Day: November 17, 2021

An article Base promoted peroxide systems for the efficient synthesis of nitroarenes and benzamides WOS:000491304300007 published article about ACID-CATALYZED OXIDATION; AROMATIC-AMINES; BENZYLAMINES; AMIDES; CALCIUM in [Gupta, Sampa; Ansari, Alisha; Sashidhara, Koneni V.] CSIR Cent Drug Res Inst, Med & Proc Chem Div, Sect 10,Sitapur Rd, Lucknow 226031, Uttar Pradesh, India; [Ansari, Alisha; Sashidhara, Koneni V.] Acad Sci & Innovat Res, New Delhi 110025, India in 2019.0, Cited 33.0. Formula: C8H7NO3. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

A useful and efficient approach for the synthesis of nitroarenes from several aromatic amines (including heterocycles) using peroxide and base has been developed. This oxidative reaction is very easy to handle and afforded the products in good yields. Formation of benzamides from benzylamine was also successfully carried out with this metal-free catalytic system in good to excellent yields. (C) 2019 Elsevier Ltd. All rights reserved.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Gupta, S; Ansari, A; Sashidhara, KV or concate me.. Formula: C8H7NO3

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Authors Pecak, J; Eder, W; Stoger, B; Realista, S; Martinho, PN; Calhorda, MJ; Linert, W; Kirchner, K in AMER CHEMICAL SOC published article about ORGANOMETALLIC CHEMISTRY; COORDINATION CHEMISTRY; BOND-CLEAVAGE; NITRIC-OXIDE; LIGANDS; PNP; APPROXIMATION; HYDROBORATION; PLATINUM; IRIDIUM in [Pecak, Jan; Eder, Wolfgang; Linert, Wolfgang; Kirchner, Karl] Vienna Univ Technol, Inst Appl Synthet Chem, A-1060 Vienna, Austria; [Stoeger, Berthold] Vienna Univ Technol, Xray Ctr, A-1060 Vienna, Austria; [Realista, Sara] Univ Nova Lisboa, ITQB NOVA, Inst Tecnol Quim & Biol Antonio Xavier, P-2780157 Oeiras, Portugal; [Martinho, Paulo N.; Calhorda, Maria Jose] Univ Lisbon, Fac Ciencias, BioISI Biosyst & Integrat Sci Inst, DQB, P-1749016 Lisbon, Portugal in 2020, Cited 53. HPLC of Formula: C14H11N. The Name is 2,2-Diphenylacetonitrile. Through research, I have a further understanding and discovery of 86-29-3

The reaction of coordinatively unsaturated Co(II) PCP pincer complexes with nitric oxide leads to the formation of new, air-stable, diamagnetic mono nitrosyl compounds. The synthesis and characterization of five- and four-coordinate Co(III) and Co(I) nitrosyl pincer complexes based on three different ligand scaffolds is described. Passing NO through a solution of [Co(PCPNMe-iPr)Cl], [Co(PCPO-iPr)Cl] or [Co(PCPCH2-iPr)Br] led to the formation of the low-spin complex [Co(PCP-iPr)(NO)-X] with a strongly bent NO ligand. Treatment of the latter species with (X = CI, Br) AgBF4 led to chloride abstraction and formation of cationic square-planar Co(I) complexes of the type [Co(PCP-iPr)(NO)](+) featuring a linear NO group. This reaction could be viewed as a formal two electron reduction of the metal center by the NO radical from Co(III) to Co(I), if NO is counted as NO+. Hence, these systems can be described as {CoNO}(8) according to the Enemark-Feltham convention. X-ray structures, spectroscopic and electrochemical data of all nitrosyl complexes are presented. Preliminary studies show that [Co(PCPNMe-iPr)(NO)](+) catalyzes efficiently the reductive hydroboration of nitriles with pinacolborane (HBpin) forming an intermediate {CoNO}(8) hydride species.

About 2,2-Diphenylacetonitrile, If you have any questions, you can contact Pecak, J; Eder, W; Stoger, B; Realista, S; Martinho, PN; Calhorda, MJ; Linert, W; Kirchner, K or concate me.. HPLC of Formula: C14H11N

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Jiang, R; Liu, X; Mu, YX; Iqbal, Z; He, LL; Zhai, LJ; Hou, J; Yang, MH; Yang, ZX; Tang, D in [Jiang, Rui; Mu, Yangxiu; Iqbal, Zafar; He, Lili; Zhai, Lijuan; Hou, Jing; Yang, Zhixiang; Tang, Dong] Ningxia Acad Agr & Forestry Sci, Agr Resource & Environm Inst, Ningxia Ctr Agr Organ Synth, Yinchuan 750002, Ningxia, Peoples R China; [Liu, Xiang] China Three Gorges Univ, Coll Mat & Chem Engn, Yichang 443002, Hubei, Peoples R China; [Yang, Minghua; Tang, Dong] Lishui Univ, Dept Chem, Lishui 323000, Peoples R China published Iron-Catalyzed Synthesis of Polyfunctional Pyridines from Ketoxime Carboxylates and Nitrones in 2020.0, Cited 31.0. COA of Formula: C8H7NO3. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

Polyfunctional pyridines are backbone of numerous natural products and pharmaceutical reactive intermediates. We have developed an iron-catalyzed cyclization reaction between ketoxime carboxylates and nitrones to afford trisubstituted pyridines. Employing this strategy, we have synthesized a number of trisubstituted pyridines with various functional groups in good yields under simple reaction conditions. It is worth mentioning that the nitrones can serve as a novel C1 unit in organic synthesis.

Welcome to talk about 100-19-6, If you have any questions, you can contact Jiang, R; Liu, X; Mu, YX; Iqbal, Z; He, LL; Zhai, LJ; Hou, J; Yang, MH; Yang, ZX; Tang, D or send Email.. COA of Formula: C8H7NO3

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Name: 2,2-Diphenylacetonitrile. Xiang, KR; Tong, P; Yan, BR; Long, LL; Zhao, CB; Zhang, Y; Li, Y in [Xiang, Kuirong; Tong, Pei; Yan, Baorun; Long, Lingling; Zhao, Chunbo; Zhang, Yuan; Li, Ying] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China published Synthesis of Benzannulated [6,6]-Spiroketals by a One-Pot Carbonylative Sonogashira Coupling/Double Annulation Reaction in 2019, Cited 86. The Name is 2,2-Diphenylacetonitrile. Through research, I have a further understanding and discovery of 86-29-3.

A one-pot Pd-catalyzed carbonylative Sonogashira coupling in tandem with double annulation reaction to synthesize benzannulated [6,6]-spiroketals from o-iodophenols and terminal alkynols or alkynyl phenols was achieved. The protocol provides straightforward and facile access to benzannulated [6,6]-spiroketals in moderate to good yields and excellent diastereoselectivities under balloon pressure of CO at room temperature.

Name: 2,2-Diphenylacetonitrile. Bye, fridends, I hope you can learn more about C14H11N, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Authors Tian, M; Liu, XY; He, H; Ma, XZ; Liang, C; Liu, Y; Jiang, FL in AMER CHEMICAL SOC published article about SELECTIVE FLUORESCENT; DESIGN STRATEGIES; SENSOR; CELLS; KINETICS; THIOLS; CANCER in [Tian, Ming; Liu, Xing-Yu; He, Huan; Liu, Yi; Jiang, Feng-Lei] Wuhan Univ, Sauvage Ctr Mol Sci, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China; [Ma, Xian-Zheng; Liang, Chao] Wuhan Univ, Natl Engn Res Ctr Multimedia Software NERCMS, Sch Comp Sci, Wuhan 430072, Peoples R China; [Liu, Yi] Wuhan Univ Sci & Technol, Hubei Prov Key Lab Coal Convers & New Carbon Mat, Sch Chem & Chem Engn, Wuhan 430081, Peoples R China; [Liu, Yi] Nanning Normal Univ, Coll Chem & Mat Sci, Guangxi Key Lab Nat Polymer Chem, Nanning 530001, Peoples R China in 2020.0, Cited 37.0. Name: 1-(4-Nitrophenyl)ethanone. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

Glutathione (GSH), the most abundant nonprotein thiol found in living organisms, are involved in the etiology and progression of many human diseases including cancer. So, monitoring changes of cellular GSH levels has an important guiding significance. To date, however, majority of probes can only qualitatively detect GSH in living cells. Herein, with coumarin as the read-out fluorophore and Michael addition as the sensing mechanism, six fluorescent probes were designed and synthesized. Among them, RP-2 exhibited a reversible and extremely fast response toward GSH (half time: similar to 3 s), which endowed RP2 the capacity of real-time imaging. Among the reversible probes based on Michael addition, RP-2 had both the largest forward and reverse rate constants thus far. The reaction between RP-2 and GSH was studied in detail by density functional theory and fluorescence spectroscopy. Real-time imaging of GSH levels in living cells was achieved with a temporal resolution of seconds. To simplify the processing of images, a program was developed and validated. RP-2 was expected to serve as a new fluorescent imaging tool to understand the function of intracellular GSH in the future.

Name: 1-(4-Nitrophenyl)ethanone. Welcome to talk about 100-19-6, If you have any questions, you can contact Tian, M; Liu, XY; He, H; Ma, XZ; Liang, C; Liu, Y; Jiang, FL or send Email.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Authors Zeng, HS; Wu, J; Li, SH; Hui, C; Ta, A; Cheng, SY; Zheng, SP; Zhang, GQ in AMER CHEMICAL SOC published article about MAGNESIUM-CATALYZED HYDROBORATION; ASYMMETRIC TRANSFER HYDROGENATION; ABUNDANT METAL-CATALYSTS; IRON; ALKYNES; REDUCTION; HYDROSILYLATION; ALKYLATION; MECHANISM; NITRILES in [Zeng, Haisu; Wu, Jing; Li, Sihan; Hui, Christina; Ta, Anita; Cheng, Shu-Yuan; Zhang, Guoqi] CUNY, John Jay Coll, Dept Sci, New York, NY 10019 USA; [Zeng, Haisu; Wu, Jing; Li, Sihan; Hui, Christina; Ta, Anita; Cheng, Shu-Yuan; Zhang, Guoqi] CUNY, Grad Ctr, PhD Program Chem, New York, NY 10019 USA; [Zeng, Haisu; Wu, Jing; Li, Sihan; Zheng, Shengping] CUNY Hunter Coll, Dept Chem, New York, NY 10065 USA in 2019.0, Cited 56.0. Category: benzodioxans. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

A novel nonanuclear copper(II) complex obtained by a facile one-pot self-assembly was found to catalyze the hydroboration of ketones and aldehydes with the absence of an activator under mild, solvent-free conditions. The catalyst is air-and moisture-stable, displaying high efficiency (1980 h(-1) turnover frequency, TOF) and chemo-selectivity on aldehydes over ketones and ketones over imines. This represents a rare example of divalent copper catalyst for the hydroboration of carbonyls.

Welcome to talk about 100-19-6, If you have any questions, you can contact Zeng, HS; Wu, J; Li, SH; Hui, C; Ta, A; Cheng, SY; Zheng, SP; Zhang, GQ or send Email.. Category: benzodioxans

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Authors Mancheno, MJ; Royuela, S; de la Pena, A; Ramos, M; Zamora, F; Segura, JL in AMER CHEMICAL SOC published article about MECHANOCHEMICAL SYNTHESIS; SPECTROSCOPY in [Jose Mancheno, Maria; Royuela, Sergio; de la Pena, A.; Segura, Jose L.] Univ Complutense Madrid, Fac Ciencias Quim, Dept Quim Orgn, E-28040 Madrid, Spain; [Royuela, Sergio; Ramos, Mar] Univ Rey Juan Carlos, Dept Tecnol Quim & Ambiental, Madrid 28933, Spain; [Zamora, Felix] Univ Autonoma Madrid, Fac Ciencias, Dept Quim Inorgan, E-28049 Madrid, Spain in 2019.0, Cited 37.0. Formula: C8H7NO3. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

In order to introduce the concept of covalent organic frameworks (COFs), an important class of predictable crystalline porous polymers, an integrated laboratory experiment for advanced organic chemistry students is reported. The importance of these kind of polymers and their multiple applications are presented as a part of key concepts in polymer and organic chemistry, bridging these disciplines to materials science. Students carry out the synthesis and characterization of an imine-linked COF and its building blocks. The polymer is formed at room temperature by using solvent-assisted synthesis and mechanochemistry. Students are trained in solid state characterization techniques, including FTIR spectroscopy, thermogravimetric analysis (TGA), C-13 NMR cross-polarization-magic angle spinning (CP-MAS) NMR spectroscopy, and powder X-ray diffraction (PXRD), which are essential in the important field of reticular chemistry. Therefore, this lab experience constitutes a practical introduction to COFs.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Mancheno, MJ; Royuela, S; de la Pena, A; Ramos, M; Zamora, F; Segura, JL or concate me.. Formula: C8H7NO3

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

An article Pd supported on graphene modified g-C3N4 hybrid: a highly efficient catalyst for hydrogenation of nitroarenes WOS:000535038100001 published article about GRAPHITIC CARBON NITRIDE; FORMIC-ACID; NANOPARTICLES; NANOSHEETS; REDUCTION; GROWTH; OXIDE; MILD in [Zhang, Longkang; Zhang, Lihong; Cheng, Saisai; Zhou, Xin; Shang, Ningzhao; Gao, Shutao; Wang, Chun] Hebei Agr Univ, Coll Sci, Baoding 071000, Peoples R China in 2020.0, Cited 49.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. HPLC of Formula: C8H7NO3

Graphitic carbon nitride (g-C3N4) and graphene (GO) have been greatly utilized as supports in the field of heterogeneous catalysis. In this work, layered C3N4 polymer/graphene hybrid (CNNS/rGO(20)) with heterostructure was fabricated by a hydrothermal method followed by loading Pd nanoparticles on the hybrid. The palladium was well dispersed uniformly (1.31 nm) owing to the layered and porous heterostructure of CNNS/rGO(20). The obtained catalyst was used for the transfer hydrogenation of a series of nitro-compounds to give the corresponding aromatic amines with outstanding activity by employing formic acid as hydrogen donor under mild conditions. The catalytic activity of the heterogeneous catalyst showed no significant loss after five continuous use.

HPLC of Formula: C8H7NO3. Bye, fridends, I hope you can learn more about C8H7NO3, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

I found the field of Pharmacology & Pharmacy very interesting. Saw the article Design, Synthesis, and Biological Evaluation of Novel Allosteric Protein Disulfide Isomerase Inhibitors published in 2019.0. Product Details of 100-19-6, Reprint Addresses Neamati, N (corresponding author), Univ Michigan, Dept Med Chem, Coll Pharm, Rogel Canc Ctr, North Campus Res Complex,1600 Huron Pkwy, Ann Arbor, MI 48109 USA.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

Protein disulfide isomerase (PDI) is responsible for nascent protein folding in the endoplasmic reticulum (ER) and is critical for glioblastoma survival. To improve the potency of lead PDI inhibitor BAP2 ((E)-3-(3-(4-hydroxyphenyl)-3-oxoprop-1-en-1-yl)benzonitrile), we designed and synthesized 67 analogues. We determined that PDI inhibition relied on the A ring hydroxyl group of the chalcone scaffold and cLogP increase in the sulfonamide chain improved potency. Docking studies revealed that BAP2 and analogues bind to His256 in the b’ domain of PDI, and mutation of His256 to Ala abolishes BAP2 analogue activity. BAP2 and optimized analogue 59 have modest thiol reactivity; however, we propose that PDI inhibition by BAP2 analogues depends on the b’ domain. Importantly, analogues inhibit glioblastoma cell growth, induce ER stress, increase expression of G2M checkpoint proteins, and reduce expression of DNA repair proteins. Cumulatively, our results support inhibition of PDI as a novel strategy to treat glioblastoma.

Welcome to talk about 100-19-6, If you have any questions, you can contact Yang, SH; Shergalis, A; Lu, D; Kyani, A; Liu, ZW; Ljungman, M; Neamati, N or send Email.. Product Details of 100-19-6

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

An article Chiral BrOnsted Acid Catalyzed Dynamic Kinetic Asymmetric Hydroamination of Racemic Allenes and Asymmetric Hydroamination of Dienes WOS:000476423300046 published article about ENANTIOSELECTIVE HYDROAMINATION; METAL CATALYSIS; STEREOCONVERGENT; TRANSFORMATIONS; CLASSIFICATION; ISOMERIZATION; RACEMIZATION; ACTIVATION; S(N)1 in [Lin, Jin-Shun] Tsinghua Univ, Key Lab Chem Biol, State Key Lab Chem Oncogen, Grad Sch Shenzhen, Shenzhen 518055, Peoples R China; [Lin, Jin-Shun] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China; [Lin, Jin-Shun; Li, Tao-Tao; Jiao, Guan-Yuan; Gu, Qiang-Shuai; Cheng, Jiang-Tao; Lv, Ling; Liu, Xin-Yuan] Southern Univ Sci & Technol, Dept Chem, Shenzhen 518055, Peoples R China; [Lin, Jin-Shun; Li, Tao-Tao; Jiao, Guan-Yuan; Cheng, Jiang-Tao; Lv, Ling; Liu, Xin-Yuan] Southern Univ Sci & Technol, Shenzhen Grubbs Inst, Shenzhen 518055, Peoples R China; [Gu, Qiang-Shuai] Southern Univ Sci & Technol, Acad Adv Interdisciplinary Studies, Shenzhen 518055, Peoples R China in 2019, Cited 71. HPLC of Formula: C14H11N. The Name is 2,2-Diphenylacetonitrile. Through research, I have a further understanding and discovery of 86-29-3

The first highly efficient and practical chiral BrOnsted acid catalyzed dynamic kinetic asymmetric hydroamination (DyKAH) of racemic allenes and asymmetric hydroamination of unactivated dienes with both high E/Z selectivity and enantioselectivity are described herein. The transformation proceeds through a new catalytic asymmetric model involving a highly reactive pi-allylic carbocationic intermediate, generated from racemic allenes or dienes through a proton transfer mediated by an activating/directing thiourea group. This method affords expedient access to structurally diverse enantioenriched, potentially bioactive alkenyl-containing aza-heterocycles and bicyclic aza-heterocycles.

About 2,2-Diphenylacetonitrile, If you have any questions, you can contact Lin, JS; Li, TT; Jiao, GY; Gu, QS; Cheng, JT; Lv, L; Liu, XY or concate me.. HPLC of Formula: C14H11N

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem