A three-component reaction between 1,2-phenylenediamine, ferrocenecarbaldehyde, and isocyanides in the presence of a catalytic amount of p-toluenesulfonic acid for the synthesis of 3,4-dihydroquinoxalin-2-amine derivatives containing a ferrocene unit is reported. This approach is an effective procedure because the products have a broad spectrum of biological and pharmacological activities such ...

in the current study, a magnetic inorganic–organic nanohybrid material (hpa/tpi-fe3o4) was produced and used as an efficient, highly recyclable and eco-friendly catalyst for the one-pot and multicomponent synthesis of 3,4-dihydroquinoxalin-2-amine, diazepine-tetrazole and benzodiazepine-2-carboxamide derivatives with high yields and in a short range of time (20–35 min). the nanohybrid catalyst ...

3-Acylmethylidene-3,4-dihydroquinoxalin-2(1H)-ones are compounds which possess a wide range of physical and pharmaceutical applications. These compounds can be easily prepared by cyclocondensation of o-phenylenediamines and aroylpyruvates. Unsymmetrically substituted o-phenylenediamines can be obtained form regioisomeric mixtures of 3,4-dihydroquinoxalin-2(1H)-ones. It is often quite difficult ...

In the current study, a magnetic inorganic–organic nanohybrid material (HPA/TPI-Fe3O4) was produced and used as an efficient, highly recyclable and eco-friendly catalyst for the one-pot and multicomponent synthesis of 3,4-dihydroquinoxalin-2-amine, diazepine-tetrazole and benzodiazepine-2-carboxamide derivatives with high yields and in a short range of time (20–35 min)...

The inhibition potential of four Quinoxaline derivatives namely 1,4-dihydroquinoxaline-2,3dione, (3E)-3-hydrazinylidene-3,4-dihydroquinoxalin-2(1H)-one, 1-[(2E)-3-oxo-3,4dihydroquinoxalin-2(1H)-ylidene]urea and 1-[(2E)-3-oxo-3,4-dihydroquinoxalin-2(1H)ylidene]thiourea have been investigated against mild steel in 1M H2SO4 solution using conventional weight loss, electrochemical impedance spectro...

A visible-light photoredox functionalization of 3,4-dihydro-quinoxalin-2-ones with pyrazolones using an inexpensive organophotoredox catalyst is described. The reaction uses 9,10-phenanthrenedione as photocatalyst, a very simple and cheap HP single Blue LED (455 nm) source oxygen from air terminal oxidant, obtaining the corresponding acetylated pyrazoles good yields. can be extended to other ni...

Abstract Financial support from grant PID2020‐116944GB funded by MCIN/AEI/10.13039/501100011033 and “ERDF A way of making Europe” CIAICO/2021/147 Conselleria d'Innovació, Universitat, Ciència i Societat Digital is acknowledged. J.R.‐B. thanks the Ministerio de Ciencia, Innovación y Universidades for a FPU predoctoral contract (FPU17/00688). C.V. RyC (RYC‐2016‐20187) “European Union NextGenerati...