Synthesis and evaluation of antimicrobial and antioxidant activity of novel 7-Aryl-6H,7H- benzo[f]chromeno[4,3-b]chromen-6-one by MgO nanoparticle as green catalyst

Using MgO nanoparticle as a recyclable and efficient catalyst, multicomponent reaction of 2-Naphthol, aldehyde derivatives, 4-hydroxycoumarin has led to the synthesis of novel 7-Aryl-6H,7H- benzo[f]chromeno[4,3-b]chromen-6-one derivatives. This study aimed to examine the antimicrobial and antioxidant effects of the synthetic compound in order to reach some benefits, including the synthesis of new derivatives with biological properties, shorter time, high yields, and concordance with green chemistry.     

γ‐Spiroiminolactone Synthesis by Reaction of Acetylenic Esters and α‐Dicarbonyl Compounds in the Presence of Aryl Isocyanide

The highly reactive 1∶1 intermediate produced in the reaction of aryl isocyanides and acetylenic esters was trapped by the α‐dicarbonyl compounds to yield γ‐spiroiminolactone derivatives in good yields.     

Reaction of Alkyl and Aryl Isocyanides with Floren‐9‐ones in the Presence of Acetylenic Esters: Preparation of γ‐Spiroiminolactones

The reactive 1∶1 intermediate generated by the addition of alkyl and aryl isocyanides to dialkyl acetylenedicarboxylate was trapped by 2,7‐dinitrofloren‐9‐one and floren‐9‐one to yield iminolactones in good yields.     

One-Pot Synthesis of Stable Phosphorus Ylides Using CH-Acid Compounds

Stable crystalline phosphorus ylides were obtained in excellent yields from the 1:1:1 addition reaction between triphenylphosphine and di-tert-butyl acetylendicarboxylate, in the presence of antron, dimedone, indandion, and 3,5-dimethylbarbituric acid. These stable ylides exist in a solution as a mixture of two geometrical isomers as a result of restricted rotation around the carbon-carbon partial double bond resulting from conjugation of the ylide moiety with the adjacent carbonyl group.     

A Novel and Efficient Synthesis of α-Aminophosphonates by Use of Triphenyl Phosphite in Acetic Acid Media

Abstract

For the first time, α-aminophosphonates were obtained by a simple and efficient one-pot method from the reaction between aldehyde, aniline, and triphenyl phosphite in the presence of acetic acid as a catalyst and solvent at room temperature.

Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file.

GRAPHICAL ABSTRACT     

Synthesis and characterization of Fe3O4@THAM-SO3H as a highly reusable nanocatalyst and its application for the synthesis of dihydropyrano[2,3-c]pyrazole derivatives

In this work, a new, green and beneficial nanomagnetic catalyst was easily fabricated using sulfuric acid as an acidic group on Fe₃O₄ nanoparticles coated with tris (hydroxymethyl) aminomethane (THAM). The synthesized catalyst was characterized by FT-IR, TGA/DTG, XRD, TEM, EDS, VSM, and SEM analyses. Next, its catalytic activity was studied for the synthesis of dihydropyrano[2,3-c]pyrazole derivatives. This catalyst has advantages such as high catalytic activity, non-toxicity, easy separation from the reaction mixture using an external magnet and reuses for several times without significantly reducing in its catalytic activity.     

An efficient method for synthesis of stable phosphorus ylides and 1,4-diionic organophosphorus compounds in the presence of sodium dodecyl sulfate in aqueous media

Stable crystalline phosphorus ylides and 1,4-diionic organophosphorus compounds were obtained in good to excellent yields from the 1:1:1 addition reaction between triphenylphosphine, dialkyl acetylenedicarboxylates and β-dicarbonyl or heterocyclic compounds, such as diethyl malonate, acetyl acetone, 1,3-diphenyl propane-1,3-dione, 1,3-dimethylbarbituric acid, meldrum’s acid, 2-benzoxazolinone, benzotirazole, and 2-thiazoline-2-thiol in the presence of sodium dodecyl sulfate as a surfactant in water. Green synthesis, mild conditions, decreasing timescale of reaction, low cost, and easy workup are the main advantages of this method.     

An efficient synthesis of α‐Amino phosphonates using silica sulfuric acid as a heterogeneous catalyst

α‐Amino phosphonates were obtained in a one‐pot, simple, and efficient method from the reaction between aldehyde, aniline, trialkyl phosphite, and silica sulfuric acid as a catalyst in acetonitrile at room temperature. © 2009 Wiley Periodicals, Inc. Heteroatom Chem 20:316–318, 2009; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/hc.20543