Cargando…
Stereoselective Formation of Substituted 1,3-Dioxolanes through a Three-Component Assembly during the Oxidation of Alkenes with Hypervalent Iodine(III)
Stereoselective formation of substituted 1,3-dioxolanes was achieved through an assembly of three components: alkene, carboxylic acid and silyl enol ether. The reaction proceeded via stereospecific generation of a 1,3-dioxolan-2-yl cation intermediate during oxidation of alkene substrates with hyper...
Autores principales: | Shimogaki, Mio, Fujita, Morifumi, Sugimura, Takashi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332268/ https://www.ncbi.nlm.nih.gov/pubmed/26393548 http://dx.doi.org/10.3390/molecules200917041 |
Ejemplares similares
-
Enantioselective dioxytosylation of styrenes using lactate-based chiral hypervalent iodine(III)
por: Fujita, Morifumi, et al.
Publicado: (2018) -
Recent advances in hypervalent iodine(III)-catalyzed functionalization of alkenes
por: Li, Xiang, et al.
Publicado: (2018) -
Thioamination of Alkenes with Hypervalent Iodine Reagents
por: Mizar, Pushpak, et al.
Publicado: (2016) -
Copper-catalyzed aminoalkynylation of alkenes with hypervalent iodine reagents
por: Shen, Kun, et al.
Publicado: (2017) -
Hypervalent Iodine
por: Kotali, Antigoni
Publicado: (2005)