Cargando…
Diels–Alder Adducts of Morphinan-6,8-Dienes and Their Transformations †
6,14-ethenomorphinans are semisynthetic opiate derivatives containing an ethylene bridge between positions 6 and 14 in ring-C of the morphine skeleton that imparts a rigid molecular structure. These compounds represent an important family of opioid receptor ligands in which the 6,14-etheno bridged s...
Autores principales: | Marton, János, Fekete, Anikó, Cumming, Paul, Hosztafi, Sándor, Mikecz, Pál, Henriksen, Gjermund |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9102320/ https://www.ncbi.nlm.nih.gov/pubmed/35566212 http://dx.doi.org/10.3390/molecules27092863 |
Ejemplares similares
-
Optimization of a Nucleophilic Two-Step Radiosynthesis of 6-O-(2-[(18)F]fluoroethyl)-6-O-desmethyl-diprenorphine ([(18)F]FE-DPN) for PET Imaging of Brain Opioid Receptors
por: Németh, Enikő, et al.
Publicado: (2023) -
Anionic Diels–Alder Chemistry of Cyclic Sodium
Dien-1-olates Delivering Highly Stereoselective and Functionalized
Polycyclic Adducts
por: Huang, Jing-Kai, et al.
Publicado: (2021) -
Furoic acid and derivatives as atypical dienes in Diels–Alder reactions
por: Cioc, Răzvan C., et al.
Publicado: (2021) -
Diene-modified nucleotides for the Diels–Alder-mediated functional tagging of DNA
por: Borsenberger, Vinciane, et al.
Publicado: (2009) -
Diels–Alder reaction of β-fluoro-β-nitrostyrenes with cyclic dienes
por: Ponomarev, Savva A, et al.
Publicado: (2021)