Cargando…
Substrate-Controlled Diversity-Oriented Synthesis of Novel Polycyclic Frameworks via [4 + 2] and [3 + 2] Annulations of Ninhydrin-Derived MBH Adducts with 3,4-Dihydroisoquinolines
Substrate-controlled diversity-oriented synthesis of polycyclic frameworks via [4 + 2] and [3 + 2] annulations between ninhydrin-derived Morita–Baylis–Hillman (MBH) adducts and 3,4-dihydroisoquinolines under similar reaction conditions have been developed. The reaction provides diversity-oriented sy...
Autores principales: | Wang, Kaikai, Zhou, Wenwen, Jia, Jun, Ye, Junwei, Yuan, Mengxin, Yang, Jie, Qi, Yonghua, Chen, Rongxiang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10574269/ https://www.ncbi.nlm.nih.gov/pubmed/37836604 http://dx.doi.org/10.3390/molecules28196761 |
Ejemplares similares
-
Facile Synthesis of Tricyclic 1,2,4-Oxadiazolines-Fused Tetrahydro-Isoquinolines from Oxime Chlorides with 3,4-Dihydroisoquinoline Imines
por: Wang, Kaikai, et al.
Publicado: (2022) -
Rh(iii)-catalyzed synthesis of tetracyclic isoquinolinium salts via C–H activation and [4+2] annulation of 1-phenyl-3,4-dihydroisoquinolines and alkynes in ethanol
por: Dang, Xinxin, et al.
Publicado: (2018) -
In Silico Screening for Novel Leucine Aminopeptidase Inhibitors with 3,4-Dihydroisoquinoline Scaffold
por: Ziemska, Joanna, et al.
Publicado: (2020) -
N-Aryl-3,4-dihydroisoquinoline
Carbothioamide Analogues as Potential Urease Inhibitors
por: Ali, Fayaz, et al.
Publicado: (2021) -
Design, Synthesis and Biological Evaluation of 1,4-Disubstituted-3,4-dihydroisoquinoline Compounds as New Tubulin Polymerization Inhibitors
por: Zhang, Ling, et al.
Publicado: (2015)