Herein, the synthesis of graphitic carbon nitride (g-C3N4) via the simple heating of cheap and readily available urea as the starting material has been reported. The catalytic activity of the prepared g-C3N4 was investigated for the synthesis of chromeno[2,3-b]pyridine and benzylpyrazolyl coumarin derivatives in an ethanol medium. The reactions were performed under mild conditions to achieve widely functionalized target products in a one-pot operation. The as-synthesized g-C3N4, being a heterogeneous catalyst, demonstrates excellent recyclability up to the 5th consecutive run without a significant decrease in its catalytic activity and yield of the product. A gram-scale reaction was performed to demonstrate the industrial applications of the present protocol. The green chemistry metrics such as environmental factor (E-factor), atom economy (AE), carbon efficiency (CE), and reaction mass efficiency (RME) were calculated and found to be very close to the ideal values. Additionally, operation simplicity, wide substrate scope, easy reusability of the catalyst, and avoidance of metal contamination in the products drive the process toward green and sustainable development.

In this work, graphite oxide (GO) was developed from cheap and readily available graphite powder and used as a green heterogeneous carbocatalyst towards the synthesis of spirodibenzo[1,4]diazepine derivatives via one-pot...

Herein, palladium containing metal-organic framework was designed for utilizing in C-H functionalization of unactivated arenes. The catalyst was prepared via post-synthetic modification of amino-functionalized MIL-101(Cr) and was well characterized using...

A self-assembly of copper-grafted imidazole polymeric complex is synthesized via a coordinative-convolution method. The structural characterization of the polymeric copper catalyst was completed through FT-IR, SEM, TEM-EDX, SAED, PXRD, TGA,...

A heterogeneous copper-catalyzed A3 coupling reaction of aldehydes, amines, and alkynes for the synthesis of propargylamines and benzofurans has been developed. Here, the modified metal–organic framework MIL-101(Cr)-SB-Cu complex was chosen as the heterogeneous copper catalyst and prepared via post-synthetic modification of amino-functionalized MIL-101(Cr). The structure, morphology, thermal stability, and copper content of the catalyst were determined by FT-IR, PXRD, SEM, TEM, EDX, TGA, XPS, and ICP-OES. The catalyst shows high catalytic activity for the aforementioned reactions under solvent-free reaction conditions. High yields, low catalyst loading, easy catalyst recovery and reusability with not much shrink in catalytic activity, and a good yield of 82% in gram-scale synthesis are some of the benefits of this protocol that drove it towards sustainability.