Results 11 to 20 of about 4,292 (206)

Pharmacological Potential of 3-Benzazepines in NMDAR-Linked Pathophysiological Processes. [PDF]

open access: goldBiomedicines, 2023
The number of N-Methyl-D-aspartate receptor (NMDAR) linked neurodegenerative diseases such as Alzheimer’s disease and dementia is constantly increasing. This is partly due to demographic change and presents new challenges to societies. To date, there are
Ritter N   +4 more
europepmc   +4 more sources

Heck–Suzuki Tandem Reaction for the Synthesis of 3-Benzazepines [PDF]

open access: greenThe Journal of Organic Chemistry, 2015
AbstractThe microwave‐assisted title reaction between N‐protected 2‐(2‐bromoaryl)alkylpropargylamides and organo‐boron compounds gives the corresponding 3‐benzazepin‐2‐ones.
Peshkov, Anatoly A.   +5 more
openaire   +5 more sources

Divergent synthesis of benzazepines and bridged polycycloalkanones via dearomative rearrangement. [PDF]

open access: yesNat Commun, 2022
The dearomative functionalization of aromatic compounds represents a challenging transformation, as it typically needs to overcome a great kinetic barrier.
Shi Q   +10 more
europepmc   +2 more sources

Convenient Synthesis of 2-Benzazepines via Radical Cyclization [PDF]

open access: greenThe Journal of Organic Chemistry, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Masahiko Hagihara   +3 more
openaire   +5 more sources

Carbotrifluoromethylations of C−C Multiple Bonds (Excluding Aryl‐ and Alkynyltrifluoromethylations)

open access: yesChemistry – A European Journal, Volume 29, Issue 19, April 3, 2023., 2023
One main method for the access of organofluorine compounds is the trifluoromethylative functionalization of an olefin bond, which simultaneously introduces a functional group and a trifluoromethyl element into an olefin framework. This review provides a concise overview of this powerful and versatile method. Abstract Organofluorine chemistry has become
Klára Aradi, Loránd Kiss
wiley   +1 more source

Synthesizing Strained Azatriseptane Frameworks

open access: yesHelvetica Chimica Acta, Volume 106, Issue 4, April 2023., 2023
Abstract Embedding seven‐membered rings into polycyclic aromatic molecules is attractive as they can exert an influence on molecular conformation that ultimately changes the solubility and π‐electronics. The considerations in designing and synthesizing a highly strained azatriseptane framework are discussed herein.
Kai Zhang   +3 more
wiley   +1 more source

Palladium-Catalyzed [5+2] Heteroannulation of Phenethylamides with 1,3-Dienes to Dopaminergic 3-Benzazepines [PDF]

open access: yes, 2020
NOTICE: This is the peer reviewed version of the following article: Velasco-Rubio, A., Varela, J. A., Saá, C. (2020). Palladium-Catalyzed [5+2] Heteroannulation of Phenethylamides with 1,3-Dienes to Dopaminergic 3-Benzazepines. Org.
Saá Rodríguez, Carlos   +2 more
core   +1 more source

Ultra‐high‐field pharmacological functional MRI of dopamine D1 receptor‐related interventions in anesthetized rats

open access: yesPharmacology Research &Perspectives, Volume 11, Issue 2, April 2023., 2023
Dopamine D1 receptor manipulation induced BOLD signal changes in anesthetized rat brain which detected using pharmacological functional MRI. D1‐like receptor agonist increased, while the antagonist decreased the BOLD signal intensity in the striatum, thalamus, and cerebellum.
Yuka Kimura   +5 more
wiley   +1 more source

Phenol‐benzoxazolone bioisosteres of GluN2B‐NMDA receptor antagonists: Unexpected rearrangement during reductive alkylation with phenylcyclohexanone

open access: yesArchiv der Pharmazie, Volume 355, Issue 11, November 2022., 2022
To increase the affinity to the N‐methyl‐ d‐aspartate receptors with GluN2B subunit, the phenol of the benzazepine‐based inhibitor WMS‐1410 was replaced bioisosterically by a benzoxazolone moiety and the phenylbutyl side chain was conformationally restricted in a phenylcyclohexyl substituent.
Alexander Markus   +8 more
wiley   +1 more source

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