaldehydes
por: Stegbauer, Simone, et al.
Publicado: (2018) -
Enantioselective crossed intramolecular [2+2] photocycloaddition reactions mediated by a chiral chelating Lewis acid
por: Rigotti, Thomas, et al.
Publicado: (2022) -
Chiral Lewis acid catalysis in a visible light-triggered cycloaddition/rearrangement cascade
por: Stegbauer, Simone, et al.
Publicado: (2022) -
Arene Activation through Iminium Ions: Product Diversity from Intramolecular Photocycloaddition Reactions
por: Proessdorf, Johanna, et al.
Publicado: (2022) -
Overcoming peri- and ortho-selectivity in C–H methylation of 1-naphthaldehydes by a tunable transient ligand strategy
por: Mao, Yujian, et al.
Publicado: (2022)