Category: 93-04-9

Deng, Jiazhu published the artcilePreparation of a cost-effective Ni-Ag bimetallic catalyst for hydrodehalogenation of aryl halides under mild conditions, Recommanded Product: 2-Methoxynaphthalene, the publication is New Journal of Chemistry (2022), 46(25), 12169-12176, database is CAplus.

Cost-effective Ni-Ag bimetallic nanoparticles were prepared using an aqueous-phase surfactant-aided co-reduction process and used as catalysts for the hydrodehalogenation of aryl halides CAr-X (X = F, Cl, Br). CAr-X could be easily converted at 60°C by using water as a solvent, with a CAr-H yield higher than 90%. This catalyst was widely applicable in the hydrodehalogenation of halogenated aromatics with various functional groups (more than 40 examples), including the high concentration solution of aryl fluorides, polyhalogenated phenol, environmental pollutants like 2,4-dichlorophenoxyacetic acid (2,4-D) and triclosan. Furthermore, it could be easily recycled and reused, providing a green and cost-effective method for the degradation of polyhalogenated aromatic pollutants and synthesis of important structural units through hydrodehalogenation reactions.

New Journal of Chemistry published new progress about 93-04-9. 93-04-9 belongs to ethers-buliding-blocks, auxiliary class Naphthalene,Ether, name is 2-Methoxynaphthalene, and the molecular formula is C11H10O, Recommanded Product: 2-Methoxynaphthalene.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Baker, Sarah I. published the artcileEnhanced Reactivity for Aromatic Bromination via Halogen Bonding with Lactic Acid Derivatives, HPLC of Formula: 93-04-9, the publication is Journal of Organic Chemistry (2022), 87(13), 8492-8502, database is CAplus and MEDLINE.

Herein, a new method for regioselective aromatic bromination using lactic acid derivatives as halogen bond acceptors with N-bromosuccinimide (NBS) is reported. Several structural analogs of lactic acid affected the efficiency of aromatic brominations, presumably via Lewis acid/base halogen-bonding interactions. Rate comparisons of aromatic brominations demonstrated the reactivity enhancement available via catalytic additives capable of halogen bonding. Computational results demonstrated that Lewis basic additives interact with NBS to increase the electropos. character of bromine prior to electrophilic transfer. An optimized procedure using catalytic mandelic acid under aqueous conditions at room temperature has been developed to promote aromatic bromination on a variety of arene substrates with complete regioselectivity.

Journal of Organic Chemistry published new progress about 93-04-9. 93-04-9 belongs to ethers-buliding-blocks, auxiliary class Naphthalene,Ether, name is 2-Methoxynaphthalene, and the molecular formula is C11H10O, HPLC of Formula: 93-04-9.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Gao, Yang published the artcilePractical synthesis of 3-aryl anthranils via an electrophilic aromatic substitution strategy, Formula: C11H10O, the publication is Chemical Science (2022), 13(7), 2105-2114, database is CAplus and MEDLINE.

A practical route for the synthesis of valuable 3-aryl anthranils from readily available anthranils and simple arenes by using the classical electrophilic aromatic substitution (EAS) strategy was reported. This transformation goes through an electrophilic substitution and rearomatisation sequence by employing Tf₂O as an effective activator. A wide range of arenes were compatible in this transformation, delivering various structurally diversified 3-aryl anthranils in good yields and high regioselectivity. In addition, a variety of readily available feedstocks such as olefins, alkenyl triflates, silyl enolethers, carbonyl compounds, thiophenols and thiols could also participate in the reaction to achieve the C3 alkenylation, alkylation and thioetherification of anthranils. Of note, the synthesized 3-aryl anthranils proved to be a highly robust platform to access a series of biol. active compounds, drug derivatives and organic optoelectronic materials.

Chemical Science published new progress about 93-04-9. 93-04-9 belongs to ethers-buliding-blocks, auxiliary class Naphthalene,Ether, name is 2-Methoxynaphthalene, and the molecular formula is C11H10O, Formula: C11H10O.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Dong, Wenbo published the artcileA highly stable all-in-one photocatalyst for aryl etherification: the Ni^II embedded covalent organic framework, Name: 2-Methoxynaphthalene, the publication is Green Chemistry (2021), 23(16), 5797-5805, database is CAplus.

The efficient conversion of aryl bromides to the corresponding aryl alkyl ethers by dual Ni/photocatalysis has seen great progress, but difficulties of recycling the photosensitizer or Ni complexes cause problems of sustainability. Here, the authors report the design of a novel, highly stable vinyl bridge 2-dimensional covalent organic framework (COF) containing Ni, which combines the role of photosensitizer and reactive site. The as-prepared sp²c-COF_dpy-Ni acts as an efficient heterogeneous photocatalyst for C-O cross coupling. The sp²c-COF_dpy-Ni can be completely recovered and used repeatedly without loss of activity, overcoming the limitations of the prior methods. Preliminary studies reveal that strong interlayer electron transfer may facilitate the generation of the proposed intermediate sp²c-COF_dpy-Ni^I in a bimol. and self-sustained manner. This all-in-one heterogeneous photocatalyst exhibits good compatibility of substrates and tolerance of functional groups. The successful attempt to expand the 2-dimensional COFs with this new catalyst into photocatalytic organic transformation opens an avenue for photoredox/transition metal mediated coupling reactions.

Green Chemistry published new progress about 93-04-9. 93-04-9 belongs to ethers-buliding-blocks, auxiliary class Naphthalene,Ether, name is 2-Methoxynaphthalene, and the molecular formula is C11H10O, Name: 2-Methoxynaphthalene.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Peng, Bing published the artcilePhotodegradation of naproxen using CuZnAl-layered double hydroxides as photocatalysts, Application In Synthesis of 93-04-9, the publication is CrystEngComm (2022), 24(28), 5080-5089, database is CAplus.

Naproxen (NPX), as a typical pharmaceutical and personal care product (PPCP), is frequently detected in water and is difficult to remove effectively by conventional methods. Layered double hydroxides, as highly efficient photocatalysts, have not been used in photocatalysis of PPCP. In this study, CuZnAl-layered double hydroxide (CuZnAl-LDH) was prepared and its performance in the photocatalytic degradation of NPX under UV light illumination was investigated. The results indicated that the NPX photodegradation is considerably enhanced by CuZnAl-LDH with an efficiency of 98.25% in the optimal conditions, which was obviously more than that under pure light condition (efficiency less than 30%). In addition, the CuZnAl-LDH photocatalyst exhibited superior photocatalytic stability confirmed by the analyses of the catalyst structure, morphol., and cycle experiments Moreover, by the comparison of optical properties of ZnAl-LDH and CuZnAl-LDH, it was found that Cu²⁺ can broaden light absorption and facilitate the separation of photogenerated charges electrons (e^–) and holes (h⁺), and in the CuZnAl-LDH system, the formation mechanism of active species complies with the mechanisms of the ligand-to-metal charge transfer (LMCT) from the 2p orbital of oxygen to the 3d orbital of M²⁺ and of the d-d transition of Cu²⁺ ions of the CuO₆ unit. Besides, ESR and scavenging tests revealed that the photocatalytic process was enhanced by the synergistic effect of h⁺, O₂^–, and OH, which displayed the sequence of h⁺ > ^.O₂^– > ^.OH. Finally, the intermediate products were identified by LCMS-IT-TOF, and no intermediates with greater toxicity than NPX were produced. The possible degradation pathway of NPX was proposed involving the decarboxylation, demethylation, and hydroxylation reactions and ring-opening based on intermediates. These results are expected to provide new data on the photodegradation of naproxen.

CrystEngComm published new progress about 93-04-9. 93-04-9 belongs to ethers-buliding-blocks, auxiliary class Naphthalene,Ether, name is 2-Methoxynaphthalene, and the molecular formula is C11H10O, Application In Synthesis of 93-04-9.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Lu, Qixing published the artcileC-H heteroarylation of aromatics via catalyst free S_N2′ coupling cycloaromatization, HPLC of Formula: 93-04-9, the publication is Green Chemistry (2022), 24(11), 4399-4404, database is CAplus.

The construction of a carbon-carbon bond is the most fundamental aspect of synthetic chem. In this study, authors developed a catalyst-free S_N2′ reaction of β-OTf-substituted enamides with aromatics to obtain aryl-substituted aza-1,4-dicarbonyl compounds that can be in situ transformed into aryl-imidazole, aryl-thiazole, and aryl-oxazole in one-pot operation, thus achieving C-H heteroarylation of aromatics This simple, efficient, clean and scalable strategy, which provides difficult-to-realize biaryl products, is compatible with various aromatics having varying complexities. This method can be used for the late-stage modification of various com. pharmaceuticals or functional materials and offers an orthogonal approach for constructing biaryl compounds

Green Chemistry published new progress about 93-04-9. 93-04-9 belongs to ethers-buliding-blocks, auxiliary class Naphthalene,Ether, name is 2-Methoxynaphthalene, and the molecular formula is C11H10O, HPLC of Formula: 93-04-9.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Li, Yonglong published the artcileTunable Photocatalytic Two-Electron Shuttle between Paired Redox Sites on Halide Perovskite Nanocrystals, Recommanded Product: 2-Methoxynaphthalene, the publication is ACS Catalysis (2022), 12(10), 5903-5910, database is CAplus.

Perovskite semiconductors as advanced solar energy-converting materials are promising catalysts for photoredox organic synthesis. Despite the high concentration of charge carriers generated on the perovskite surface, efficient utilization of these nonequilibrium and shambolic energetic carriers to trigger a chem. reaction remains a hot and challenging subject. Here, we report a photon-mediated electron shuttle between paired redox sites on perovskite nanocrystals for the reformation of highly stable carbon-halogen bonds, where both surface electrons and holes are utilized simultaneously. The photo-redox cascade can be effortlessly tailored by precise control of the surface-reducing/-oxidizing reaction rates, which unlocks the transformation for a wide range of (het)arenes. This work demonstrates colloidal perovskite photocatalysts for the direct installation of more than 10 different synthetically important functional groups onto arenes and heteroarenes.

ACS Catalysis published new progress about 93-04-9. 93-04-9 belongs to ethers-buliding-blocks, auxiliary class Naphthalene,Ether, name is 2-Methoxynaphthalene, and the molecular formula is C11H10O, Recommanded Product: 2-Methoxynaphthalene.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Xu, Ren-Rui published the artcilePalladium-catalyzed cascade Heck-type thiocarbonylation for the synthesis of functionalized thioesters, Safety of 2-Methoxynaphthalene, the publication is Organic Chemistry Frontiers (2022), 9(5), 1417-1421, database is CAplus.

A palladium-catalyzed cascade Heck-type cyclization and carbonylation reaction has been developed for the synthesis of functionalized thioesters. With arylsulfonyl chlorides as odorless and readily available sulfur sources, a variety of thioesters were obtained in moderate to good yields with good functional group compatibility. In this system, Mo(CO)₆ acts as both a convenient CO surrogate and a suitable reductant.

Organic Chemistry Frontiers published new progress about 93-04-9. 93-04-9 belongs to ethers-buliding-blocks, auxiliary class Naphthalene,Ether, name is 2-Methoxynaphthalene, and the molecular formula is C8H8O3, Safety of 2-Methoxynaphthalene.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Zhang, Hongliang published the artcileElectrophilic amidomethylation of arenes with DMSO/MeCN reagents, Related Products of ethers-buliding-blocks, the publication is Organic Chemistry Frontiers (2022), 9(9), 2430-2437, database is CAplus.

An efficient electrophilic amidomethylation of aromatics was described to construct N-benzylic amides, which are core structures in drugs and natural products. The simple combination of DMSO (DMSO, as the CH₂ unit) and acetonitrile (MeCN, as the nitrogen unit) as a highly active amidomethylation reagent enables the efficient C-C, C-N and C=O bond construction. Notably, this method provides a practical protocol for the efficient preparation of deuterated benzylamine derivatives with easily available d₆-DMSO or d₃-MeCN, and is also applied in the concise synthesis of Nonivamide and Pimavanserin.

Organic Chemistry Frontiers published new progress about 93-04-9. 93-04-9 belongs to ethers-buliding-blocks, auxiliary class Naphthalene,Ether, name is 2-Methoxynaphthalene, and the molecular formula is C15H24S, Related Products of ethers-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

He, Xinxin published the artcileBis-selenonium Cations as Bidentate Chalcogen Bond Donors in Catalysis, Safety of 2-Methoxynaphthalene, the publication is ACS Catalysis (2021), 11(20), 12632-12642, database is CAplus.

Hydrolytically stable bidentate Lewis acid catalysts derived from selenonium dicationic centers were developed. The bis-selenonium catalysts were employed in the activation of imine and carbonyl groups in various transformations with good yields and selectivity. Lewis acidity of the bis-selenonium salts was found to be stronger than that of the monoselenonium systems, attributed to the synergistic effect of the two cationic selenonium centers. In addition, the bis-selenonium catalysts were not inhibited by strong bases or moisture.

ACS Catalysis published new progress about 93-04-9. 93-04-9 belongs to ethers-buliding-blocks, auxiliary class Naphthalene,Ether, name is 2-Methoxynaphthalene, and the molecular formula is C11H10O, Safety of 2-Methoxynaphthalene.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem