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An environmentally friendly, versatile multicomponent reaction for synthesizing isoxazol-5-one and pyrazol-3-one derivatives has been developed, utilizing a freshly prepared g-C3N4·OH nanocomposite as a highly efficient catalyst at room temperature in aqueous environment. This innovative approach yielded all the desired products with exceptionally high yields and concise reaction durations. The catalyst was well characterized by FT-IR, XRD, SEM, EDAX, and TGA/DTA studies. Notably, the catalyst demonstrated outstanding recyclability, maintaining its catalytic efficacy over six consecutive cycles without any loss. The sustainability of this methodology was assessed through various eco-friendly parameters, including E-factor and eco-score, confirming its viability as a green synthetic route in organic chemistry. Additionally, the gram-scale synthesis verifies its potential for industrial applications. The ten synthesized compounds were also analyzed via a PASS online tool to check their several pharmacological activities. The study is complemented by in silico molecular docking, pharmacokinetics, and molecular dynamics simulation studies. These studies discover 5D as a potential candidate for drug development, supported by its favorable drug-like properties, ADMET studies, docking interaction, and stable behavior in the protein binding cavity. [ABSTRACT FROM AUTHOR]

The present work involves an eco-friendly, green, and cost-efficient synthesis of reduced graphene oxide using green extracts of curry leaves and Tulsi seeds as reducing agents. The synthesized reduced GOs (CL-rGO and TS-rGO) were confirmed by XRD, FESEM, EDS, FT-IR, UV-VIS, and TGA studies. The disappearance of the peak at 9.90° and the appearance of a new peak at 2θ = 24.56° and 2θ = 25.62° and a decrease in interlayer spacing from 0.88 nm to 0.34 nm and 0.36 nm in CL-rGO and TS-rGO respectively confirmed the synthesis of reduced GO. The C/O atomic ratio of CL-rGO and TS-rGO was found 4.35 and 4.19 as compared to synthesized GO (C/O atomic ratio 2.65) which confirmed the synthesis of reduced GO. Further, the catalytic applications of synthesized CL-rGO and TS-rGO were studied for the reduction of cinnamaldehyde to cinnamyl alcohol in an aqueous medium yielding 90-91%. Moreover, the degradation of methylene blue and malachite green dyes was studied and found that both dyes were eliminated within 25 and 30 min in dark conditions using CL-rGO and TS-rGO respectively. Both CL-rGO and TS-rGO showed significant antimicrobial activity against different fungal strains but specifically CL-rGO against M. furfur with the minimum inhibitory concentration of 125 µg/mL. Furthermore, CL-rGO and TS-rGO exhibited excellent antimicrobial activity against E. coli with minimum inhibitory concentrations of 62.5 µg/mL and 31.25 µg/mL, respectively. [ABSTRACT FROM AUTHOR]

A highly efficient, green, and multicomponent reaction method has been developed for the diversity‐oriented synthesis of 32 spirooxindole derivatives via the formation of cascade C–N, C–O, and C–S bonds. The synthesis involved starch‐capped zinc oxide nanocomposite as an effective heterogeneous catalyst with the synergistic application of ultrasound and on‐water synthesis. By employing this approach, all desired products were successfully obtained with high yields and comparatively short reaction times. Furthermore, the catalyst employed in the process exhibited excellent recyclability, allowing for its recovery and reuse for up to eight consecutive runs without any loss of catalytic activity. The greenness of the protocol was evaluated by various green metrics such as E‐factor and eco‐score, and the result showed the acceptability of the present method in organic synthesis. [ABSTRACT FROM AUTHOR]

A highly efficient eco-benign pathway was developed for the synthesis of a library of 34 bis(indoyl)methane derivatives using triethylammonium hydrogen sulfate ionic liquid as a green catalyst in high to excellent yields (82–98%) at room temperature. The reaction was easy to execute by simply mixing two equivalents of indole with one equivalent of different aldehydes (including aromatic, heterocyclic, and aliphatic) using ionic liquid as a catalyst and water as a solvent under stirring at mild reaction environment. The current methodology has several benefits such as operational simplicity, short time period (25–60 min), cost-efficient, environment-friendly, easily recoverable catalyst, and highly reusable up to five cycles. [ABSTRACT FROM AUTHOR]

A facile approach for the synthesis of bioactive acridinedione analogs using dimedone, aryl aldehydes, and ammonium acetate was developed using caffeine hydrogen sulfate catalyst in ethanol and water (2:1) solvent mixture at room temperature. The significant advantages of this procedure are efficient and simple method, ambient conditions, short reaction time (5–30 min), simple workup, easily recoverable catalyst, broad substrate scope and good yields (45–80%). Being water soluble, the catalyst was easily recovered by water and reused up to 4 runs. Moreover, the antimicrobial profile of synthesized derivatives was performed against different bacterial and fungal strains using broth microdilution method. Most of the synthesized derivatives exhibited significant activity against bacterial and fungal strains compared to standard. Compounds 4e (31.25 µg/mL and 31.25 µg/mL) and 4g (31.25 µg/mL and 62.5 µg/mL) were found the most active against E. coli. and S. aureus respectively with good MIC values. Compound 4f and 4j displayed the highest antifungal activity against A. niger with31.25 µg/mL MIC value. [ABSTRACT FROM AUTHOR]