2013
DOI: 10.1016/j.molcata.2013.03.017
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Simultaneously application of SBA-15 sulfonic acid nanoreactor and ultrasonic irradiation as a very useful novel combined catalytic system: An ultra-fast, selective, reusable and waste-free green approach

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Cited by 62 publications
(25 citation statements)
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“…Interestingly, it was observed that the catalytic activity and selectivity for IRMOF-3 were higher than that for porous SBA-15/SO 3 H, which gave rise to a mixture of a-aminophosphonate and a-hydroxyphosphonate. [81] 4.13. Condensation/olefin hydrogenation/nitro reduction The potential of MOFs as multifunctional catalyst stems from the possibility to contain simultaneously orthogonal or even antagonistic active sites either at the metal nodes, organic linkers, or empty space.…”
Section: Condensation/additionmentioning
confidence: 99%
“…Interestingly, it was observed that the catalytic activity and selectivity for IRMOF-3 were higher than that for porous SBA-15/SO 3 H, which gave rise to a mixture of a-aminophosphonate and a-hydroxyphosphonate. [81] 4.13. Condensation/olefin hydrogenation/nitro reduction The potential of MOFs as multifunctional catalyst stems from the possibility to contain simultaneously orthogonal or even antagonistic active sites either at the metal nodes, organic linkers, or empty space.…”
Section: Condensation/additionmentioning
confidence: 99%
“…[220]. [224]. The synthesis of these products has been also achieved by a similar procedure using SBA-Pr-SO 3 H under solvent-free conditions [225].…”
Section: Application Of Sba-pr-so 3 H In Three-component Reactionsmentioning
confidence: 99%
“…Replacing dimedone with malononitrile or ethyl cyanoacetate in this reaction was also investigated [226]. The effectiveness of combined ultrasound/nanoreactor catalytically system as an ultra-fast, waste-free and highly reusable method for the generation of α-aminophosphonates 132 via a three-component coupling has been also explored (Scheme 44) [224].…”
Section: Application Of Sba-pr-so 3 H In Three-component Reactionsmentioning
confidence: 99%
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“…1 [19]. Due to the above listed excellent therapeutic applications of the 1,4-dihydropyridine derivatives, synthetic chemists have explored several protocols for the synthesis of them using different reaction conditions and varied catalytic systems as follows: Yb(OTf) 3 [20], [pyridine-SO 3 H]Cl [21], [Dsim]HSO 4 [22], Triton X-100 in water [23], TiO 2 NPs [24], SnO 2 NPs [25], silica-bonded imidazolium-sulfonic acid chloride [26], [2-MPyH]OTf [27], SBA-15/SO 3 H [28], Ninanoparticles [29], IL-HSO 4 @SBA-15 [30], Baker's yeast [31], Lproline [32], and [bmim]BF 4 [33]. Although the reported methods offer several merits and provide improvements for the synthesis of the target molecules, many of these protocols need longer reaction times, hard reaction conditions, using unsafe organic solvents, and drastic workups.…”
Section: Introductionmentioning
confidence: 99%