In this research, magnetic Fe 3 O 4 -NP nanoparticles were synthesized employing a green biosynthetic procedure by reduction of ferric chloride solution with clover leaf water extract. The nanoparticles prepared via this biosynthesis method can potentially be valuable for different purposes such as organic synthesis. In this research, 1,3-benzoxazole derivatives were generated via a multicomponent reaction of α-bromo ketones, isothiocyanate, and propiolate in the presence of a catalytic amount of bio-Fe 3 O 4 MNPs and sodium hydride in water at 50 C in good yields. The catalyst was reused five times with a minor decrease in its catalytic activity. K E Y W O R D S 1,3-benzoxazole, alkyl (aryl) isothiocyanates, clover leaf, Fe 3 O 4 MNPs, isothiocyanates

A series of tetrahydrobenzo [c]acridinone derivatives have been prepared by a one-pot fourcomponent reaction of 1-naphthol, aromatic aldehydes, dimedone, and ammonium acetate in aqueous media using a catalytic amount of titanium dioxide nanoparticles (TiO 2 NPs). The advantages of this novel protocol include the excellent yields, operational simplicity, short reaction time, easy work-up, reusability of the catalyst and an environmentally friendly procedure.

We report on the preparation of a series of 2,4-diamino-6-aryl-5-pyrimidinecarbonitriles, a new efficient protocol, via the condensation reaction of aromatic aldehydes, malononitrile, and guanidine nitrate using a TiO2–SiO2 nanocomposite with a molar ratio of 1:1 as a heterogeneous catalyst. The use of a low-cost and reusable catalyst under mild and solvent-free conditions, and simplicity in operation with easier isolation of the products in high to excellent yields are the main advantages of this highly versatile and eco-friendly protocol.

In this research, green procedure was employed for biosynthesis of magnetic nanoparticles of iron oxide (Fe3O4‐MNPs) by reduction of ferric chloride solution with Orange peel water extract. Also, dihydro‐2H‐cyclopenta[d][1,3]oxazole was generated through multicomponent reaction of 1,3‐oxazole‐2(3H)‐thione, dialkyl acetylenedicarboxylates, α‐haloketones, and Fe3O4‐MNPs as catalyst at ambient temperature in good yield. Initially, 1,3‐oxazole‐2(3H)‐thione derivatives as one of the precursors are produced through the reaction of alkyl bromides, isothiocyanate, sodium hydride, and Fe3O4‐MNPs as catalyst water at ambient temperature in 83–95% yields. Also, diphenyl‐picrylhydrazine radical trapping and ferric reduction activity potential assays are used for evaluation of antioxidant activity of some synthesized compounds. Among investigated compounds, 4b has good power for radical trapping activity and 4d has good reduction power to butylated hydroxytoluene and 2‐tert‐butylhydroquinone.

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