He, Xiao-Yun et al. published their research in Monatshefte fuer Chemie in 2021 |CAS: 321-28-8

The Article related to haloarene aryltitanium reagent palladium catalyst cross coupling, biaryl preparation, alkyltitanium reagenthaloarene palladium catalyst cross coupling, alkylarene preparation and other aspects.Application of 321-28-8

On July 31, 2021, He, Xiao-Yun published an article.Application of 321-28-8 The title of the article was A general palladium-catalyzed cross-coupling of aryl fluorides and organotitanium (IV) reagents. And the article contained the following:

Pd(OAc)2/1-[2-(di-tert-butylphosphanyl)phenyl]-4-methoxy-piperidine was demonstrated to effectively catalyze cross-coupling of aryl fluoride and aryl(alkyl) titanium reagent. Both electron-deficient and electron-rich aryl fluoride reacted effectively with nucleophile and provided extensive functional groups tolerance. 2-Arylated product was realized by selective activation of the C-F bond. The experimental process involved the reaction of 1-Fluoro-2-methoxybenzene(cas: 321-28-8).Application of 321-28-8

The Article related to haloarene aryltitanium reagent palladium catalyst cross coupling, biaryl preparation, alkyltitanium reagenthaloarene palladium catalyst cross coupling, alkylarene preparation and other aspects.Application of 321-28-8

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Feng, Zihao et al. published their research in Inorganic Chemistry Communications in 2021 |CAS: 91-16-7

The Article related to dimethoxy benzimidazolate zinc metal organic framework preparation crystal structure, chiral photoluminescent dimethoxy benzimidazolate zinc mof preparation crystal structure and other aspects.COA of Formula: C8H10O2

On September 30, 2021, Feng, Zihao; Wu, Canmin; Liao, Wei-Ming; Chung, Lai-Hon; He, Jun published an article.COA of Formula: C8H10O2 The title of the article was Construction and investigation of chiral and photoluminescent Metal-Organic framework based on Zn(II) ions and achiral methoxy-functionalized benzimidazolate linkers. And the article contained the following:

A Zn(II)-based metal-organic framework, namely MeOBim-Zn (1), has been prepared by the reaction between 5,6-dimethoxy-1H-benzo[d]imidazole (MeOBimH) and Zn(NO3)2 in the presence of aqueous ammonia through solvothermal method and characterized by single-crystal x-ray diffraction, TGA and FT-IR. 1 Exhibits a (10,3)-a chiral network constructing from achiral MeOBim- linker and Zn(II) ions via spontaneous resolution In addition, 1 shows photoluminescent emission at 433 nm upon photoexcitation at 365 nm and this emission may originate from dissipation of metal-perturbed 蟺(MeOBim-) to 蟺*(MeOBim-) intraligand (IL) excited state. The experimental process involved the reaction of 1,2-Dimethoxybenzene(cas: 91-16-7).COA of Formula: C8H10O2

The Article related to dimethoxy benzimidazolate zinc metal organic framework preparation crystal structure, chiral photoluminescent dimethoxy benzimidazolate zinc mof preparation crystal structure and other aspects.COA of Formula: C8H10O2

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Shi, Weimin et al. published their research in Chemistry – A European Journal in 2020 |CAS: 321-28-8

The Article related to aryl fluoride aliphatic amine photoredox catalyst nucleophilic aromatic substitution, amines, aryl fluorides, nucleophilic aromatic substitution, visible-light photocatalysis and other aspects.Related Products of 321-28-8

On November 25, 2020, Shi, Weimin; Zhang, Jingjie; Zhao, Fengqian; Wei, Wei; Liang, Fang; Zhang, Yin; Zhou, Shaolin published an article.Related Products of 321-28-8 The title of the article was Nucleophilic Aromatic Substitution of Unactivated Aryl Fluorides with Primary Aliphatic Amines by Organic Photoredox Catalysis. And the article contained the following:

A mild and transition-metal-free approach for the nucleophilic aromatic substitution (SNAr) of unactivated fluoroarenes with primary aliphatic amines to form aromatic amines was reported. This reaction is facilitated by the formation of cationic fluoroarene radical intermediates in the presence of an acridinium-based organic photocatalyst under blue-light irradiation Various electron-rich and electron-neutral fluoroarenes are competent electrophiles for this transformation. A wide range of primary aliphatic amines, including amino acid esters, dipeptides and linear and branched amines are suitable nucleophiles. The synthetic utility of this protocol is demonstrated by the late-stage functionalization of several complex drug mols. The experimental process involved the reaction of 1-Fluoro-2-methoxybenzene(cas: 321-28-8).Related Products of 321-28-8

The Article related to aryl fluoride aliphatic amine photoredox catalyst nucleophilic aromatic substitution, amines, aryl fluorides, nucleophilic aromatic substitution, visible-light photocatalysis and other aspects.Related Products of 321-28-8

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Wang, Dinghui et al. published their research in Molecules in 2022 |CAS: 150-78-7

The Article related to pillararene anthracene conjugated polymer morphol optical property, conjugated polymer, host鈥揼uest interaction, light-emitting materials, pillararene, supramolecular chemistry and other aspects.Reference of 1,4-Dimethoxybenzene

Wang, Dinghui; Wang, Jun; Wang, Yan; Yang, Yingwei published an article in 2022, the title of the article was A Fluorescent Linear Conjugated Polymer Constructed from Pillararene and Anthracene.Reference of 1,4-Dimethoxybenzene And the article contains the following content:

Over the past few years, conjugated polymers (CPs) have aroused much attention owing to their rigid conjugated structures, which can perform well in light harvesting and energy transfer and offer great potential in materials chem. In this article, we fabricate a new luminescent linear CP p(P[5](OTf)2-co-9,10-dea) via the Sonogashira coupling of 9,10-diethynylanthracene and trifluoromethanesulfonic anhydride (OTf) modified pillar[5]arene, generating enhanced yellow-green fluorescence emission at around 552 nm. The reaction condition was screened to get a deeper understanding of this polymerization approach, resulting in an excellent yield as high as 92% ultimately. Besides the optical properties, self-assembly behaviors of the CP in low/high concentrations were studied, where interesting adjustable morphologies from tube to sheet were observed In addition, the fluorescence performance and structural architecture can be disturbed by the host-guest reorganization between the host CP and the guest adiponitrile, suggesting great potential of this CP material in the field of sensing and detection. The experimental process involved the reaction of 1,4-Dimethoxybenzene(cas: 150-78-7).Reference of 1,4-Dimethoxybenzene

The Article related to pillararene anthracene conjugated polymer morphol optical property, conjugated polymer, host鈥揼uest interaction, light-emitting materials, pillararene, supramolecular chemistry and other aspects.Reference of 1,4-Dimethoxybenzene

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Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Xia, Xiao-Feng et al. published their research in Advanced Synthesis & Catalysis in 2019 |CAS: 157869-15-3

The Article related to carbonylquinoline preparation green chem metal free, enyne tandem intramol radical cyclization oxygen insertion, aminoalkyne alkenylaniline michael addition radical annulation and other aspects.Product Details of 157869-15-3

Xia, Xiao-Feng; He, Wei; Wang, Dawei published an article in 2019, the title of the article was Metal-Free Oxidative Annulation/Cyclization of 1,6-Enynes for the Synthesis of 4-Carbonylquinolines.Product Details of 157869-15-3 And the article contains the following content:

Herein, the development of a metal-free oxidative annulation reaction of 1,6-enynes, leading to 4-carbonylquinolines by using dioxygen as a green sustainable oxidant is reported. Key advances include the use of readily available tert-Bu nitrite (TBN) to promote radical annulation of 1,6-enynes and easy-to-handle reaction conditions. Preliminary mechanistic studies including radical capture reactions and isotope labeling experiments are also conducted. The experimental process involved the reaction of 2-((4-Methoxyphenyl)ethynyl)aniline(cas: 157869-15-3).Product Details of 157869-15-3

The Article related to carbonylquinoline preparation green chem metal free, enyne tandem intramol radical cyclization oxygen insertion, aminoalkyne alkenylaniline michael addition radical annulation and other aspects.Product Details of 157869-15-3

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Elacqua, Elizabeth et al. published their research in Angewandte Chemie, International Edition in 2019 |CAS: 146370-51-6

The Article related to paracyclophane ring opening metathesis polymerization polyarylenevinylene block copolymer, metathesis, paracyclophanes, polymers, ring-opening polymerization, stereoelectronics and other aspects.Recommanded Product: 146370-51-6

Elacqua, Elizabeth; Gregor, Maria published an article in 2019, the title of the article was Poly(arylenevinylene)s through Ring-Opening Metathesis Polymerization of an Unsymmetrical Donor-Acceptor Cyclophane.Recommanded Product: 146370-51-6 And the article contains the following content:

Reported are well-defined donor-acceptor alternating copolymers prepared using ring-opening metathesis polymerization (ROMP). Unsym. cyclophanedienes comprising electron-donating (4-methoxy-1-(2-ethylhexyl)oxy)benzene (MEH) and electron-accepting benzothiadiazole (BT) rings were synthesized from the corresponding [3.3]dithiaparacyclophanes. ROMP of the strained unsym. and “electronically-ambiguous” cyclophanedienes proceeded in a controlled manner in the presence of either Hoveyda-Grubbs II or Grubbs II initiator in wake of both steric and electronic encumbrance. The resulting polymers, comprising alternating BT and MEH-PPV units, are achieved in mol. weights exceeding 20k with D values ranging from 1.1-1.4. The living nature of the polymerization is verified through the formation of rod-coil and rod-rod block copolymers. Our strategy to develop previously unrealized polymers from functional building blocks featuring a locked-in D-A unit is significant in a field striving to achieve well-defined and sequence-specific materials. The experimental process involved the reaction of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene(cas: 146370-51-6).Recommanded Product: 146370-51-6

The Article related to paracyclophane ring opening metathesis polymerization polyarylenevinylene block copolymer, metathesis, paracyclophanes, polymers, ring-opening polymerization, stereoelectronics and other aspects.Recommanded Product: 146370-51-6

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Mao, Xiaowei et al. published their research in ACS Applied Bio Materials in 2021 |CAS: 150-78-7

The Article related to naphthylmethyl triazolylmethyl pillararene go preparation hela cell adhesion separation, arginine, cell adhesion behavior, graphene oxide, host鈭抔uest chemistry, pillar[5]arenes and other aspects.Electric Literature of 150-78-7

On September 20, 2021, Mao, Xiaowei; Cheng, Ming; Chen, Linfeng; Cheng, Jing; Li, Haibing published an article.Electric Literature of 150-78-7 The title of the article was Host-Guest Chemistry Triggered Differential HeLa Cell Behavior Based on Pillar[5]arene-Modified Graphene Oxide Surfaces. And the article contained the following:

The regulation of surface wettability and cell adhesion behavior in a mild and unperturbed state at the interface remains a challenging task. To address this task, we adopt a strategy, based on bridging the host-guest recognition capacities of pillar[5]arene and good attachment for cell adhesion abilities of graphene oxide, to construct a smart pillar[5]arene triazole-linked naphthalene-modified graphene oxide interface. The hybrid surface exhibited a good stimuli-responsive selectivity toward arginine, as demonstrated by the wettability and cell adhesion behavior. Further studies at mol. levels indicated that the recognition mechanism of arginine was probably due to the formation of a host-guest complex driven by 蟺-蟺 stacking interactions between the cavity of pillar[5]arenes and arginine, which eventually resulted in the change in surface wettability and cellular adhesion behavior. It not only signifies a host-guest interaction strategy for the design of smart devices via the host-guest effect but also inspires the design of high-performance biointerface for affinity-adherent cells without exposing cells to harsh phys. and chem. conditions. The experimental process involved the reaction of 1,4-Dimethoxybenzene(cas: 150-78-7).Electric Literature of 150-78-7

The Article related to naphthylmethyl triazolylmethyl pillararene go preparation hela cell adhesion separation, arginine, cell adhesion behavior, graphene oxide, host鈭抔uest chemistry, pillar[5]arenes and other aspects.Electric Literature of 150-78-7

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Liu, Xiang-Wie et al. published their research in Angewandte Chemie, International Edition in 2019 |CAS: 321-28-8

The Article related to base mediated defluorosilylation unactivated carbon fluorine bond aryl fluoride, silane preparation, cross-coupling, fluorine, reaction mechanisms, silylation, synthetic methods and other aspects.Synthetic Route of 321-28-8

Liu, Xiang-Wie; Zarate, Cayetana; Martin, Ruben published an article in 2019, the title of the article was Base-Mediated Defluorosilylation of C(sp2)-F and C(sp3)-F Bonds.Synthetic Route of 321-28-8 And the article contains the following content:

The ability to selectively forge C-heteroatom bonds by C-F scission is typically accomplished by metal catalysts, specialized ligands and/or harsh reaction conditions. Described herein is a base-mediated defluorosilylation of unactivated C(sp2)-F and C(sp3)-F bonds that obviates the need for metal catalysts. This protocol was characterized by its simplicity, mild reaction conditions, and wide scope, even within the context of late-stage functionalization, constituting a complementary approach to existing C-Si bond-forming protocols. The experimental process involved the reaction of 1-Fluoro-2-methoxybenzene(cas: 321-28-8).Synthetic Route of 321-28-8

The Article related to base mediated defluorosilylation unactivated carbon fluorine bond aryl fluoride, silane preparation, cross-coupling, fluorine, reaction mechanisms, silylation, synthetic methods and other aspects.Synthetic Route of 321-28-8

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Otani, Takashi et al. published their research in Advanced Synthesis & Catalysis in 2015 |CAS: 157869-15-3

The Article related to indole imidoyl quinazoline dihydro alkylidene preparation diastereoselective regioselective, aniline alkynyl imidoyl cycloisomerization silver triflate catalyst cyclization tbaf and other aspects.SDS of cas: 157869-15-3

Otani, Takashi; Jiang, Xue; Cho, Kinryo; Araki, Rino; Kutsumura, Noriki; Saito, Takao published an article in 2015, the title of the article was Lewis Acid-Catalyzed or Base-Promoted Regioselective Cycloisomerization of N-Imidoyl-o-alkynylanilines for Synthesis of N-Imidoyl-(1H)-indoles and 4-Alkylidene-3,4-dihydroquinazolines.SDS of cas: 157869-15-3 And the article contains the following content:

The product selectivity control for the synthesis of imidoylindoles I (R1 = 4-Tol, Ph, t-Bu, n-Pr, etc; R2 = Ph, n-Pr, i-Pr; R3 = Ph, Et) and 4-alkylidenedihydroquinazolines II (R4 = 4-CH3OC6H4, 4-F3CC6H4, cyclohexyl, etc; R5 = Ph, n-Pr, i-Pr, t-Bu) from N-imidoyl-o-alkynylanilines via silver triflate-catalyzed cycloisomerization or tetrabutylammonium fluoride-promoted cyclization were described. The product selectivity depends mainly on the catalyst/promoter used, and on the substituents on the alkyne and amidine functions of the substrates. The experimental process involved the reaction of 2-((4-Methoxyphenyl)ethynyl)aniline(cas: 157869-15-3).SDS of cas: 157869-15-3

The Article related to indole imidoyl quinazoline dihydro alkylidene preparation diastereoselective regioselective, aniline alkynyl imidoyl cycloisomerization silver triflate catalyst cyclization tbaf and other aspects.SDS of cas: 157869-15-3

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Yu, Jianfei et al. published their research in Organic Letters in 2022 |CAS: 81616-80-0

The Article related to propanoic acid preparation enantioselective, acrylic acid hydrogenation chiral diphosphine ferrocene catalyst, sym chiral ferrocene diphosphinoethane ligand preparation catalyst and other aspects.Computed Properties of 81616-80-0

On April 15, 2022, Yu, Jianfei; Zhu, Haowei; Zhang, Xumu; Chen, Gen-Qiang published an article.Computed Properties of 81616-80-0 The title of the article was Development of C2-Symmetric Chiral Diphosphine Ligands for Highly Enantioselective Hydrogenation Assisted by Ion Pairing. And the article contained the following:

A new series of C2-sym. chiral ferrocene-based diphosphino-ethane ligands termed as f-DPE, I (R = Ph, Me CH2Ph, 2-MeOC6H4, 3-MeOC6H4, 4-MeOC6H4) were developed. Assisted by the ion pairing interaction with the ligand, a wide scope of 2-substituted acrylic acids was hydrogenated to obtain chiral propanoic acids. with high yields and enantioselectivities. The well-known anti-inflammatory drugs ibuprofen, naproxen, and flurbiprofen could be synthesized efficiently. In addition, the synthetic utilities of the current method were demonstrated by gram-scale experiments The experimental process involved the reaction of (S)-2-(2-Methoxyphenyl)propanoic acid(cas: 81616-80-0).Computed Properties of 81616-80-0

The Article related to propanoic acid preparation enantioselective, acrylic acid hydrogenation chiral diphosphine ferrocene catalyst, sym chiral ferrocene diphosphinoethane ligand preparation catalyst and other aspects.Computed Properties of 81616-80-0

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem