Vitamin B1 supported on silica-encapsulated γ-Fe2O3 nanoparticles: design, characterization and application as a greener biocatalyst for highly efficient acylation
“…Recently, the Azizi and Heydari reported acylation of phenols and alcohols using vitamin B 1 supported on silica-encapsulated γ-Fe 2 O 3 nanoparticles (nano γ-Fe 2 O 3 @SiO 2 @vitamin B 1 ) [47]. The methodology shows random formation of nanoparticles and does not get the specific shape and size of nanomaterials.…”
Section: Catalytic Application Of γ-Fe 2 O 3 Nanoparticlesmentioning
“…Recently, the Azizi and Heydari reported acylation of phenols and alcohols using vitamin B 1 supported on silica-encapsulated γ-Fe 2 O 3 nanoparticles (nano γ-Fe 2 O 3 @SiO 2 @vitamin B 1 ) [47]. The methodology shows random formation of nanoparticles and does not get the specific shape and size of nanomaterials.…”
Section: Catalytic Application Of γ-Fe 2 O 3 Nanoparticlesmentioning
“…The torsion degree of the pyrophosphate side chain for compound 1 is close to the degree of compound Hg(2-(α-hydroxybenzyl)thiamin)Cl 3 .H 2 O (4) in the literature, and also the host molecule of 4 is TPP, [40] whereas the torsion degree of the phosphate side chain for compounds 2 and 3 is found to be different from the ones of (TMP)(Hg 2 Br 5 )·0.5H 2 O (5) in the literature. [41] It should be noted that the sulfur atom of the thiazole ring for compound 2 has a weak interaction with O5D1 atom of the phosphate group (O5D 1 ···S1 = 3.0089 Å), which is nearly approaching to the contact distance 2.949(10) Å for Pt(thiamine)(NO 2 ) 3 (6) in the literature; [42] however, for compounds 1 and 3, the interactions are between the electropositive S1 atom and oxygen atom in the anions, and it occurred in other publication that no close contact exists between the sulfur atom of the thiazole ring and the O atom from the side chain, such as in compound 5. [41] The reason may be the effect produced by different anions or coordination anions, being affected by the electron-withdrawing of metallic atom cadmium in compound 2; the torsion angle of 2 is much larger than that of the other two compounds.…”
Section: Structure Of Compoundmentioning
confidence: 98%
“…[5][6][7][8][9][10] The decarboxylation of α-keto acids is a key intermediate process in carbohydrate metabolic reactions. In addition, α-keto acids can also participate in catalyzed condensation reaction, reduction reaction and biochemistry synthesis.…”
(3) (TPP = thiamine pyrophosphate, TMP = thiamine monophosphate) were synthesized in methanol or water systems at room temperature. They were characterized by elemental analysis, IR spectrocopy, and single X-ray
“…[9] Surface functionalization of magnetic nanoparticles (MNPs) is a well-designed way to bridge the gap between heterogeneous and homogeneous catalysis. [10][11][12] Organocatalysts contain a homogeneous part whereby starting materials are easily converted to the desired products(s), and the heterogeneous part of these advanced catalysts can be separated easily using an external magnet. [13][14][15] Thus, high conversions in reaction and easy work-up procedures allow the preparation of desired compounds in high pure isolated yields.…”
Fe3O4@vitamin B1 was designed and prepared as an inexpensive and efficient heterogeneous nanocatalyst for the synthesis of new 1,3‐thiazol derivatives. The structure of the nanomagnetic catalyst was comprehensively characterized using Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, energy‐dispersive X‐ray spectroscopy, vibrating sample magnetometry and thermogravimetric analysis. The three‐component, one‐pot condensation of arylglyoxal monohydrate, cyclic 1,3‐dicarbonyls and thioamides in water as a green solvent was applied for the preparation of 1,3‐thiazol derivatives. Simple preparation of the catalyst from commercially available materials, high catalytic activity, simple operation, short reaction times, high yields and use of green solvent are some advantages of this protocol. The superparamagnetic nanocatalyst is magnetically separable and retains its stability after recycling for at least five consecutive runs without detectable activity loss.
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