synthesis of open chain analogue of 1,8-dioxooctahydroxanthene catalyzed by aluminosilicate mcm- 41

Synthesis of open chain analogue of 1,8-dioxooctahydroxanthene catalyzed by aluminosilicate MCM- 41

In this study, aluminosilicate MCM-41 has been found to be an efficient catalyst for reaction betweendifferent benzaldehyde derivatives and 5,5-dimethyl-1,3-cyclohexanedione to give open chain analogue of1,8-dioxo-octahydroxanthene in excellent yields. No evidence for the formation of cyclization products wasobserved. The catalyst can be used several times after recovery.

An efficient green synthesis of highly substituted imidazoles catalyzed by Al-MCM-41 nanoreactors

Al-MCM-41 nanoreactors is found to be a remarkable efficient catalyst for one-pot multicomponent cyclocondensation of benzil, aniline or ammonium acetate and aromatic aldehydes for the synthesis of polysubstituted imidazoles under solvent-free conditions. The reaction was efficiently promoted by 10 mg nano-Al-MCM-41 and the heterogeneous catalyst was recycled for four runs in this reaction with...

Hollow spheres of MCM-41 aluminosilicate with pinholes.

Hollow spheres of MCM-41 mesoporous aluminosilicates, with two small holes on the shell, have been synthesized from a surfactant-aluminosilicate gel composite.

Photodecomposition of Water Catalyzed by Zr- and Ti-MCM-41

MCM-41 functionalized sulfonic acid catalyzed one-pot synthesis of 1,8- dioxo-octahydroxanthenes

MCM-41-R-SO3H catalyzed one-pot synthesis of 1,8-dioxo-octahydroxanthenes is reportedunder reflux conditions. The catalyst is easily prepared, highly stable, very simple to handle andrecycled for five times without loss of significant activity

Highly efficient multicomponent Biginelli’s synthesis of 3,4-dihydropyrimidin-2(1H)-ones catalyzed by Al-MCM-41 under solvent-free conditions

In this study, an efficient and green process for the synthesis of dihydropyrimidin-2(1H)-ones from aromatic benzaldehydes, ethyl acetoacetate and urea using Al-MCM-41 as heterogeneous catalyst and microreactor under solvent-free conditions has been developed. The advantages of this method are easy work-up procedure, regeneration of the catalyst, clean and neutral reaction conditions.