Results 11 to 20 of about 6,457 (248)
Catalytic Cyclization of o‐Alkynyl Phenethylamines via Osmacyclopropene Intermediates: Direct Access to Dopaminergic 3‐Benzazepines [PDF]
NOTICE: This is the peer reviewed version of the following article: Álvarez-Pérez, A., González-Rodríguez, C., García-Yebra, C., Varela, J. A., Oñate, E., Esteruelas, M. A., Saá, C. (2015).
Esteruelas Rodrigo, Miguel Ángel+6 more
core +2 more sources
Inherently complex, lignin-derived aromatic monomers comprising valuable structural moieties present in many pharmaceuticals would serve as ideal substrates for the construction of biologically active molecules.
Saravanakumar Elangovan+6 more
doaj +2 more sources
Iodine(III)-Mediated Oxidation of Anilines to Construct Dibenzazepines. [PDF]
Cyclization: A mild, room temperature oxidative cyclization of 2‐substituted anilines that accesses a broad range of medium‐ring N‐heterocycles via radical intermediates is reported. Abstract The development of an efficient process that produces bioactive medium‐sized N‐heterocyclic scaffolds from 2‐substituted anilines using either iodosobenzene or ...
White CM, Zorigt N, Deng T, Driver TG.
europepmc +2 more sources
Preparation of substituted tetrahydro-1-benzazepines by lithiation-trapping [PDF]
The tetrahydro‐1‐benzazepine or benzo[b]azepine ring system is found in a number of drug molecules although methods to access 2,2‐disubstituted derivatives are rare. Here we report the preparation of N‐tert‐butoxycarbonyl‐2‐phenyltetrahydro‐1‐benzazepine
Aeyad+38 more
core +2 more sources
One-Pot, Water-Mediated, H2O2-HCl Catalyzed Synthesis of Benzazepines
One-pot, multicomponent H2O2-HCl catalyzed system was employed for the synthesis of a series of benzazepine compounds. The implemented procedure oxidized the carbon-nitrogen bonds and produced benzazepines, while integrating diamines and substituted ...
Nidhi Singh, Jaya Pandey
openalex +2 more sources
Review on allosteric modulators of dopamine receptors so far. [PDF]
Abstract Background Contemporary research is predominantly directed towards allosteric modulators, a class of compounds designed to interact with specific sites distinct from the orthosteric site on G protein‐coupled receptors. These allosteric modulators play a pivotal role in influencing diverse pharmacological effects, such as agonism/inverse ...
Girmaw F.
europepmc +2 more sources
Propargyl Amines: Versatile Building Blocks in Post-Ugi Transformations. [PDF]
Applications of propargyl amines in the Ugi reaction and further transformations are discussed in this review. These post‐Ugi transformations, employing transition metal catalysis, base‐mediated reactions and rearrangements, allow the syntheses of diversely substituted scaffolds.
Bhoraniya RB, Modha SG.
europepmc +2 more sources
Heck–Suzuki Tandem Reaction for the Synthesis of 3-Benzazepines [PDF]
A novel procedure for the Heck-Suzuki tandem reaction suitable for the construction of nitrogen-containing medium rings was developed to provide access toward the 3-benzazepine framework.
Anatoly A. Peshkov+5 more
openalex +2 more sources
Convenient Synthesis of 2‐Benzazepines via Radical Cyclization. [PDF]
AbstractFor Abstract see ChemInform Abstract in Full Text.
Akio Kamimura+3 more
openalex +5 more sources
Cycloaddition reactions are among the most practical strategies to assemble cyclic products; however, they usually require the presence of reactive functional groups in the reactants.
Xandro Vidal+2 more
semanticscholar +1 more source