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A nano-organo catalyzed route towards the efficient synthesis of benzo[b]pyran derivatives under ultrasonic irradiation

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TLDR
In this article, an efficient one-pot synthesis of benzo[b]pyrans catalyzed by vitamin B1 functionalized Fe2O3@SiO2 NPs under ultrasonic conditions is reported.
Abstract
An efficient, one-pot synthesis of benzo[b]pyrans catalyzed by vitamin B1 functionalized Fe2O3@SiO2 NPs under ultrasonic conditions is reported herein. The nano-organocatalyst was synthesized and characterized by FT-IR, TEM, EDS, powder XRD, etc. Several benzo[b]pyran derivatives were prepared with satisfactory yields and the nanocatalyst was magnetically retrieved and recycled. The salient features of this protocol include convenient work-up procedure, mild reaction conditions, easy catalyst recovery, shorter reaction time and use of green solvents. Ultrasound energy has been meticulously exploited for the synthesis of a nano-organocatalyst as well as for the preparation of several benzo[b]pyran derivatives. The biological activity of the synthesized benzo[b]pyrans were investigated and one of the derivatives was found to demonstrate profound activity in suppressing the side-effects of chlorpyrifos, an insecticide on the morphology of the external gills of the Duttaphrynus melanostictus tadpoles.

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Journal ArticleDOI

Organocatalysis: A Brief Overview on Its Evolution and Applications

TL;DR: The use of small organic molecules as catalysts has gained increasing importance recently as discussed by the authors, and they present a lot of advantages, like being less toxic, less polluting, and more economically viable than the organometallic catalysts that dominate asymmetric synthesis.
Journal ArticleDOI

A choline chloride-based deep eutectic solvent promoted three-component synthesis of tetrahydrobenzo[b]pyran and pyrano[2,3-d] pyrimidinone (thione) derivatives

TL;DR: An efficient one-pot method for the synthesis of tetrahydrobenzo[b]pyran and pyrano[2,3-d]pyrimidinone (thione) derivatives through a three-component reaction between aldehydes, malononitrile and enolizable C-H activated acidic compounds using a new deep eutectic solvent made of choline chloride, urea and thiourea as an environmentally benign catalyst has been reported.
Journal ArticleDOI

Novel ferrocene substituted benzimidazolium based ionic liquid immobilized on magnetite as an efficient nano-catalyst for the synthesis of pyran derivatives

TL;DR: In this article, a magnetically recoverable Fe3O4@SiO2-BenzIm-Fc[Cl]/NiCl2 nanoparticle was also synthesized using a simple chemical coprecipitation approach.
Journal ArticleDOI

Introduction of an efficient DABCO-based bis-dicationic ionic salt catalyst for the synthesis of arylidenemalononitrile, pyran and polyhydroquinoline derivatives

TL;DR: An affordable bis-dicationic ionic salt ([(DABCO)2C3H5OH]·2Cl) was utilized for the synthesis of arylidenemalononitrile, tetrahydrobenzo[b]pyran, pyrano[2,3-d]-pyrimidinone (thione), dihydropyrano [3,2-c]chromene, and polyhydroquinoline derivatives as mentioned in this paper.
References
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Synthesis and pharmacological activity of 2-oxo-(2H) 1-benzopyran-3-carboxamide derivatives

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