Cargando…
Chemoselective palladium-catalyzed deprotonative arylation/[1,2]-Wittig rearrangement of pyridylmethyl ethers
Control of chemoselectivity is one of the most challenging problems facing chemists and is particularly important in the synthesis of bioactive compounds and medications. Herein, the first highly chemoselective tandem C(sp(3))–H arylation/[1,2]-Wittig rearrangement of pyridylmethyl ethers is present...
Autores principales: | Gao, Feng, Kim, Byeong-Seon, Walsh, Patrick J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4800319/ https://www.ncbi.nlm.nih.gov/pubmed/27014434 http://dx.doi.org/10.1039/c5sc02739j |
Ejemplares similares
-
Palladium-catalyzed chemoselective direct α-arylation of carbonyl compounds with chloroaryl triflates at the C–Cl site
por: Chen, Zicong, et al.
Publicado: (2022) -
Palladium-catalyzed benzylic C(sp(3))–H carbonylative arylation of azaarylmethyl amines with aryl bromides
por: Zhao, Haoqiang, et al.
Publicado: (2021) -
Carpe diene! Europium-catalyzed [3,3] and [5,5] rearrangements of aryl-pentadienyl ethers
por: Kaiser, Maximilian, et al.
Publicado: (2023) -
How bulky ligands control the chemoselectivity of Pd-catalyzed N-arylation of ammonia
por: Kim, Seoung-Tae, et al.
Publicado: (2019) -
Palladium-catalyzed enantioselective rearrangement of dienyl cyclopropanes
por: Xu, Qi, et al.
Publicado: (2023)