Results 11 to 20 of about 10,026 (250)
© 2014 American Chemical Society. 3,4,6-Tri-O-acetyl-d-galactal is selectively converted into 1-O-aryl-2-deoxy derivatives or chiral bridged benzopyrans under Al(OTf)3 catalysis, depending on reaction conditions.
Sandile B. Simelane +3 more
semanticscholar +2 more sources
Antifeedant Activity of Benzopyrans from Melicope latifolia [PDF]
Two benzopyrans, evodionol (1), and evodion (2) were isolated from the stem bark of Melicope latifolia. The structure of both compounds was identified based on 1D and 2D NMR, UV, and IR spectroscopy.
Tanjung, Mulyadi
core +1 more source
Background New agents for developing alternative or complementary medicine to treat the hepatitis C virus (HCV) are still needed due to high rates of HCV infection globally and the current limitations of available treatments.
Aty Widyawaruyanti +9 more
doaj +1 more source
In current work, a magnesium oxide nanocatalyst was synthesized via greener route using aloe-vera plant leaf extracts as a reducing and stabilizing agent to construct MgO nanoparticle.
Har Lal Singh +4 more
doaj +1 more source
An overview of structure-based activity outcomes of pyran derivatives against Alzheimer’s disease
Pyran is a heterocyclic group containing oxygen that possesses a variety of pharmacological effects. Pyran is also one of the most prevalent structural subunits in natural products, such as xanthones, coumarins, flavonoids, benzopyrans, etc. Additionally
Faisal A. Almalki
doaj +1 more source
σ1 and/or σ2 receptors play a crucial role in pathological conditions such as pain, neurodegenerative disorders, and cancer. A set of spirocyclic cyclohexanes with diverse O-heterocycles and amino moieties (general structure III) was prepared and ...
Elisabeth Kronenberg +8 more
semanticscholar +1 more source
Synthesis of novel photochromic pyrans via palladium-mediated reactions
Photochromic pyrans for applications in material and life sciences were synthesized via palladium-mediated cyanation, carbonylation and Sonogashira cross-coupling starting from bromo-substituted naphthopyran 1 and benzopyrans 2a/b.
Christoph Böttcher +7 more
doaj +1 more source
On the basis of the finding that various aminoalkyl-substituted chromene and chromane derivatives possess strong and highly selective in vitro bioactivity against Plasmodium falciparum, the pathogen responsible for tropical malaria, we performed a ...
Friederike M. Wunsch +3 more
doaj +1 more source
Tricyclic flavonoids with 1,3-dithiolium substructure
The synthesis of new 3-dithiocarbamic flavonoids has been accomplished by the reaction of the corresponding 2-hydroxyaryl dithiocarbamates with aminals. These flavonoids were obtained as a mixture of diastereoisomers, the anti isomer being the major one.
Lucian G. Bahrin +2 more
doaj +1 more source
Successive rounds of chemical modification in three generations of benzopyran molecules have shown to select for different mechanisms of actions and progressive increases in anti-cancer activity.
Alexander J. Stevenson +6 more
semanticscholar +1 more source

