Arylation Reactions Research Articles

Arylthianthrenium Salts for Triplet Energy Transfer Catalysis.

Sigma bond cleavage through electronically excited states allows synthetically useful transformations with two radical species. Direct excitation of simple aryl halides to form both aryl and halogen radicals necessitates UV-C light, so undesired side reactions are often observed and specific equipment is required. Moreover, only aryl halides with extended π systems and comparatively low triplet energy are applicable to synthetically useful energy transfer catalysis. Here we show the conceptual advantages of arylthianthrenium salts (ArTTs) for energy transfer catalysis with high energy efficiency compared to conventional aryl (pseudo)halides and their utility in arylation reactions of ethylene. The fundamental advance is enabled by the low triplet energy of ArTTs that may originate in large part from the electronic interplay between the distinct sulfur atoms in the tricyclic thianthrene scaffold, which is not accessible in either simple (pseudo)halides or other conventional sulfonium salts.

Remote Selective Cross‐Dehydrogenative Coupling Reactions of Aryl C−H Bonds with Carboxylic Acids at Room Temperature

AbstractAn efficient Pd(II)‐catalyzed remote selective cross‐dehydrogenative coupling of broadly useful synthetic building blocks biphenyl Weinreb amides with carboxylic acids is developed. This acetoxylation protocol is performed under room temperature using N‐fluorobenzene‐sulfonimide (NFSI) as the oxidant, exhibiting a wide range of functional group tolerance and affording δ‐position‐ selective products up to 85 % yield. Notably, a diverse set of carboxylic acid‐containing drugs is also found to be compatible under the current reaction conditions. Preliminary mechanistic studies indicate that this reaction presumably proceeds through a seven‐membered palladacycle intermediate.

O-p-Methoxyphenyl α-Hydroxycarboxylic Acids as Versatile Hydroxyalkylation Agents for Photocatalysis.

Reliable radical precursors are crucial for photocatalytic processes. In particular, heteroatom-stabilized radicals have attracted considerable research interest in photocatalysis. Among them, α-amino radicals have received the most attention, while the research on α-hydroxy radicals is much less developed. Herein, we present O-PMP α-hydroxycarboxylic acids as novel precursors for the formation of oxygen-stabilized radicals. These radicals have been successfully used as building blocks in Pd-catalyzed allylation reactions, Ni-catalyzed arylation and alkenylation reactions, and Giese reactions. A subsequent deprotection step liberates the corresponding hydroxyalkylation products.

Comprehensive Review on the Synthesis of [1,2,3]Triazolo[1,5-a]Quinolines.

This report outlines the evolution and recent progress about the different protocols to synthesize the N-heterocycles fused hybrids, specifically [1,2,3]triazolo[1,5-a]quinoline. This review encompasses a broad range of approaches, describing several reactions for obtaining this since, such as dehydrogenative cyclization, oxidative N-N coupling, Dieckmann condensation, intramolecular Heck, (3+2)-cycloaddition, Ullman-type coupling and direct intramolecular arylation reactions. We divided this review in three section based in the starting materials to synthesize the target [1,2,3]triazolo[1,5-a]quinolines. Starting materials containing quinoline or triazole units previously formed, as well as starting materials which both quinoline and triazole units are formed in situ. Different methods of obtaining are described, such as metal-free or catalyzed conditions, azide-free, using conventional heating or alternative energy sources, such as electrochemical and photochemical methods. Mechanistic insights underlying the reported reactions were also described in this comprehensive review.

Gold‐catalyzed Annulation between 1‐[2‐(Dimethoxymethyl)phenyl]prop‐2‐yn‐1‐yl Acetates and α‐Diazoesters or Anilines to Form Substituted Naphthoates and Indeno[1,2‐b]quinoline, Respectively.

This work describes gold‐catalyzed annulations of 1‐(2‐(dimethoxymethyl)phenyl)‐1‐prop‐2‐yn‐1‐yl acetate substrates with α‐diazo esters and anilines, respectively yielding substituted naphthoates and indeno[1,2‐b]quinoline derivatives. Our mechanistic analysis indicates 1‐methoxy‐2‐carbonyl‐1H‐indenes as their common intermediates. In the formation of naphthoates, α‐diazo ester attacks at gold‐bound intermediate via a SN2 pathway to enable a allylic methoxy substitution. For indeno[1,2‐b]quinoline derivatives, there are two main reactions, including (i) a reversible formation between intermediate and a double amine addition product and (ii) an arylation reaction of intermediate. Species N‐(phenyl((2E)‐1‐(phenylimino)‐1,3‐dihydro‐2H‐inden‐2‐ylidene)methyl)aniline was converted to indeno[1,2‐b]quinoline in the presence of gold catalyst.

1,5-Diaza-3,7-diphosphacyclooctanes (P2N2): An Underappreciated Ligand Class for Nickel- and Palladium-Catalyzed Heck-Type Cross-Couplings

Abstract1,5-Diaza-3,7-diphosphacyclooctane (P2N2) scaffolds represent a readily accessible, tunable ligand class for transition metals. However, despite their prevalence in areas such as electrocatalysis and coordination chemistry, P2N2 ligands have been rarely used to make catalysts for organic synthesis. Research into Mizoroki–Heck-type aldehyde, alcohol, and alkene arylation reactions has revealed that the P2N2 family outperforms many commonly used phosphines. This Synpacts article summarizes our work and provides a broad overview on the preparation and application of P2N2 ligands in organic synthesis. It also serves to highlight how a simple, modular class of ligands can solve contemporary challenges with transition-metal catalysis, including novel reactivity and exceptional regioselectivity.

Asymmetric Synthesis of Axially Chiral N, N‐1,2‐Pentatomic Heterobiaryl Diamines by an Organocatalytic Arylation Reaction

The utilization of axially chiral biaryl diamines has been widely acknowledged as highly advantageous structures for the advancement of chiral catalysts and ligands. This highlights their extensive range of applications in asymmetric catalysis and synthesis. Herein, we devised a direct arylation reactions of 5‐aminopyrazoles with azonaphthalenes, utilizing chiral phosphoric acid as the catalyst. This method delivers structurally novel atroposelective N, N‐1,2‐azole heteroaryl diamines with high yields (up to >98%) and good to excellent enantiomeric ratios while exhibiting a wide range of substrate compatibility.

One-pot Three-component Synthesis of Fully and Diversely Functionalized Pyrans and Spiropyrans Using Sodium Formate as Catalyst in Aqueous Ethanol at Room Temperature

Abstract: A convenient and general method has been developed for the synthesis of fully and diversely functionalized pyrans via one-pot three-component reactions of various aryl or heteroaryl aldehydes, malononitrile, and 1,3-dimethyl/1,3-diethyl-acetonedicarboxylates in the presence of a catalytic amount of sodium formate as an efficient organocatalyst in aqueous ethanol at room temperature. All the scaffolds were synthesized in excellent yields within 2.5 hours. Under the same reaction conditions, fully and diversely functionalized spiro-pyrans were also synthesized in excellent yields from the reaction of isatin, malononitrile, and 1,3-dimethyl/1,3-diethylacetonedicarboxylates. All the products were isolated pure just by simple filtration. Synthesis of fully and diversely functionalized biologically promising pyrans, excellent yields, use of organocatalyst, less toxic solvent, no column chromatographic purification, and energy efficiency are some of the major advantages of this newly developed protocol. method: In a clean test tube a magnetic stir bar, 0.5 mmol of aldehydes (1a-1i), 0.5 mmol of malononitrile (2; 0.033 g) and 0.5 mmol of 1,3-dimethylacetonedicarboxylate (3a; 0.087 g) or 1,3-diethylacetonedicarboxylate (3b; 0.101 g), 4 ml aqueous ethanol (1:1 v/v) and 20 mol% sodium formate were taken sequentially. The whole reaction mixture was stirred at room temperature for the time mentioned in Table 2. The progress of reaction was monitored by TLC. By using the same amount of catalyst and solvent the synthesis of methyl/ethyl-2'-amino-3'-cyano-6'-(2-meth/ethoxy-2-oxoethyl)-2-oxospiro[indoline-3,4'-pyran]-5'-carboxylate (6a/6b) was achieved from the reactions of 0.5 mmol of isatin (5; 0.0735 g), 0.5 mmol of malononitrile (2; 0.033 g) and 0.5 mmol of 1,3-dimethylacetonedicarboxylate (3a; 0.0871 g) or 1,3-diethylacetonedicarboxylate (3b; 0.1011 g). After the completion of each reaction, the desired products were isolated simply by filtration and subsiquent washing with aqueous ethanol (EtOH:H2O = 1:1).

A General Copper-Box System for the Asymmetric Arylative Functionalization of Benzylic, Propargylic or Allenylic Radicals.

Radical-involved arylative cross-coupling reactions have recently emerged as an attractive strategy to access valuable aryl-substituted motifs. However, there still exist several challenges such as limited scope of radical precursors/acceptors, and lack of general asymmetric catalytic systems, especially regarding the multicomponent variants. Herein, we reported a general copper-Box system for asymmetric three-component arylative radical cross-coupling of vinylarenes and 1,3-enynes, with oxime carbonates and aryl boronic acids. The reactions proceed under practical conditions in the absence or presence of visible-light irradiation, affording chiral 1,1-diarylalkanes, benzylic alkynes and allenes with good enantioselectivities. Mechanistic studies imply that the copper/Box complexes play a dual role in both radical generation and ensuing asymmetric cross-coupling. In the cases of 1,3-enynes, visible-light irradiation could improve the activity of copper/Box complex toward the initial radical generation, enabling better efficiency match between radical formation and cross-coupling.

The N,N,N′,N′-tetraphenylbenzidine-based conjugated hypercrosslinked polymers for adsorping iodine and fluorescence sensing 2,4-dinitrophenol, iodine

Although progress has been made in the development of hypercrosslinked polymers (HCPs) for iodine uptake, their fluorescence performance and fluorescence sensing performance are rare due to the lack of conjugated behavior in common HCPs. Herein, the N,N,N′,N′-tetraphenylbenzidine-based conjugated hyper-crosslinked polymers (conjugated TPB-based HCPs) were efficiently fabricated via a one-step Friedel-Crafts arylation reaction by selecting N,N,N′,N′-tetraphenylbenzidine (TPB) and N,N′-diphenyl-N,N′-di(m-tolyl)benzidine (DPDB) as the basic building blocks and p-dimethoxybenzene (DMB) as an external crosslinker which will lead to the formation of the conjugated structures. The derived TPB-based HCPs (denoted as, TPB-DMB and DPDB-DMB) possessed excellent stability and high surface areas, Their iodine adsorption capacities are up to 4.25 and 3.56 g·g−1. The high iodine adsorption is caused by chemical adsorption. The fully conjugated structure and the 3D aryl network give the conjugated TPB-based HCPs excellent luminescence properties and fluorescence sensing properties for 2,4-dinitrophenol and iodine. The fluorescence sensing mechanisms of the conjugated TPB-based HCPs for DNP and I2 includes photo-induced electron process and the resonance energy transfer process. This study provides a viable approach for the development of highly efficient iodine sorbents and fluorescence sensors of DNP and iodine for addressing environmental issues.

Room Temperature Ni‐Catalyzed Ullmann Reaction of (Hetero)aryl/Vinyl Chlorides Enabled by Silylchloride‐Activated Mn Powders

AbstractA room temperature Ni‐catalyzed Mn‐mediated homocoupling of (hetero)aryl and vinyl chlorides using Mn powders pre‐activated by trimethylsilylchloride (TMSCl) in DMA is reported. Large steric effects were observed while electronic influences from aryl chlorides proved to be rather small. High regioselectivity could be achieved between ortho‐Cl and para‐Cl/Br of aryl halides benefiting from the large steric effects. A double‐face role of TMSCl, i. e. activation of Mn powders but deactivation of nickel catalyst, was observed although TMSCl‐activated Mn powders appeared to be the privileged metallic reductant. Applications of the protocol have been demonstrated in a multigram synthesis of Daclatasvir.

Revealing the Hidden Complexity and Reactivity of Palladacyclic Precatalysts: The P(o-tolyl)3 Ligand Enables a Cocktail of Active Species Utilizing the Pd(II)/Pd(IV) and Pd(0)/Pd(II) Pathways for Efficient Catalysis.

The ligand, P(o-tolyl)3, is ubiquitous in applied synthetic chemistry and catalysis, particularly in Pd-catalyzed processes, which typically include Pd(OAc)2 (most commonly used as Pd3(OAc)6) as a precatalyst. The Herrmann-Beller palladacycle [Pd(C^P)(μ2-OAc)]2 (where C^P = monocyclopalladated P(o-tolyl)3) is easily formed from reaction of Pd(OAc)2 with P(o-tolyl)3. The mechanisms by which this precatalyst system operates are inherently complex, with studies previously implicating Pd nanoparticles (PdNPs) as reservoirs for active Pd(0) species in arylative cross-coupling reactions. In this study, we reveal the fascinating, complex, and nontrivial behavior of the palladacyclic group. First, in the presence of hydroxide base, [Pd(C^P)(μ2-OAc)]2 is readily converted into an activated form, [Pd(C^P)(μ2-OH)]2, which serves as a conduit for activation to catalytically relevant species. Second, palladacyclization imparts unique stability for catalytic species under reaction conditions, bringing into play a Pd(II)/Pd(IV) cross-coupling mechanism. For a benchmark Suzuki-Miyaura cross-coupling (SMCC) reaction, there is a shift from a mononuclear Pd catalytic pathway to a PdNP-controlled catalytic pathway during the reaction. The activation pathway of [Pd(C^P)(μ2-OH)]2 has been studied using an arylphosphine-stabilized boronic acid and low-temperature NMR spectroscopic analysis, which sheds light on the preactivation step, with water and/or acid being critical for the formation of active Pd(0) and Pd(II) species. In situ reaction monitoring has demonstrated that there is a sensitivity to the structure of the arylboron species in the presence of pinacol. This work, taken together, highlights the mechanistic complexity accompanying the use of palladacyclic precatalyst systems. It builds on recent findings involving related Pd(OAc)2/PPh3 precatalyst systems which readily form higher order Pdn clusters and PdNPs under cross-coupling reaction conditions. Thus, generally, one needs to be cautious with the assumption that Pd(OAc)2/tertiary phosphine mixtures cleanly deliver mononuclear "Pd(0)Ln" species and that any assessment of individual phosphine ligands may need to be taken on a case-by-case basis.

Double Direct C-H Bond Arylation of Thiophenes with Aryl Chlorides Catalyzed by the N-Heterocyclic Carbene-PdCl2-1-methylimidazole Complex.

With the combination of the N-heterocyclic carbene-PdCl2-1-methylimidazole complex and Cu2O, we succeeded in the first example of double direct C-H bond arylation reactions between thiophenes and aryl chlorides, giving the desired 2,5-diarylated thiophenes in moderate to high yields under suitable conditions, consistent with the density functional theory calculations.

Synthesis of Accessible Triphenylamine End‐Capped Oligothiophene Emitters for Solution Processed and Printed OLEDs

AbstractDisplays have become ubiquitous in our modern and highly interconnected lives. Complex vacuum processed multi‐stacks are widely integrated into high tech, high value products such as smart phones, while solution processed large area single‐layer OLEDs appear more adequate for basic applications focusing on recyclability such as packaging, road signage, advertising, and single‐use health care products. In this context, we report herein the design, synthesis, and characterization of an accessible series of oligothiophenes end‐capped triphenylamines that were preprepared by atom‐economical direct (hetero)arylation reactions and successfully used as emitter in solution processed devices, from lab scale to large area printed and flexible demonstrator.

One‐Step Synthesis of Chiral 9,10‐Dihydrophenanthrenes via Ligand‐Enabled Enantioselective Cascade β,γ‐Diarylation of Acids

AbstractPd(II)‐catalyzed enantioselective C−H activation has emerged as a versatile platform for constructing point, axial, and planar chirality. Herein, we present an unexpected discovery of a Pd‐catalyzed enantioselective cascade β,γ‐methylene C(sp3)−H diarylation of free carboxylic acids using bidentate chiral mono‐protected amino thioether ligands (MPAThio), enabling one‐step synthesis of a complex chiral 9,10‐dihydrophenanthrene scaffolds with high enantioselectivity. In this process, two methylene C(sp3)−H bonds and three C(sp2)−H bonds were activated, leading to the formation of four C−C bonds and three chiral centers in one pot. A plausible catalytic pathway starts with enantioselective β,γ‐dehydrogenation to form chiral β,γ‐cyclohexene. Intriguingly, this olefin serves as a norbornene‐type reagent (presumably assisted by the carboxyl directing effect), relaying two successive Catellani arylation reactions and a C−H arylation reaction to furnish chiral 9,10‐dihydrophenanthrenes along with meta‐selective homocoupling products of iodoarene.

One-Step Synthesis of Chiral 9,10-Dihydrophenanthrenes via Ligand-Enabled Enantioselective Cascade β,γ-Diarylation of Acids.

Pd(II)-catalyzed enantioselective C-H activation has emerged as a versatile platform for constructing point, axial, and planar chirality. Herein, we present an unexpected discovery of a Pd-catalyzed enantioselective cascade β,γ-methylene C(sp3)-H diarylation of free carboxylic acids using bidentate chiral mono-protected amino thioether ligands (MPAThio), enabling one-step synthesis of a complex chiral 9,10-dihydrophenanthrene scaffolds with high enantioselectivity. In this process, two methylene C(sp3)-H bonds and three C(sp2)-H bonds were activated, leading to the formation of four C-C bonds and three chiral centers in one pot. A plausible catalytic pathway starts with enantioselective β,γ-dehydrogenation to form chiral β,γ-cyclohexene. Intriguingly, this olefin serves as a norbornene-type reagent (presumably assisted by the carboxyl directing effect), relaying two successive Catellani arylation reactions and a C-H arylation reaction to furnish chiral 9,10-dihydrophenanthrenes along with meta-selective homocoupling products of iodoarene.

Synthesis of α-hydroxyketones via palladium-catalyzed arylation of arylglyoxals

A palladium-catalyzed arylation reaction of arylglyoxals with arylboronic acids has been achieved. The reaction produces various acyclic α-hydroxyketones in high yields under mild conditions. Of merits mention, the rigorous exclusion of air and moisture is not required in these transformations, offering a straightforward and practical approach for the synthesis of α-hydroxyketones.

Functionalized Phosphorus‐Doped Porous Organic Polymers (FPPOPs)‐Promoted Pd‐Catalyzed Arylation of Hydrosilanes

The development of novel catalyst systems, especially as highly efficient heterogeneous catalysts for Si‐C bond ‐forming arylation reaction of hydrosilanes is highly desirable. Herein, we developed a simple and eco‐friendly methodology for construction of functionalized phosphorus‐doped porous organic polymers (FPPOPs) and its heterogeneous palladium catalyst through anchoring on FPPOPs bearing a phosphine ligand, in which the fabrication of FPPOPs was completed through the vinyl‐substituted triphenylphosphine (ViPPh3) and vinyl‐substituted polyhedral oligomeric silsequioxane (ViPOSS) as well as functional olefins via radical co‐polymerization. All these FPPOPs could act as a phosphine ligand for Pd‐catalyzed arylation of hydrosilanes have been characterized by SEM, FTIR, and X‐RAD. Moreover, the POSS‐based functionalized phosphorus‐doped porous organic polymers (POSS‐PPOPs) proved to be a high efficiency catalyst system for Si‐C bond ‐forming arylation of hydrosilanes with aryl iodides and with good yields as well as excellent chemoselectivity with low amount of catalyst under mild conditions. The mechanistic studies supported the effect of functional group on the catalytic activity of Pd/FPPOPs catalyst, which revealed that the weak coordination as well as non‐covalent interaction between porous organic polymers and substrate played important role in the enhancement of chemoselectivity.

Sunlight induced C-H arylation of aromatic heterocycles: First example of A3 and A2B type corroles as photoredox catalysts

The visible light mediated metal-free approach has been developed for C–H arylation and borylation employing anilines as starting material. A series of meso-aryl corroles (A3 and A2B type) were synthesized and their catalytic potential was tested in blue light and sunlight. The method includes substituted anilines as source of expensive aryl diazonium salts and utilizes only 0.5 to 1 mol% of corrole catalyst at room temperature. Corrole catalyst worked efficiently under the blue light/sunlight to produce heterobiaryls and aryl boronic esters in decent to good yields (15–80 %). Mechanistic insight was obtained from TD-DFT studies, which suggested single electron transfer (SET) from the singlet state of corrole catalyst to the aryl diazonium salt. The paper demonstrates corrole based photo-redox catalysis as a mild, green and eco-sustainable alternative for the C–H arylation reactions.

Kopplung von Arylchloriden mit Lithium‐Nukleophilen, an molekular definierten Alkynyllithium‐Palladium‐Katalysatoren

AbstractPalladiumkatalysierte Kreuzkupplungen von Arylchloriden erfordern zumeist sterisch anspruchsvolle, elektronenreiche Liganden wie Phosphine oder heterocyclische Carbene. Die Reaktion von Palladiumsalzen mit Alkinyllithium‐Reagenzien liefert jedoch ähnlich leistungsfähige Kreuzkupplungskatalysatoren. Dabei werden zunächst Dilithium‐Tetraalkinylpalladat‐Komplexe gebildet. Diese katalysieren die Kupplung von Arylchloriden mit Lithiumsalzen diverser terminaler Alkine unter Bildung von Alkinylarenen. Isolierte Li‐Alkinyl‐Pd‐Komplexe vermitteln auch Kupplungen von Aryl‐ und Allylchloriden mit (Hetero)aryl‐, Alkyl‐ und Allyllithiumverbindungen sowie mit Lithiumamiden. Keine dieser Reaktionen läuft in Gegenwart unmodifizierter Palladiumsalze ab. Der präparative Nutzen dieses Ansatzes wurde durch die Synthese von 49 Molekülen nachgewiesen, darunter pharmazeutisch relevante Verbindungen.