Oxidative Cross-coupling Research Articles

Immobilization of laccase on mesoporous metal organic frameworks for efficient cross-coupling of ethyl ferulate.

Laccases act as green catalysts for oxidative cross-coupling of phenolic antioxidnt compounds, but low stability and non-recyclability limit its application. To address that, metal-organic frameworks Cu-BTC and Cr-MOF were synthesized as supports to immobilize the efficient laccase from Cerrena sp. HYB07. The Brunauer-Emmett-Teller surface area of Cu-BTC and Cr-MOF were 1213.2 and 907.1m2/g, respectively. The two carriers respectively presented pore diameters of 1.2-10nm and 1.4-12nm as octahedron, indicating nano-scale mesoporosity. These Cu-BTC and Cr-MOF carriers could adsorb laccase with enzyme loading of 1933.2 and 1564.4U/g carrier, respectively. The stability and organic solvent tolerance of Cu-BTC-laccase and Cr-MOF-laccase were both obviously improved compared to free laccase. Thermal inactivation kinetics showed that both the two immobilized laccases displayed lower thermal inactivation rate constants. Importantly, the Cu-BTC-laccase and Cr-MOF-laccase both showed much higher activity for cross-coupling of ethyl ferulate than free laccase, which had 2.5-fold higher cross-coupling efficiency than that by free laccase. The ethyl ferulate coupling product was also analyzed by mass spectroscopy and the synthesis pathway of ethyl ferulate dimer was proposed. The cross coupling of ethyl ferulate required the formation of radical intermediates of ethyl ferulate generated by laccase mediated oxidation. This work paved the way for MOFs immobilized laccase for cross coupling of antioxidant phenols.

Revisiting the early days of conjugated polyyne synthesis. Syntheses and structures of Bis(triethylsilyl) Polyynediyl Adducts Et3Si(C[tbnd]C)nSiEt3 previously regarded as Unisolable (n = 6, 8, 12)

An overview of bis(trialkylsilyl) polyynediyl adducts R3Si(CC)nSiR3 with n ≥ 5 is followed by syntheses of TESCxTES where x = 8, 12, 16, and 24 (TES = SiEt3; x = 2n). In a seminal 1972 study, the last three were presented as too unstable to isolate and thus only characterized by UV-visible spectroscopy. Although not a rational route, TESC24TES is consistently obtained from the reaction of trans-(C6F5)(p-tol3P)2Pt(CC)5SiEt3 and crude HC8TES under Hay oxidative cross coupling conditions. The latter contains some HC8H and TESC8TES. Hay oxidative homocouplings of HC4TES and crude HC8TES afford TESC8TES (83%) and TESC16TES (5%). A Cadiot-Chodkiewicz reaction of BrC4Br and HC4TES (2 equiv) yields TESC12TES (11%). All of these compounds are crystalline, and the crystal structures of TESC8TES and TESC16TES are determined. The 13C{1H} NMR and UV-visible properties are also compared.

On the Existence and Relevance of Copper(III) Fluorides in Oxidative Trifluoromethylation

AbstractNumerous reports invoke CuIII–F intermediates engaging in oxidative cross-couplings mediated by low/mid-valent copper and formal sources of ‘F+’ oxidants. These elusive and typically instable CuIII fluorides have been rarely characterized or spectroscopically identified, making their existence and participation within catalytic cycles somehow questionable. We have authenticated a stable organocopper(III) fluoride that undergoes Csp–CF3 bond formation upon addition of silyl-capped alkynes following a 2 e– CuIII/CuI redox shuttle. This finding strongly supports the intermediacy of CuIII fluorides in C–C coupling. We review herein the state of the art about well-defined CuIII fluorides enabling cross-coupling reactions.1 Introduction2 Brief History of Coupling-Competent CuIII Fluorides3 Design of an Isolable – yet Reactive – Organocopper(III) Fluoride4 Alkyne Trifluoromethylation: Scope and Mechanism5 Extension to Aryl–CF3 and C–Heteroatom Couplings6 Summary and Outlook

Cobalt/Salicylaldehyde-Enabled C-H Alkoxylation of Benzamides with Secondary Alcohols under Solvothermal Conditions.

C-O bond formation via C-H alkoxylation remains a challenge, especially coupling with a secondary alcohol, due to its low activity and sterically encumbered property. Here, we report a general and effective cobalt-catalyzed oxidative cross-coupling of benzamides with secondary alcohols via C-H alkoxylation reaction under solvothermal conditions, enabled by a salicylaldehyde/cobalt complex. The protocol features easy operation without additives, broad substrate scope, and excellent functional tolerance. The applicability is proven by the gram-scale synthesis and modification of natural products.

Rhodium(III)-Catalyzed Oxidative Cross-Coupling of N-Pyrimidylindoles with Cyclic β-Keto Esters for Accessing All-Carbon Quaternary Centers.

Rh(III)-catalyzed direct oxidative C-H/C-H cross-coupling between N-pyrimidylindoles and β-ketoesters is presented. Easily available β-ketoesters are used as an alkylating agent for the facile construction of all-carbon quaternary centers under mild conditions. The ester group in the product can undergo decarboxylation or decarboxylative amination.

Para-selective nitrobenzene amination lead by C(sp2)-H/N-H oxidative cross-coupling through aminyl radical

Arylamines, serving as crucial building blocks in natural products and finding applications in multifunctional materials, are synthesized on a large scale via an electrophilic nitration/reduction sequence. However, the current methods for aromatic C–H amination have not yet attained the same level of versatility as electrophilic nitration. Here we show an extensively investigated transition metal-free and regioselective strategy for the amination of nitrobenzenes, enabling the synthesis of 4-nitro-N-arylamines through C(sp2)-H/N-H cross-coupling between electron-deficient nitroarenes and amines. Mechanistic studies have elucidated that the crucial aspects of these reactions encompass the generation of nitrogen radicals and recombination of nitrobenzene complex radicals. The C(sp2)-N bond formation is demonstrated to be highly effective for primary and secondary arylamines as well as aliphatic amines under mild conditions, exhibiting exceptional tolerance towards diverse functional groups in both nitroarenes and amines (>100 examples with yields up to 96%). Notably, this C(sp2)-H/N-H cross-coupling exhibits exclusive para-selectivity.

Electrochemical Oxidative Cross-Coupling Reactions of Ketene Dithioacetals and Dichalcogenides to Construct C−Se/C−S Bonds

A green protocol for construction of C−Se bonds from ketene dithioacetals and diselenides through direct electrochemical oxidative cross-coupling has been developed. This reaction was carried out in an undivided cell system with NaBF4 as the electrolyte and CH3CN as the solvent through galvanostatic electrolysis. A series of substituted ketene dithioacetals and diselenides were tolerant and the desired tetrasubstituted alkenyl selenides were obtained in moderate to excellent yields. In addition, construction of C−S bond from ketene dithioacetals and disulfides through electrochemical method in the presence of KI was also successfully realized. It exhibited high efficiency and broad functional group tolerance.

Stereoselective amino acid synthesis by photobiocatalytic oxidative coupling.

Photobiocatalysis-where light is used to expand the reactivity of an enzyme-has recently emerged as a powerful strategy to develop chemistries that are new to nature. These systems have shown potential in asymmetric radical reactions that have long eluded small-molecule catalysts1. So far, unnatural photobiocatalytic reactions are limited to overall reductive and redox-neutral processes2-9. Here we report photobiocatalytic asymmetric sp3-sp3 oxidative cross-coupling between organoboron reagents and amino acids. This reaction requires the cooperative use of engineered pyridoxal biocatalysts, photoredox catalysts and an oxidizing agent. We repurpose a family of pyridoxal-5'-phosphate-dependent enzymes, threonine aldolases10-12, for the α-C-H functionalization of glycine and α-branched amino acid substrates by a radical mechanism, giving rise to a range of α-tri- and tetrasubstituted non-canonical amino acids 13-15 possessing up to two contiguous stereocentres. Directed evolution of pyridoxal radical enzymes allowed primary and secondary radical precursors, including benzyl, allyl and alkylboron reagents, to be coupled in an enantio- and diastereocontrolled fashion. Cooperative photoredox-pyridoxal biocatalysis provides a platform for sp3-sp3 oxidative coupling16, permitting the stereoselective, intermolecular free-radical transformations that are unknown to chemistry or biology.

Redox Relay-Induced C-S Radical Cross-Coupling Strategy: Application in Nontraditional Site-Selective Thiocyanation of Quinoxalinones.

Oxidative cross-coupling is a powerful strategy to form C-heteroatom bonds. However, oxidative cross-coupling for constructing C-S bond is still a challenge due to sulfur overoxidation and poisoning transition-metal catalysts. Now, electrochemical redox relay using sulfur radicals formed in situ from inorganic sulfur source offers a solution to this problem. Herein, electrochemical redox relay-induced C-S radical cross-coupling of quinoxalinones and ammonium thiocyanate with bromine anion as mediator is presented. The electrochemical redox relay comprised initially the formation of sulfur radical via indirect electrochemical oxidation, simultaneous electrochemical reduction of the imine bond, electro-oxidation-triggered radical coupling involving dearomatization-rearomatization, and the reformation of the imine bond through anodic oxidation. Applying this strategy, various quinoxalinones bearing multifarious electron-deficient/-rich substituents at different positions were well compatible with moderate to excellent yields and good steric hindrance compatibility under constant current conditions in an undivided cell without transition-metal catalysts and additional redox reagents. Synthetic applications of this methodology were demonstrated through gram-scale preparation and follow-up transformation. Notably, such a unique strategy may offer new opportunities for the development of new quinoxalinone-core leads.

Electrochemically Enable N-Sulfenylation/Phosphinylation of Sulfoximines via Oxidative Dehydrocoupling Reaction.

An electrochemical oxidative cross-coupling strategy for the synthesis of N-sulfenylsulfoximines from sulfoximines and thiols was accomplished, giving diverse N-sulfenylsulfoximines in moderate to good yields. Moreover, this strategy can be extended to construct the N-P bond of N-phosphinylated sulfoximines. With electrons as reagents, the oxidative dehydrogenation cross-coupling reaction proceeds smoothly in the absence of traditional redox reagents.

Electrochemical Synthesis of Selenosulfonates from Diselenides and Sulfonyl Hydrazides.

The electrochemical oxidative radical-radical cross-coupling of sulfonyl hydrazides with diselenides for the synthesis of selenosulfonates was successfully accomplished. The method is applicable to a wide range of aromatic/aliphatic sulfonyl hydrazides and diselenides, providing products in good to excellent yields. Notably, this protocol stands out for its green and sustainable nature, as it does not rely on transition metals and oxidizing agents, and the starting materials are cost-effective and readily available.

CuI-Catalyzed Radical Reaction of Benzimidates to Form Valuable 4,5-Dihydrooxazoles through Regioselective Aerobic Oxidative Cross-Coupling.

A straightforward Cu(I)-catalyzed oxidative cross-coupled organic transformation has been developed under mild conditions for the construction of functionalized 4,5-dihydrooxazoles through a four-bond-forming regiocontrolled C-C/C-N/C-O coupling strategy emerging benzimidates, paraformaldehyde, and 1,3-diketo analogues using eco-friendly O2 as the sole oxidant. The fundamental features of these designed approaches involve operational simplicity, selectivity, generality, and a broad substrate scope with high yields under the same reaction conditions.

Visible Light-Promoted Oxidative Cross-Coupling of Alcohols to Esters

Ester is one of the most significant functional groups in organic chemistry and is enclosed in several valued molecules. Usually, esters are prepared through the acid-catalyzed esterification reaction of carboxylic acids with alcohols, transesterification of esters with alcohols, or via activation of carboxylic acids followed by the addition of alcohols. However, these procedures typically imply the excess use of reactants and harsh reaction conditions. Visible light-mediated photoreactions have been disclosed to display a safe, sustainable, and accessible alternative to traditional methods, and to lead new reactivity modes in organic procedures. In this context, we propose a transition metal-based and organic-based photocatalyst-free synthesis of esters from alcohols induced by visible light. The methodology can be carried out using sunlight or artificial visible light as a solar simulator or a blue LED source.

Visible-Light-Promoted Metal- and Photocatalyst-Free Reactions between Arylglyoxylic Acids and Tetraalkylthiuram Disulfides: Synthesis of α-Ketoamides.

A convenient and new synthetic approach has been developed for the oxidative cross-coupling of the C-N bond through the reaction between arylglyoxylic acids and tetraalkylthiuram disulfides. The reaction proceeds under ambient air at room temperature in the presence of visible light. This reaction offers a metal-, base-, photocatalyst-, and solvent-free synthesis of various α-ketoamides with moderate to excellent yields via the radical pathway. In addition, this protocol demonstrates the potential application of a gram-scale synthesis.

Electrochemical oxidative cross coupling of NH-sulfoximines with disulfides

An electrochemical method for thioetherification of NH-sulfoximines with disulfides is reported. The utilization of electrochemistry for facilitating these reactions eliminates the necessity for external oxidants, bases, and metal catalysts.

Electrochemical oxidative cross-coupling of tetrahydroquinolines and azoles

An electrochemical method is described for the direct oxidative C–N coupling of tetrahydroquinolines and azoles, enabling the synthesis of dihydroquinoline-azole and quinoline-azole derivatives under mild reaction conditions.

Polyoxometalate-supported transition metal complexes for the oxidative cross-coupling of amines and alcohols.

Three new hybrid polyoxometalates (POMs) based on transition metals, namely, copper metal with γ-[Mo8O26]4- polyoxometalates [Cu(DMF)4(Mo8O26)·2C3H8NO]·1.8 DMF (1), cobalt metal with hexamolybdate [Co(DMSO)6][Mo6O19] (2), and nickel metal with hexamolybdate [Ni(DMSO)6][Mo6O19] (3), were developed. These materials were characterised by applying both analytical and spectroscopic techniques (IR, TGA, and CHNO elemental analysis), and structural elucidation was performed using single-crystal X-ray diffraction studies. Among these hybrid POMs, octamolybdate with copper was used for the catalytic production of benzimidazoles. The incorporation of [Cu(DMF)4] between two octamolybdates results in the transformation of POMs into a useful catalyst, which effectively catalyses the oxidative cross-coupling of anilines, benzyl alcohol, and sodium azide to produce benzimidazole. This catalytic reaction occurs in the presence of tert-butyl hydroperoxide (TBHP) at a moderate temperature. Benzimidazole and its derivatives are highly preferred owing to their wide-ranging biological activities and clinical applications. These compounds are exceptionally effective in terms of their selectivity ratio and inhibitory activity. The catalytic reaction presented herein is a one-pot procedure that includes a series of reactions, such as C-H functionalization, condensation, ortho selective amination, and cyclization.

Metal–organic framework-catalyzed selective oxidation of alcohols and oxidative cross-coupling for C–C and C–N bond-forming reactions

A novel porous metal–organic framework Co(btc)(bpy) (Co-MOF-3a) was synthesized by employing a bipyridyl ligand, benzene tricarboxylic acid, and Co(NO3)2·6H2O and was completely characterized.

Straightforward α-allylation of carbonyl compounds with alkenes via α-carbonyl radical intermediates

We report that the direct oxidative cross-coupling of carbonyl compounds with simple alkenes is realized to synthesize α-allylated carbonyl compounds by identifying the bisphosphine ligand BINAP that enables the copper catalyst to integrate two different catalytic cycles in a one-pot system.

One-pot thermo-induced radical-radical oxidative cross-coupling for symmetrical dimeric thiadiazole monosulfide formation

The production of heterocyclic sulfide is the key building block in various applications, especially in the field of medicinal chemistry. Currently, heterocyclic sulfide was synthesized via deoxygenation of sulfoxide or cross coupling between sulfur sources and halogen compounds. However, these conventional methods suffer from drawbacks such as the use of toxic solvents, harsh reaction conditions, the requirement for transition metal catalysts, inert conditions, and the generation of toxic and corrosive halide-containing waste. In this study, a milder approach using hydrogen peroxide-mediated oxidative cross-coupling of 5-alkylsulfanyl-[1,3,4]thiadiazole-2-thiol successfully produces symmetrical dimeric thiadiazole monosulfide with an isolated yield of 73‒87 %. The molecular structure of bis(2-octylsulfanyl-[1,3,4]thiadiazolyl)-5,5′-sulfide was confirmed by X-ray crystal structure analysis. Interestingly, the formation of dimeric thiadiazole monosulfide undergoes a one-pot thermo-induced pathway. Density functional theory (DFT) indicates the formation of thiadiazole monosulfide is thermodynamically favorable through the cross-coupling reaction between thiadiazole thiyl radical and thiadiazole carbon-centered radical.