Category: 119-61-9

An article Base-Catalyzed [3+2] Cycloaddition of N-Benzyl Ketimines to Arylacetylenes Followed by Oxidation: A One-Pot Access to Polyarylated 2H-Pyrroles via Intermediate Pyrrolines WOS:000661126700008 published article about 2-ACETYL-1-PYRROLINE; DEAROMATIZATION; ACETYLENES; VINYLATION; ALKALOIDS; CHEMISTRY; SUPERBASE; MYOSMINE; WATER in [Bidusenko, Ivan A.; Schmidt, Elena Yu; Ushakov, Igor A.; Vashchenko, Alexander V.; Trofimov, Boris A.] Russian Acad Sci, AE Favorsky Irkutsk Inst Chem, Siberian Branch, Irkutsk 664033, Russia in 2021.0, Cited 38.0. HPLC of Formula: C13H10O. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

N-Benzyl ketimines undergo [3 + 2] cycloaddition with arylacetylenes in the KOBut/DMSO solution to 2,3,5-triarylpyrrolines, which are oxidized (chloranil, DDQ) in situ to 2,3,5-triaryl-2H-pyrroles in 53-71% yields. The intermediate 1-pyrrolines can be isolated in 31-91% yields and separately oxidized to the corresponding 2H-pyrroles.

HPLC of Formula: C13H10O. Welcome to talk about 119-61-9, If you have any questions, you can contact Bidusenko, IA; Schmidt, EY; Ushakov, IA; Vashchenko, AV; Trofimov, BA or send Email.

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Thiomorpholine – Wikipedia,
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SDS of cas: 119-61-9. Authors Liu, SH; Brunel, D; Noirbent, G; Mau, A; Chen, H; Morlet-Savary, F; Graff, B; Gigmes, D; Xiao, P; Dumur, F; Lalevee, J in ROYAL SOC CHEMISTRY published article about in [Liu, Shaohui; Mau, Alexandre; Chen, Hong; Morlet-Savary, Fabrice; Graff, Bernadette; Lalevee, Jacques] Univ Haute Alsace, CNRS, IS2M, UMR 7361, F-68100 Mulhouse, France; [Liu, Shaohui; Mau, Alexandre; Chen, Hong; Morlet-Savary, Fabrice; Graff, Bernadette; Lalevee, Jacques] Univ Strasbourg, Strasbourg, France; [Brunel, Damien; Noirbent, Guillaume; Gigmes, Didier; Dumur, Frederic] Aix Marseille Univ, CNRS, ICR, UMR 7273, F-13397 Marseille, France; [Xiao, Pu] Australian Natl Univ, Res Sch Chem, Canberra, ACT 2601, Australia in 2021.0, Cited 29.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

In this paper, seven new photoinitiators based on the benzophenone scaffold are specifically designed for photopolymerization under mild conditions upon light-emitting diode (LED) irradiation, i.e. four benzophenone-triphenylamine photoinitiators (denoted as BT1-BT4) and three benzophenone-carbazole photoinitiators (denoted as BC1-BC3). Noticeably, these structures have never been reported in the literature except for BT4, so these molecules have been specifically designed for photopolymerization applications. Remarkably, various combinations of chemical groups were investigated in this work to determine the effects of the substitution patterns on their photoinitiation abilities. The formation of benzophenone-triphenylamine and benzophenone-carbazole hybrid structures not only contributes to red-shift of the absorption maxima but also strongly enhances their molar extinction coefficients. The different compounds showed high photoinitiation abilities upon irradiation with an LED@405 nm, and the free radical photopolymerization of acrylates and the cationic polymerization of epoxides could be promoted with high final function conversions (e.g. 77% for the BT3/iodonium salt/amine system in free radical photopolymerization). Remarkably, these new PIs are also able to sensitize sulfonium salts upon irradiation @405 nm. Markedly, because of the benzophenone moiety, a monocomponent Type II PI behavior could be observed, e.g. these compounds could initiate the polymerization alone. Remarkably, benzophenone-triphenylamine compounds BT2, BT3 and BT4 exhibited better hydrogen abstraction abilities as Type II photoinitiators than the benchmark and commercial photoinitiator 2-isopropylthioxanthone in the absence of amines as well as in the presence of amines. Furthermore, the interaction between the photoinitiators and the different additives was investigated by steady state photolysis and fluorescence quenching experiments. The free radical generation in the BT3/amine system was confirmed by the electron spin resonance-spin trapping technique, and the chemical mechanisms related to the polymerization efficiency are discussed. In addition, the migration stability of BT3 was investigated, which was excellent due to its high molecular weight and its trifunctional character. Finally, the three-component photoinitiating system based on BT3 was successfully applied in 3D printing and the 3D patterns showed a good spatial resolution.

SDS of cas: 119-61-9. Welcome to talk about 119-61-9, If you have any questions, you can contact Liu, SH; Brunel, D; Noirbent, G; Mau, A; Chen, H; Morlet-Savary, F; Graff, B; Gigmes, D; Xiao, P; Dumur, F; Lalevee, J or send Email.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Category: thiomorpholine. Authors Li, XS; Xu, DT; Niu, ZJ; Li, M; Shi, WY; Wang, CT; Wei, WX; Liang, YM in AMER CHEMICAL SOC published article about in [Li, Xue-Song; Xu, Dan-Tong; Niu, Zhi-Jie; Li, Ming; Shi, Wei-Yu; Wang, Cui-Tian; Wei, Wan-Xu; Liang, Yong-Min] Lanzhou Univ, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China in 2021.0, Cited 53.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

A gold-catalyzed tandem annulation of propargylic alcohols and pyridylhomopropargylic alcohols is achieved, providing an atom-economical approach to a diverse set of polycyclic dihydrobenzofurans in good yields. The reaction proceeds via the 5-endo-dig cyclization/Meyer-Schuster rearrangement/Friedel-Crafts-type pathway. In this way, three C-C bonds and one C-O bond form to give a polycyclic skeleton in a one-pot process. Moreover, the products exhibit unique optical properties, which reveal their potential application value.

Category: thiomorpholine. Bye, fridends, I hope you can learn more about C13H10O, If you have any questions, you can browse other blog as well. See you lster.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Recently I am researching about RADICAL CYCLIZATION; ALKYL RADICALS; GENERATION; ANNULATION, Saw an article supported by the BMBFFederal Ministry of Education & Research (BMBF) [16GW0202]. SDS of cas: 119-61-9. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Schulz, G; Kirschning, A. The CAS is 119-61-9. Through research, I have a further understanding and discovery of Benzophenone

The smooth oxidative radical decarboxylation of carboxylic acids with TEMPO and other derivatives as radical scavengers is reported. The key to success was the use of a two-phase solvent system to avoid otherwise predominant side reactions such as the oxidation of TEMPO by persulfate and enabled the selective formation of synthetically useful alkoxyamines. The method does not require transition metals and was successfully used in a new synthetic approach for the antidepressant indatraline.

Welcome to talk about 119-61-9, If you have any questions, you can contact Schulz, G; Kirschning, A or send Email.. SDS of cas: 119-61-9

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Formula: C13H10O. Authors Park, N; Jeon, J in PERGAMON-ELSEVIER SCIENCE LTD published article about in [Park, Naree; Jeon, Junho] Changwon Natl Univ, Grad Sch FEED Ecofriendly Offshore Struct, Chang Won 51140, Gyeongsangnamdo, South Korea; [Jeon, Junho] Changwon Natl Univ, Sch Civil Environm & Chem Engn, Chang Won 51140, Gyeongsangnamdo, South Korea; [Jeon, Junho] Changwon Natl Univ, Dept Smart Ocean Environm Energy, Chang Won 51140, Gyeongsangnamdo, South Korea in 2021.0, Cited 68.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

The extensive development and use of new anthropogenic chemicals have inevitably led to their presence in aquatic environments. Surface waters affected by sewage effluents have been exposed to these new substances. In the present study, the occurrence of anthropogenic substances, including pharmaceuticals and industrial chemicals, was investigated in one of the major rivers in Korea, the Nakdong River. Furthermore, seasonal variations in their content were determined via annual monitoring. Through the suspect and non-target screening (SNTS) technique, 58 substances were newly identified in the river and integrated in the quantitative monitoring practice. The results revealed that niflumic acid and melamine exhibited the highest median concentrations, i.e., 320 ng/L and 11,000 ng/L, respectively. The results associated with seasonal change revealed that the concentration of a considerable number of substances increased in winter when the flow rate was low. Conversely, some substances exhibited high concentrations in summer (e.g., polyethylene glycol) and spring (e.g., niflumic acid). This was attributed to the seasonal changes in the consumption, prescriptions, or the application of alternative substances. These changes were also reflected by the risk quotient (RQ) values calculated from the concentration and toxicity values. Pharmaceuticals such as telmisartan and carbamazepine and industrial chemicals such as organophosphorus flame retardants (OPFRs) and melamine accounted for approximately 90% of the total RQ. Major substances prioritized using the production of the RQ value and the detection frequency included OPFRs and telmisartan. It is recommended that these results be reflected in future water quality monitoring plans. (C) 2020 Elsevier Ltd. All rights reserved.

Formula: C13H10O. Welcome to talk about 119-61-9, If you have any questions, you can contact Park, N; Jeon, J or send Email.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

An article Copper-catalyzed sulfonylation of N-tosylhydrazones followed by a one-pot C-N bond formation WOS:000655654000001 published article about AMINES SYNTHESIS; HYDRAZONES; REAGENTS; DECOMPOSITION; DIHALOARENES; SULFONES; ROUTE in [Zhang, Kena; Provot, Olivier; Tran, Christine; Alami, Mouad; Hamze, Abdallah] Univ Paris Saclay, CNRS, BioCIS, Fac Pharm, F-92290 Chatenay Malabry, France in 2021.0, Cited 32.0. Formula: C13H10O. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

A new methodology to synthesize sulfonyl-N-phenylaniline derivatives via the trapping of bromo-sulfone derivatives generated from N-tosylhydrazones (NTHs) with amines is described. The reaction proved successful for a wide range of NTHs and amines and tolerated various functional groups on either coupling partner (35 examples). The mechanism was studied, and we showed that the sulfone formation does not follow a radical pathway.

Formula: C13H10O. Welcome to talk about 119-61-9, If you have any questions, you can contact Zhang, KN; Provot, O; Tran, C; Alami, M; Hamze, A or send Email.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

An article Mechanistically Guided Design of an Efficient and Enantioselective Aminocatalytic alpha-Chlorination of Aldehydes WOS:000651748000009 published article about RATIONALIZATION; CATALYSIS; PARADIGM in [Hutchinson, George; Alamillo-Ferrer, Carla; Bures, Jordi] Univ Manchester, Dept Chem, Manchester M13 9PL, Lancs, England in 2021.0, Cited 18.0. COA of Formula: C13H10O. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

The enantioselective aminocatalytic alpha-chlorination of aldehydes is a challenging reaction because of its tendency to proceed through neutral intermediates in unselective pathways. Herein we report the rational shift to a highly selective reaction pathway involving charged intermediates using hexafluoroisopropanol as solvent. This change in mechanism has enabled us to match and improve upon the yields and enantioselectivities displayed by previous methods while using cheaper aminocatalysts and chlorinating agents, 80-95% less amount of catalyst, convenient temperatures, and shorter reaction times.

Welcome to talk about 119-61-9, If you have any questions, you can contact Hutchinson, G; Alamillo-Ferrer, C; Bures, J or send Email.. COA of Formula: C13H10O

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

An article Preparation of CeO2-doped carbon nanotubes cathode and its mechanism for advanced treatment of pig farm wastewater WOS:000587290300139 published article about ELECTRO-FENTON PROCESS; GRAPHITE FELT; ELECTROCHEMICAL TREATMENT; PHOTOCATALYTIC ACTIVITY; DEGRADATION MECHANISM; OXYGEN; OXIDATION; REDUCTION; REMOVAL; PARAMETERS in [Kuang, Chaozhi; Xu, Yanbin; Xie, Guangyan; Pan, Zhanchang; Zheng, Li; Lai, Weikang; Ling, Jiayin; Talawar, Manjunatha; Zhou, Xiao] Guangdong Univ Technol, Sch Environm Sci & Engn, Guangzhou 51006, Peoples R China in 2021.0, Cited 45.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9. Application In Synthesis of Benzophenone

The effluent from conventional treatment process (including anaerobic digestion and anoxic-oxic treatment) for pig farm wastewater was difficult to treat due to its low ratio of biochemical oxygen demand to chemical oxygen demand (BOD5/CODCr) (<0.1). In the present study, electro-Fenton (EF) was used to improve the biodegradability of the mentioned effluent and the properties of self-prepared CeO2 doped multi-wall carbon nanotubes (MWCNTs) electrodes were also studied. An excellent H2O2 production (165 mg L-1) was recorded, after an 80-min electrolysis, when the mass ratio of MWCNTs, CeO2 and pore-forming agent (NH4HCO3) was 6:1:1. Results of scanning electron microscopy (SEM), transmission electron microscope (TEM) and x-ray photoelectron spectroscopy (XPS) showed that addition of NH4HCO3 and the doping of CeO2 could increase the superficial area of the electrode as well as the oxygen reduction reaction (ORR) electro-catalytic performance. The BOD5/CODCr of the wastewater from the first stage AO process increased from 0.08 to 0.45 and CODCr reduced 71.5% after an 80-min electrolysis, with 0.3 mM Fe2+ solution. The non-biodegradable chemical pollutants from the first stage AO process were degraded by EF. The non-biodegradable pollutants identified by LC-MS/MS in the effluent from AO process including aminopyrine, oxadixyl and 3-methyl-2-quinoxalinecarboxylic acid could be degraded by EF process, with the removal rates of 81.86%, 34.39% and 7.13% in 80 min, and oxytetracycline with the removal rate of 100% in 20 min. Therefore, electro-Fenton with the new CeO2-doped MWCNTs cathode electrode will be a promising supplement for advanced treatment of pig farm wastewater. (C) 2020 Elsevier Ltd. All rights reserved. Application In Synthesis of Benzophenone. Welcome to talk about 119-61-9, If you have any questions, you can contact Kuang, CZ; Xu, YB; Xie, GY; Pan, ZC; Zheng, L; Lai, WK; Ling, JY; Talawar, M; Zhou, X or send Email.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Gadde, K; Maes, BUW; Tehrani, KA in [Gadde, Karthik; Maes, Bert U. W.; Abbaspour Tehrani, Kourosch] Univ Antwerp, Dept Chem, Groenenborgerlaan 171, B-2020 Antwerp, Belgium published HFIP-mediated 2-aza-Cope rearrangement: metal-free synthesis of alpha-substituted homoallylamines at ambient temperature in 2021.0, Cited 80.0. Name: Benzophenone. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9.

An efficient metal-free strategy for the synthesis of alpha-substituted homoallylamine derivatives has been developed via a 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP)-promoted 2-aza-Cope rearrangement of aldimines, generated in situ by condensation of aldehydes with easily accessible 1,1-diphenylhomoallylamines. This reaction provides rapid access to alpha-substituted homoallylamines with excellent functional group tolerance and yields. The reaction takes place at room temperature and no chromatographic purification is required for product isolation. The synthetic utility of the current method is further demonstrated by the transformation of the obtained benzophenone ketimines into N-unprotected homoallylamines, an alpha-amino alcohol and an alpha-amino amide.

Name: Benzophenone. Bye, fridends, I hope you can learn more about C13H10O, If you have any questions, you can browse other blog as well. See you lster.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Application In Synthesis of Benzophenone. Authors Young, TM; Black, GP; Wong, L; Bloszies, CS; Fiehn, O; He, GC; Denison, MS; Vogel, CFA; Durbin-Johnson, B in AMER CHEMICAL SOC published article about in [Young, Thomas M.; Black, Gabrielle P.; Wong, Luann] Univ Calif Davis, Dept Civil & Environm Engn, Davis, CA 95616 USA; [Young, Thomas M.; Black, Gabrielle P.; Bloszies, Clayton S.; Fiehn, Oliver] Univ Calif Davis, Agr & Environm Chem Grad Grp, Davis, CA 95616 USA; [Bloszies, Clayton S.; Fiehn, Oliver] Univ Calif Davis, West Coast Metabol Ctr, Davis, CA 95616 USA; [He, Guochun; Denison, Michael S.; Vogel, Christoph F. A.] Univ Calif Davis, Dept Environm Toxicol, Davis, CA 95616 USA; [Vogel, Christoph F. A.] Univ Calif Davis, Ctr Hlth & Environm, Davis, CA 95616 USA; [Durbin-Johnson, Blythe] Univ Calif Davis, Sch Med, Div Biostat, Davis, CA 95616 USA in 2021.0, Cited 45.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

Urban wildfires may generate numerous unidentified chemicals of toxicity concern. Ash samples were collected from burned residences and from an undeveloped upwind reference site, following the Tubbs fire in Sonoma County, California. The solvent extracts of ash samples were analyzed using GC- and LC-high-resolution mass spectrometry (HRMS) and using a suite of in vitro bioassays for their bioactivity toward nuclear receptors [aryl hydrocarbon receptor (AhR), estrogen receptor (ER), and androgen receptor (AR)], their influence on the expression of genetic markers of stress and inflammation [interleukin-8 (IL-8) and cyclooxygenase-2 (COX-2)], and xenobiotic metabolism [cytochrome P4501A1 (CYP1A1)]. Genetic markers (CYP1A1, IL-8, and COX-2) and AhR activity were significantly higher with wildfire samples than in solvent controls, whereas AR and ER activities generally were unaffected or reduced. The bioassay responses of samples from residential areas were not significantly different from the samples from the reference site despite differing chemical compositions. Suspect and nontarget screening was conducted to identify the chemicals responsible for elevated bioactivity using the multiple streams of HRMS data and open-source data analysis workflows. For the bioassay endpoint with the largest available database of pure compound results (AhR), nontarget features statistically related to whole sample bioassay response using Spearman’s rank-order correlation coefficients or elastic net regression were significantly more likely (by 10 and 15 times, respectively) to be known AhR agonists than the overall population of compounds tentatively identified by nontarget analysis. The findings suggest that a combination of nontarget analysis, in vitro bioassays, and statistical analysis can identify bioactive compounds in complex mixtures.

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Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem