Cargando…
Coordinating activation strategy enables 1,2-alkylamidation of alkynes
The radical 1,2-difunctionalization reaction of alkynes has been evolved into a versatile approach for expeditiously increasing the complexity of the common feedstock alkyne. However, intermolecular 1,2-carboamidation with general alkyl groups is an unsolved problem. Herein, we show that a coordinat...
Autores principales: | Ren, Jing, Xu, Junhua, Kong, Xiangxiang, Li, Jinlong, Li, Kaizhi |
---|---|
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/PMC10599465/ https://www.ncbi.nlm.nih.gov/pubmed/37886104 http://dx.doi.org/10.1039/d3sc03786j |
Ejemplares similares
-
Alkylamides of Acmella oleracea
por: Cheng, Yuan-Bin, et al.
Publicado: (2015) -
Divergent 1,2-carboallylation of terminal alkynes enabled by metallaphotoredox catalysis with switchable triplet energy transfer
por: Qin, Jian, et al.
Publicado: (2023) -
Biocompatible nanocarriers for passive transdermal delivery of insulin based on self-adjusting N-alkylamidated carboxymethyl cellulose polysaccharides
por: Cohen, Yael, et al.
Publicado: (2022) -
Chemistry and Pharmacology of Alkylamides from Natural Origin
por: Elufioye, Taiwo O., et al.
Publicado: (2020) -
Natural Bioactive Cinnamoyltyramine Alkylamides and Co-Metabolites
por: Evidente, Antonio, et al.
Publicado: (2021)