Pd nanoparticles supported on Fe3O4@SiO2-Schiff base as an efficient magnetically recoverable nanocatalyst for Suzuki–Miyaura coupling reaction

Research on Chemical Intermediates - In this work, Pd nanoparticles (Pd-NPs) were decorated on modified magnetic nanoparticles (MNPs) and used as an efficient and recyclable catalyst for the Suzuki...     

Assessment of WENO schemes for multi‐dimensional Euler equations using GPU

This paper presents a detailed study on the implementation of Weighted Essentially Non‐Oscillatory (WENO) schemes on GPU. GPU implementation of up to ninth‐order accurate WENO schemes for the multi‐dimensional Euler equations of gas dynamics is presented. The implementation detail is discussed in the paper. The computational times of different schemes are obtained and the speedups are reported for different number of grid points. Furthermore, the execution times for the main kernels of the code are given and compared with each other. The numerical experiments show the speedups for the WENO schemes are very promising especially for fine grids. Copyright © 2014 John Wiley & Sons, Ltd.     

Ru(II) complexes bearing tertiary phosphine ligands: a novel and efficient homogeneous catalyst for one‐pot synthesis of dihydropyrano[3,2‐c]chromene and tetrahydrobenzo[b]pyran derivatives

A number of ruthenium complexes were prepared and their catalytic activities in three‐component one‐pot condensation of aldehydes, malononitrile and 4‐hydroxycoumarin or dimedone was considered to afford dihydropyrano[3,2‐c]chromenes and tetrahydrobenzo[b]pyran derivatives under optimum reaction conditions. We found that a catalytic amount of RuBr₂(PPh₃)₄ efficiently promotes the reaction in a short time (3–15 min) and with high yield (75–88%). Copyright © 2012 John Wiley & Sons, Ltd.     

One‐Pot Synthesis and Characterization of Some New Types of 5,5′‐Disubstituted Bis(imidazolidine‐2,4‐diones)

The synthesis and structural elucidation of some novel 5,5′‐disubstituted spiro and nonspiro‐bis‐hydantoins are reported. The Bucherer Burge's method has been modified for the preparation of some 5,5′‐substituted bis(imidazolidine‐2,4‐dione) derivatives starting with diketones ( 1–5 ) and dialdehydes ( 6 , 7 ). In some cases, diastereoisomeric mixtures of compounds were obtained. The resulting bis‐hydantoins ( 8–11 , 13 , 14 ) have not to our knowledge been previously reported in the literature.     

Epoxidation of 1,4-Diaroyl Ethene Derivatives in the Presence of UHP or H2O2

Hydrogen peroxide (H₂O₂) or urea–hydrogen peroxide (UHP) in basic media react with carbon–carbon double bonds of 1,4-diaroyl ethenes to produce the corresponding epoxides.     

Dianion-Based Methodology for the Preparation of 2,3-Disubstitutrd Butyrolactones

Unsymmetricai coupling utilizing the reaction of acylsulfonamide dianions with alpha-iodocarboxylate salts followed by a sequence consisting of selective reduction of the carboxylic acid group, hydrolysis of the acylsulfonamide, and spontaneous ring closure affords 2,3-disubstituted butyrolactones.     

A green and practical method for the synthesis of novel pyrano[2,3-<Emphasis Type="Italic">c</Emphasis>]pyrazoles and <Emphasis Type="Italic">bis</Emphasis>-pyrano[2,3-<Emphasis Type="Italic">c</Emphasis>]pyrazoles using sulfonic acid-functionalized ionic liquid

An efficient and practical protocol was developed for the synthesis of novel pyrano[2,3-c]pyrazoles and bis-pyrano[2,3-c]pyrazoles by one-pot four-component reaction of arylaldehyde, ethyl acetoacetate, hydrazine hydrate and dimethyl malonate using SO₃H-functionalized ionic liquid [DMBSI]HSO₄ as a potential green catalyst under solvent-free condition. The method presented is mild, environmentally friendly, inexpensive and functionality tolerant and produces the desired pyranopyrazoles in short reaction times (17–24 min) and excellent yields (85–95%). In addition, the catalyst can be reused at least ten times without almost any change in its catalytic activity.