N-Heterocyclic carbene catalysed 1, 6-hydrophosphonylation of p-quinone methides and fuchsones: an atom economical route to unsymmetrical diaryl-and …

P Arde, RV Anand - Organic & Biomolecular Chemistry, 2016 - pubs.rsc.org
A convenient organocatalytic approach to access unsymmetrical diaryl-and triarylmethyl
phosphonates using NHC as a Brønsted base catalyst is described. This atom-economical …

[PDF][PDF] Click synthesis, anticancer activity, and molecular docking investigation of some functional 1, 2, 3-triazole derivatives

M Hrimla, A Oubella, Y Laamari, L Bahsis… - Biointerface Res. Appl …, 2022 - roderic.uv.es
Abstract: 1, 2, 3-triazole skeleton is a privileged building block for the discovery of new
promising anticancer agents. In this report, new 1, 4-disubstituted 1, 2, 3-triazoles with the …

Supported CuBr on graphene oxide/Fe 3 O 4: A highly efficient, magnetically separable catalyst for the multi-gram scale synthesis of 1, 2, 3-triazoles

X Xiong, H Chen, Z Tang, Y Jiang - RSC Advances, 2014 - pubs.rsc.org
A superparamagnetic graphene oxide (GO)/Fe3O4–CuBr catalyst was prepared via a simple
chemical method and characterized by Fourier transform infrared (FTIR), thermal gravimetric …

Design and synthesis of nanorods Fe3O4@ S-TiO2/Cu as a green, and regioselective nanocatalyst in the synthesis of 1, 4–disubstituted–1, 2, 3–triazoles

N Moeini-Eghbali, H Eshghi - Inorganic Chemistry Communications, 2023 - Elsevier
A new and regioselective nanocatalyst (Fe 3 O 4@ S-TiO 2/Cu) was synthesized by the
solvothermal method. In this research, sulfur heteroatoms were doped on Fe 3 O 4@ TiO 2 …

Design, synthesis and antiproliferative activity of functionalized flavone-triazole-tetrahydropyran conjugates against human cancer cell lines

N Ahmed, NK Konduru, S Ahmad, M Owais - European Journal of …, 2014 - Elsevier
Under optimized reaction conditions, an efficient synthetic method has been developed to
afford the functionalized flavone-triazole-tetrahydropyran conjugates via click reactions. The …

NHC catalysed trimethylsilylation of terminal alkynes and indoles with Ruppert's reagent under solvent free conditions

P Arde, V Reddy, RV Anand - RSC Advances, 2014 - pubs.rsc.org
An organo-catalytic protocol for the trimethylsilylation of terminal alkynes employing
Ruppert's reagent (CF3SiMe3) as a trimethylsilyl source has been developed under solvent …

N-Heterocyclic carbene catalyzed regioselective oxo-acyloxylation of alkenes with aromatic aldehydes: a high yield synthesis of α-acyloxy ketones and esters

RN Reddi, PV Malekar, A Sudalai - Organic & Biomolecular Chemistry, 2013 - pubs.rsc.org
An N-heterocyclic carbene (NHC)-catalyzed reaction of alkenes with aromatic aldehydes
providing for a high yield synthesis of α-acyloxy ketones and esters has been described …

Visible Light-Promoted Oxidative Cross-Coupling of Alcohols to Esters

A Dellisanti, E Chessa, A Porcheddu, M Carraro… - Molecules, 2024 - mdpi.com
Ester is one of the most significant functional groups in organic chemistry and is enclosed in
several valued molecules. Usually, esters are prepared through the acid-catalyzed …

[3+2]‐Cycloaddition Reactions of gem‐Difluorocyclopropenes with Azomethine Ylides – Access to Novel Fluorinated Scaffolds

K Donnelly, A Singh, T Tuttle… - Chemistry–A European …, 2023 - Wiley Online Library
The introduction of fluorinated moieties into drugs as well as the increase of their overall
three‐dimensionality have become key strategies amongst medicinal chemists to generate …

Silver-catalysed azide–alkyne cycloaddition (AgAAC): assessing the mechanism by density functional theory calculations

B Banerji, K Chandrasekhar, SK Killi… - Royal Society …, 2016 - royalsocietypublishing.org
'Click reactions' are the copper catalysed dipolar cycloaddition reaction of azides and
alkynes to incorporate nitrogens into a cyclic hydrocarbon scaffold forming a triazole ring …