In this study, solvent-free and phase transfer catalysis conditions coupled with microwave irradiation and their advantages in synthesis of N-alkylation of primary anilines were reported. In this way two different microwave processing techniques were compared in terms of reaction yields. Consequently, microwave irradiation significantly reduced reaction times compared to traditional heating met...

dodecylbenzenesulfonic acid (dbsa) was used as an efficient, cheap and stable brønsted catalyst for acetylation of alcohols and phenols and formylation of alcohols under solvent-free conditions. various primary, secondary and tertiary alcohols were acetylated with acetic anhydride as an acetylating agent under solvent-free conditions in the presence of catalytic amount of dbsa at room temperatu...

the aim of this research is to study ni2+ supported on hydroxyapatite-core-shell magnetic γ-fe2o3 nanoparticles (γ-fe2o3@hap-ni2+) as a green and recyclable catalyst for the biginelli reaction under solvent-free conditions. one-pot multi-component condensation of 1,3-dicarbonyl compounds, urea and aldehydes at 80 oc affords the corresponding compounds in high yields and in short reaction times ...

an improved, simple, and facile synthesis of 3,4-dihydropyrimidin-2(1h)-ones by employing three-component, one-pot condensation reaction of β-keto ester, aromatic aldehydes, and urea or n-methylurea using lacl3/clch2cooh as an inexpensive and green chemistry catalyst system under solvent-free conditions described. compared with the classicalbiginelli reaction conditions, this method has the adv...

oxidation of some benzoins to benziles is reported by using p-toluenesulfonic acid as aselective oxidation catalyst under solvent-free condition in high yield. the adjacent carbonylgroup is necessary for the oxidation of hydroxyl group in these compounds. the reaction iscarried out in a sand-bath at 100 °c with minimum by-products.

derivatives of thiazolidinone ring systems are known to act as anti-hiv infections , analgesic, anti-bacterial, anti-convulsant, anti parasitic, potential anti-inflammatory and herbicidal agents. due biological activities of thiazolidinones ring, several methods for their synthesis have been illustrated in literature. imidazolidine-2-thiones were synthesized by the oxidative cyclization of 1-be...

a series of tri- and tetra- substituted imidazoles were synthesized from benzyl, aldehyde and ammonium acetate in the presence of zeolite as an ecofriendly reusable catalyst under microwave irradiation in the absence of solvent. the yields are high to excellent and the use of microwave irradiation reduces reaction times to few minute.

Reaction coordinates for chemical reactions in solution are often of a collective nature involving solvent degrees of freedom. A recent generalization of the blue-moon ensemble technique has enabled us to determine the free energy required to change these variables, using them as constraints in a molecular dynamics simulation. We discuss a Ðrst application to the free energy of coordination Ñuc...

a  convenient  and  efficient  one-pot  four-component  synthesis  of  1,  2,  4,  5-tetrasubstituted  imidazoles  using  nano  tio2  as  a  recyclable  catalyst  is  reported.  the results  show  that  the  methodology  has  several  advantages  such  as  low  loading  of catalyst,  excellent  yield,  short  reaction  time,  operational  simplicity  and  solvent-free conditions.

a rapid and efficient one-pot, four-component protocol towards the synthesis of polyhydroquinoline derivatives has been developed. the condensation of aldehyde, dimedone, ethyl acetoacetate and ammonium acetate in presence of stannous chloride was carried out under solvent free condition to synthesize a variety of polyhydroquinoline derivatives in good to excellent yields. stannous chloride was...