Cargando…
Intramolecular azavinyl carbene-triggered rearrangement of furans
An intramolecular rhodium-catalyzed reaction of 1-tosyl-1,2,3-triazoles with furans has been explored. The tosylimino functionality was found to play a significant chemical role participating in the subsequent domino-transformations of a key reaction intermediate. One of the reaction pathways leads...
Autores principales: | Makarov, Anton S., Uchuskin, Maxim G., Hashmi, A. Stephen K. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839507/ https://www.ncbi.nlm.nih.gov/pubmed/31803433 http://dx.doi.org/10.1039/c9sc02299f |
Ejemplares similares
-
Intramolecular photochemical [2 + 1]-cycloadditions of nucleophilic siloxy carbenes
por: Bunyamin, Amanda, et al.
Publicado: (2022) -
Intramolecular crankshaft-type rearrangement in a photoisomerised glycoconjugate
por: Hricovíni, Michal, et al.
Publicado: (2023) -
Palladium-catalyzed intramolecular enantioselective C(sp(3))–H insertion of donor/donor carbenes
por: Li, Wendeng, et al.
Publicado: (2022) -
Methanol-Driven Oxidative Rearrangement of Biogenic Furans – Enzyme Cascades vs. Photobiocatalysis
por: Jäger, Christina, et al.
Publicado: (2021) -
Rh(2)(ii)-catalyzed enantioselective intramolecular Büchner reaction and aromatic substitution of donor–donor carbenes
por: Zhu, Dong, et al.
Publicado: (2022)