Cargando…
Highly Selective Cyclization and Isomerization of Propargylamines to Access Functionalized Quinolines and 1-Azadienes
Developing new organic reactions with excellent atom economy and high selectivity is significant and urgent. Herein, by ingeniously regulating the reaction conditions, highly selective transformations of propargylamines have been successfully implemented. The palladium-catalyzed cyclization of propa...
Autores principales: | Wu, Zheng-Guang, Zhang, Hui, Cao, Chenhui, Lu, Chaowu, Jiang, Aiwei, He, Jie, Zhao, Qin, Tang, Yanfeng |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10488633/ https://www.ncbi.nlm.nih.gov/pubmed/37687088 http://dx.doi.org/10.3390/molecules28176259 |
Ejemplares similares
-
A low-nuclear Ag(4) nanocluster as a customized catalyst for the cyclization of propargylamine with CO(2)
por: Li, Lin, et al.
Publicado: (2023) -
Solvent-free synthesis of propargylamines: an overview
por: Manujyothi, Ravi, et al.
Publicado: (2021) -
The Asymmetric A(3)(Aldehyde–Alkyne–Amine) Coupling: Highly Enantioselective Access to Propargylamines
por: Mo, Jia-Nan, et al.
Publicado: (2019) -
Intramolecular Cyclization During Bromination of the Quinoline Alkaloid Haplophyllidine
por: Ubaidullaev, A. U., et al.
Publicado: (2022) -
Thiazine-2-thiones as Masked 1-Azadienes in Cascade Dimerization Reactions
por: Kruithof, Art, et al.
Publicado: (2017)