Reaction Of Alkynes Research Articles

Immobilized nickel nanoparticles on modified magnetic titanium dioxide: A proficient and eco-friendly nanocatalyst for the green A3-coupling synthesis of propargylamines

In this research, a novel and highly efficient magnetic catalyst was synthesized by surface modification of Fe3O4/TiO2 with epibromohydrine and N-(2-aminoethyl)piperazine linkers and then by immobilization of Ni nanoparticles onto the surface of magnetic titanium dioxide. The synthesized Fe3O4/TiO2-EP-NAEP/Ni nanocomposite was identified by FT-IR, PXRD, TEM, FE-SEM, ICP, EDX, TGA, and VSM techniques, and its catalytic performance was investigated in an A3 coupling reaction of amines, various aldehyde, and terminal alkynes in solvent-free conditions and propargylamine derivatives was gained with excellent yields. Also, the catalyst has high recyclability and can be reused at least six times in the synthesis of propargylamine derivatives with good yields.

Syn-Aminoauration versus Anti-Aminoauration of Alkynes in Au(I)/Au(III) Catalysis: Understanding the Origin of Selectivity.

There is no experimental evidence of whether such gold-catalyzed aminoauration reactions follow the anti- and/or syn-pathway, and hence, to understand the origin of the selectivity in Au(I)- and Au(III)-catalyzed reactions of alkynes, a thorough mechanistic study was performed using DFT methods. The NBO and ASM analyses provided significant information about the structure-stability-reactivity of the pathway-determining states (PDS). This study further reveals that the oxidation states and geometries of gold, the steric bulk, and the dihedral angles of the PDS direct the mechanistic pathways and control the turnover frequency.

Organocatalytic Atroposelective Reactions of Alkynes

AbstractThe atroposelective transformation of alkynes is an efficient protocol for the assembly of axially chiral compounds. Benefitting from the rapid development of chiral organocatalysts, the organocatalytic atroposelective reactions of alkynes have been extensively studied over the past decades. An array of chiral catalysts, including chiral Brønsted acid catalysts, secondary amine catalysts, N-heterocyclic carbene (NHC) catalysts, thiourea catalysts and N-squaramide catalysts, are employed in enantioselective reactions of different alkynes. This short review summarizes the recent advances on organocatalytic atroposelective reactions of alkynes according to the type of alkyne substrate. The reaction mechanisms, modes of enantiocontrol, product diversity and applications are highlighted.1 Introduction2 Electron-Rich Aryl Alkynes3 Electron-Deficient Aryl Alkynes4 Other Types of Alkynes5 Conclusion and Outlook

Copper (II) complex supported on magnetic nanoparticles as a novel nanocatalyst for the synthesis of imidazo[1,2-a]pyridines.

Research on the synthesis of imidazo[1,2-a]pyridines has gained great importance among synthetic chemists because there have been numerous reports of their biological and medicinal activities. In this respect, we fabricated CuCl2 immobilized on Fe3O4 nanoparticles modified with 1,10-phenanthroline-5,6-diol [Fe3O4@Diol/Phen-CuCl2] and investigated its catalytic activity for the preparation of imidazo[1,2-a]pyridine derivatives through one-pot three-component reaction of 2-aminopyridines, aldehydes and terminal alkynes under ecofriendly conditions. FT-IR spectroscopy, EDX, SEM, TEM, XRD, TGA, VSM and ICP-OES techniques employed in order to identify the structure of the as-constructed Fe3O4@Diol/Phen-CuCl2 nanocatalyst. This catalytic system has a series of advantages such as the synthesis of imidazo[1,2-a]pyridine products with high yields in suitable time, performing the reactions in an environmentally friendly solvent (PEG), easy preparation of the catalyst with a simple method, and the recyclability of the Fe3O4@Diol/Phen-CuCl2 nanocatalyst.

Perspectives on push-pull chromophores derived from click-type [2 + 2] cycloaddition-retroelectrocyclization reactions of electron-rich alkynes and electron-deficient alkenes.

Various push-pull chromophores can be synthesized in a single and atom-economical step through [2 + 2] cycloaddition-retroelectrocyclization (CA-RE) reactions involving diverse electron-rich alkynes and electron-deficient alkenes. In this review, a comprehensive investigation of the recent and noteworthy advancements in the research on push-pull chromophores prepared via the [2 + 2] CA-RE reaction is conducted. In particular, an overview of the physicochemical properties of the family of these compounds that have been investigated is provided to clarify their potential for future applications.

Mild Metal-Free 1,2-Dichlorination of Alkynes by NCS-PPh3-H2O System

AbstractFacile dichlorination of alkynes to give 1,2-dichloroalkenes is described. Previous studies for the synthesis of the 1,2-dichloroalkenes from the corresponding alkynes require stoichiometric amount of copper salt, preparation of the chlorinating reagent from hazardous compounds such as molecular chlorine, and highly acidic conditions. In this paper, only ubiquitous reagents, NCS-PPh3-H2O, are used to prepare the 1,2-dichloroalkenes from the alkynes under mild conditions. Various functional groups such as esters, ethers or carbamates were tolerated under these reaction conditions.

Synthesis and characterization of a new copper-based polyoxomolybdate and its catalytic activity for azide-alkyne cycloaddition reaction under UV light irradiation

A new organic-functionalized Cu-based Anderson-type polyoxomolybdate, namely (C7H15N4)2[Na(H2O)4]2[C6H12CuMo6N2O24]·2(H2O) (CuII-POM), was synthesized via a simple one-pot reaction and subsequently characterized using a range of analytical and spectral techniques. Structural investigation by single crystal X-ray diffraction analysis revealed that the polyanion component of the synthesized compound (i.e. [C6H12CuMo6N2O24]4−) possesses a δ-isomer Anderson-type structure, which is surrounded by four lattice water molecules and four [C7H15N4–NaH15(H2O)8]4+ cations in the crystal packing arrangement. The resulting double-sided tris-functionalized Anderson-type compound can function as highly effective heterogeneous photocatalysts for the copper(I)-catalyzed Huisgen azide-alkyne cycloaddition (Cu-AAC) reaction of terminal alkyne, benzyl halides, and sodium azide (acts as the azidonation and reducing agent) in aqueous media. Ultraviolet light irradiation enhances the catalytic activity of CuII-POM ~ 4.4 times of the “off” situation under reaction conditions of 0.00239 mmol cat., 80 °C, 8 h, 2 mL H2O, So that the isolated yields for the AAC reaction involving a variety of terminal alkynes and benzyl halides using the CuII-POM catalyst ranged between 19–97%. The current study is the first report about using an efficient and economical Cu(II)-POM/UV/NaN3 catalytic system in the Cu-AAC reaction and reveals its significant potential for applying to other Cu(I)-catalyzed reactions.

Reactions of alkynes with C-S bond formation: recent developments.

Alkynes are important in organic synthesis. This review mainly focuses on recent advances (2013-2023) on alkynes with C-S bond formation, based on more than 30 types of sulfur reagents. The reactions of alkynes with various sulfur-containing compounds including RSSR (disulfides), RSH (thiols), S8 (elemental sulphur), alkynyl thioethers, RSCN, AgSCF3, K2S, Na2S, dithiane, RSCl, NFSI, RNCS, EtOCS2K, thiocarbamate, RSONH2, thiourea, sulfoxide, RSO2N3, CS2, RSO2NH2, RSO2NHNH2, RSO2Cl, RSO2Oar, RSO2SR', DABCO·(SO2)2, Na2S2O5, K2S2O5, RSO2H, RSO2Na and related compounds are discussed. Diverse mechanisms such as radical, electrophilic/nucleophilic addition, rearrangement, C-C bond cleavage, and CuAAC are discussed. The content is organized by substrates and reactivity patterns. We hope it will help in future research in this area.

The reaction of acetylenes with aldazines in the NaOBut/DMSO system: a contribution to the pyrazole chemistry

Arylacetylenes readily react with aromatic aldazines in superbase medium NaOBut/DMSO (1 vol% EtOH) at room temperature to afford mainly 4-arylmethyl-3,5-diaryl-1H- pyrazoles in up to 47% yield along with minor amounts of 1-arylmethyl-3,5-diaryl-1H-pyrazoles and 1,2-diaryl-1,2- bis(3,5-diaryl-1H-pyrazol-1-yl)ethanes. The reaction is rationalized as proceeding via the diazaallyl anions, the adducts of acetylenic carbanions to a C=N bond, which further undergo the proton transfer processes and intramolecular cyclization to the above pyrazole derivatives.

Mechanistic study of the atomic layer deposition of cobalt: a combined mass spectrometric and computational approach.

Cobaltcarbonyl-tert-butylacetylene (CCTBA) is a conventional precursor for the selective atomic layer deposition of Co onto silicon surfaces. However, a limited understanding of the deposition mechanism of such cobalt precursors curbs rational improvements on their design for increased efficiency and tuneable selectivity. The impact of using a less reactive internal alkyne instead of a terminal alkyne was investigated using experimental and computational methods. Using electrospray-ionization mass spectrometry, the formation of CCTBA analogs and their gas phase decomposition pathways were studied. Decomposition experiments show very similar decomposition pathways between the two complexes. The internal alkyne dissociates from the Co complex at slightly lower energies than the terminal alkyne, suggesting that an internal alkynyl ligand may be more suited to low temperature ALD. In addition, transition state calculations using the nudged elastic band method confirm an increased reaction barrier between the internal alkyne and the Si-H surface bonds on Si(111). These results suggests that using a less reactive internal alkyne will result in fewer embedded carbon impurities during deposition onto Si wafers. DFT calculations using the PBE functional and periodic boundary conditions also predict increased surface binding with the metal centers of the internal alkynyl complex.

Advances in the Synthesis of Organogermaniums Based on the Addition Reactions of Alkenes and Alkynes

Advances in the Synthesis of Organogermaniums Based on the Addition Reactions of Alkenes and Alkynes

Direct trifluoromethylthiolation of terminal alkynes mediated by a hypervalent trifluoromethylthio-iodine(iii) reagent; boosting effect of fluorinated alcohol

We reported a direct simple trifluoromethylthiolation reaction of various terminal alkynes using a new hypervalent trifluoromethylthio-iodine(iii) reagent TFTI in a fluorinated alcohol, either hexafluoro-2-propanol or perfluoro-tert-butanol.

Utilizing perhalopyridine-based alkynes as suitable precursors for the synthesis of novel poly(1,2,3-triazolyl)-substituted perhalopyridines.

A novel series of poly(1,2,3-triazolyl)-substituted perhalopyridines 5a-f were successfully synthesized from the click reaction of the terminal alkynes (drived from the nucleophilic substitution reactions of PFP 1a and PCP 1b with excess amounts of propargyl alcohol) with aryl azides 4a-c under ultrasonic irradiation. Likewise, the sonication of reaction mixtures containing pyridyl cores 3, alkyl bromides 6a,b, and NaN3 under one-pot conditions afforded their respective aliphatic 1,2,3-triazoles 7a-d in yields ranging from 71% to 83%. We next developed an effective method for the regioselective preparation of 2,3,4,5-tetrachloro-6-(prop-2-yn-1-yloxy)pyridine 3c through SNAr reaction of PCP with propargyl alcohol without the utilization of any catalyst. It was then used to fabricate several ((1,2,3-triazol-4-yl)methoxy)-3,4,5,6-tetrachloropyridines 8a-c under the reaction conditions. Finally, the Pd(PPh3)4-catalyzed SMC reaction of tris-triazoles 5b,e with arylboronic acids 9a-c offered a practical method for the synthesis of biaryl-embedded poly(1,2,3-triazoles) 10a-f in good yields.

Recent advances in the applications of gem-difluoromethylene alkynes.

As a special class of alkynes, gem-difluoromethylene alkynes exhibit a variety of fascinating properties due to the presence of the gem-difluoro substitution. This substitution highlights the distinctive fluorine effects in influencing the chemoselectivity of reactions. As a result, chemical scientists have shown great interest and enthusiasm for investigating their reactions. In this review, we briefly summarize recent advances in transition metal-catalysed reactions of gem-difluoromethylene alkynes with multiple reaction pathways. Their mechanistic studies and challenges will be highlighted. The purpose of this review is to provide illustrations of elegant gem-difluoromethylene alkynes and thereby elicit further interest among synthetic chemists in developing innovative transformations of gem-difluoromethylene alkynes.

A highly sensitive and selective fluorescent biosensor for breast cancer derived exosomes using click reaction of azide-CD63 aptamer and alkyne-polymer dots.

Exosomes have gained recognition as valuable reservoirs of biomarkers, holding immense potential for early cancer detection. Consequently, there is a pressing need for the development of an economical and highly sensitive exosome detection methodology. In this work, we present a fluorescence method for breast cancer-derived exosome detection based on Cu-triggered click reaction of azide-modified CD63 aptamer and alkyne functionalized Pdots. The detection threshold for the exosomes obtained from the breast cancer serum was determined to be 6.09 × 107 particles per μL, while the measurable range spanned from 6.50 × 107 to 1.30 × 109 particles per μL. The employed methodology achieved notable success in accurately distinguishing breast cancer patients from healthy individuals through serum analysis. The application of this method showcases the significant potential for early exosome analysis in the clinical diagnosis of breast cancer patients.

Unprecedented Mo3S4 cluster-catalyzed radical C-C cross-coupling reactions of aryl alkynes and acrylates.

A new method for the generation of benzyl radicals from terminal aromatic alkynes has been developed, which allows the direct cross coupling with acrylate derivatives. Our additive-free protocol employs air-stable diamino Mo3S4 cubane-type cluster catalysts in the presence of hydrogen. A sulfur-centered cluster catalysis mechanism for benzyl radical formation is proposed based on catalytic and stoichiometric experiments. The process starts with the cluster hydrogen activation to form a bis(hydrosulfido) [Mo3(μ3-S)(μ-S)(μ-SH)2Cl3(dmen)3]+intermediate. The reaction of various aromatic terminal alkynes containing different functionalities with a series of acrylates affords the corresponding Giese-type radical addition products.

Electrochemical stereoselective synthesis of polysubstituted 1,4-dicarbonyl Z-alkenes via three-component coupling of sulfoxonium ylides and alkynes with water.

The first straightforward strategy for the synthesis of 1,4-dicarbonyl Z-alkenes has been developed via an electrochemical cross-coupling reaction of sulfoxonium ylides and alkynes with water. The metal-free protocol showed an easy-to-handle nature, good functional group tolerance, and high Z-stereoselectivity, which is rare in previous cases. The proposed reaction mechanism was convincingly established by carrying out a series of control experiments, cyclic voltammetry experiments, and density functional theory (DFT) studies.

Silanes as a versatile hydride source for Ni–H catalysis: a promising tool for π-hydro functionalization

Nickel-catalyzed hydrofunctionalization of π-substrates is a possibly effective method to synthesize several value-added molecular architectures. This review covers the NiH catalyzed hydrofunctionalization reactions of alkenes, alkynes and allenes.

Bench-stable Nickel(II)–aryl Complex-Catalyzed cyclotrimerisation of diynes and alkynes to synthesis multisubstituted benzene derivatives

Herein, we report a (PPh3)2Ni(o-tolyl)Cl complex-catalyzed cyclotrimerisation reaction of diynes and alkynes to furnish multi-substituted benzene derivatives in moderate to excellent yields. This method features an air-stable catalyst, green reaction conditions, and excellent functional group tolerance. Additionally, this approach enables gram-scale synthesis, and the target product could also be further derivatised into important isoindolinone scaffolds. These demonstrate the potential application of this methodology.

Zinc amidinate-catalysed cyclization reaction of carbodiimides and alkynes. An insight into the mechanism.

A synthesis of iminopyridines based on zinc has been developed. The commercially available ZnEt2 was employed as a precatalyst for this process. A mechanism has been proposed on the basis of Density Functional Theory (DFT) studies and stoichiometric reactions. The zinc amidinato intermediates underscore the critical role of zinc in this synthesis process.