Amines are important and valuable compounds widely used in the chemical industry to produce various products such as dyes, detergents, solvents, additives, pharmaceutical products, and anti-foam agents. A property that distinguishes primary amines from other compounds is their straightforward functionalization. Therefore, the synthesis of different amine compounds has been considered by many researchers in recent years. Usually, primary amines are produced via amination of alcohols, reductive amination, and reduction of nitro and amide compounds. Furthermore, a useful and atom-economical method for producing primary amines is reducing nitrile compounds using catalytic systems. Traditionally, nitriles are reduced using metal hydrides such as LiAlH4 or NaBH4. These methods have important restrictions in terms of selectivity and waste generation. Hence, the heterogeneous and homogeneous catalysts were investigated for the hydrogenation of nitriles to diverse amines. This review describes the performance of different catalytic systems for reducing nitrile compounds to their corresponding amines.
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http://dx.doi.org/10.2174/0113862073284975240324091848 | DOI Listing |
J Hazard Mater
January 2025
College of Polymer Science & Engineering, Sichuan University, Chengdu 610065, China. Electronic address:
While single-atom catalysts (SACs) have been extensively investigated as a high-atom-efficiency heterogeneous catalyst for peroxymonosulfate (PMS) oxidation reaction, the stable constructing and activation efficacy of the reaction sites remains less clarified. Herein, we employed gelatin as a N,O-bidentate ligand for Co (II) to form for a N-doped carbon precursor, while introducing NaCl as a template agent to induce the adoption of a Co-N conformation and disorganize the Co-O moiety. This approach facilitates uniform spatial isolation and atomic-level dispersion of Co atoms within the aerogel, effectively inhibiting the aggregation of Co during synthesis and enabling precise and controllable preparation of Co single-atom catalysts (SACs).
View Article and Find Full Text PDFTyrosine phosphorylation is an important post-translational modification that regulates many biochemical signaling networks in multicellular organisms. To date, 46,000 tyrosines have been observed in human proteins, but relatively little is known about the function and regulation of most of these sites. A major challenge has been producing recombinant phospho-proteins in order to test the effects of phosphorylation.
View Article and Find Full Text PDFFungal highly reducing polyketide synthases (hrPKSs) are remarkable multidomain enzymes that catalyse the biosynthesis of a diverse range of structurally complex compounds. During biosynthesis, the ketosynthase (KS) and acyltransferase (AT) domains of the condensing region are visited by the acyl carrier protein (ACP) domain during every cycle, catalysing chain priming and elongation reactions. Despite their significance, our comprehension of how these steps contribute to biosynthetic fidelity remains poorly understood.
View Article and Find Full Text PDFJ Org Chem
January 2025
Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati, Assam 781039, India.
The photoacid-catalyzed synthesis of 2-deoxy glycosides is presented using stable glycosyl -[1-(-MeO-Phenyl)vinyl]benzoate (PMPVB) donors and employing the eosin Y and diphenyl disulfide (PhSSPh) catalytic system in the presence of blue LED lights. The remote activation of the alkene functionality under the photoacid catalysis followed by a 5-- cyclization led to the generation of oxocarbenium ions that were trapped to provide the glycosylated products in excellent yields and decent selectivities under mild conditions. This method is also useful for the photoacid-catalyzed synthesis of -methoxybenzyl-alkyl ethers.
View Article and Find Full Text PDFACS Nano
January 2025
Department of Physics, Chalmers University of Technology, SE-412 96 Gothenburg, Sweden.
UV-vis spectroscopy is a workhorse in analytical chemistry that finds application in life science, organic synthesis, and energy technologies like photocatalysis. In its traditional implementation with cuvettes, it requires sample volumes in the milliliter range. Here, we show how nanofluidic scattering spectroscopy (NSS), which measures visible light scattered from a single nanochannel in a spectrally resolved way, can reduce this sample volume to the attoliter range for solute concentrations in the mM regime, which corresponds to as few as 10 probed molecules.
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