Chalcones as Versatile Synthons for the Synthesis of 5-and 6-membered Nitrogen Heterocycles
H MT Albuquerque, C MM Santos… - Current Organic …, 2014 - ingentaconnect.com
Chalcones belong to the flavonoid family which constitutes one of the major classes of
naturally occurring oxygen heterocyclic compounds. The α, β-unsaturated carbonyl system …
naturally occurring oxygen heterocyclic compounds. The α, β-unsaturated carbonyl system …
One-pot and two-pot synthesis of chalcone based mono and bis-pyrazolines
Pyrazoline is an important heterocyclic compound in organic and pharmaceutical industry.
The pyrazoline-based compounds are intensively used in medicines and agricultural …
The pyrazoline-based compounds are intensively used in medicines and agricultural …
[HTML][HTML] Synthesis, characterization and antimicrobial activity of peanut skin extract-azo-compounds
Peanut skin extract, an agro-waste and a source of flavonoids has been extracted from
peanut skin and employed as a precursor for the synthesis of novel azo compounds and …
peanut skin and employed as a precursor for the synthesis of novel azo compounds and …
Synthesis, characterization, antioxidant power and acute toxicity of some new azo-benzamide and azo-imidazolone derivatives with in vivo and in vitro antimicrobial …
In this research paper, a stepwise chemical reaction was conducted to synthesize and
develop of a new potent azo-oxazolone, which was used as prototypical molecule for …
develop of a new potent azo-oxazolone, which was used as prototypical molecule for …
Synthesis, spectroscopic and computational characterization of the tautomerism of pyrazoline derivatives from chalcones
FB Miguel, JA Dantas, S Amorim, GFS Andrade… - … Acta Part A: Molecular …, 2016 - Elsevier
In the present study a series of novel pyrazolines derivatives has been synthesized, and
their structures assigned on the basis of FT-Raman, 1 H and 13 C NMR spectral data and …
their structures assigned on the basis of FT-Raman, 1 H and 13 C NMR spectral data and …
One-pot three-component synthesis of some new azo-pyrazoline derivatives
The starting material azo-benzyloxy acetophenone (2) has been synthesized in three steps;
the direct diazotization of p-aminoacetophenone and its coupling reaction with m-cresol …
the direct diazotization of p-aminoacetophenone and its coupling reaction with m-cresol …
Drying and adhesive properties of novel surface coatings derived from peanut skin extract and cashew nutshell liquid
Purpose This study aims to synthesize pigment and resin from agro-wastes and use them in
the formulation of eco-friendly surface coatings. Design/methodology/approach The …
the formulation of eco-friendly surface coatings. Design/methodology/approach The …
Design, Synthesis and Molecular Docking Studies of Novel Thiadiazole Analogues with Potential Antimicrobial and Anti-inflammatory Activities
Background: Chemical modification of thiadiazole may lead to a potent therapeutic agent. In
this study, biological properties of thiadiazole derivatives were evaluated by assessing their …
this study, biological properties of thiadiazole derivatives were evaluated by assessing their …
[PDF][PDF] Synthesis, characterization and testing of biological activity of some novel chalcones derivatives of coumarin
HA DESHPANDE, HN CHOPDE… - Chemical Science …, 2013 - e-journals.in
In the present communication, we herein report the synthesis of some novel derivatives of
coumarin ie. 3-((2E)-(3-(2-hydroxy-5-((aryl) diazenyl) phenyl) acryloyl)-2H-chromen-2-one …
coumarin ie. 3-((2E)-(3-(2-hydroxy-5-((aryl) diazenyl) phenyl) acryloyl)-2H-chromen-2-one …
Exploring Biological Interactions: A New Pyrazoline as a Versatile Fluorescent Probe for Energy Transfer and Cell Staining Applications
BM Beşer, B Yildirim - ChemistryOpen, 2023 - Wiley Online Library
Fluorescent dyes are used in biological systems, because they are highly sensitive and
selective. In this work, we investigated the fluorescent probe properties of 2‐(5‐(pyridin‐2 …
selective. In this work, we investigated the fluorescent probe properties of 2‐(5‐(pyridin‐2 …