Category: 150-19-6

Name: m-Methoxyphenol. Authors Bellotti, P; Koy, M; Gutheil, C; Heuvel, S; Glorius, F in ROYAL SOC CHEMISTRY published article about in [Bellotti, Peter; Koy, Maximilian; Gutheil, Christian; Heuvel, Steffen; Glorius, Frank] Westfal Wilhelms Univ Munster, Organ Chem Inst, Corrensstr 40, D-48149 Munster, Germany in 2021, Cited 66. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6

A highly modular radical cascade strategy based upon radical cyclisation/allylic substitution sequence between alkyl/aryl bromides, 1,3-dienes and nucleophiles ranging from sulfinates to amines, phenols and 1,3-dicarbonyls is described (>80 examples). Palladium phosphine complexes – which merge properties of photo- and cross coupling-catalysts – allow to forge three bonds with complete 1,4-selectivity and stereocontrol, delivering highly value added carbocyclic and heterocyclic motifs that can feature – inter alia – vicinal quaternary centers, free protic groups, gem-difluoro motifs and strained rings. Furthermore, a flow chemistry approach was for the first time applied in palladium-photocatalysed endeavors involving radicals.

Name: m-Methoxyphenol. About m-Methoxyphenol, If you have any questions, you can contact Bellotti, P; Koy, M; Gutheil, C; Heuvel, S; Glorius, F or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Application In Synthesis of m-Methoxyphenol. Authors Song, CY; Nie, JQ; Ma, C; Lu, CF; Wang, FY; Yang, GC in ELSEVIER published article about in [Song, Chaoyang; Nie, Junqi; Ma, Chao; Lu, Cuifen; Wang, Feiyi; Yang, Guichun] Hubei Univ, Coll Chem & Chem Engn, Hubei Collaborat Innovat Ctr Adv Organ Chem Mat, Minist Educ Key Lab Synth & Applicat Organ Funct, Wuhan 430062, Peoples R China in 2021, Cited 71. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6

1,2,3-Triazole contained conjugated porous polymers (CPPs) have recently emerged as a new class of efficient photocatalysts. To gain more insight into the excellent photocatalytic activity of this kind of CPPs, herein, we report the design and preparation of a series of 1,2,3-triazole-based CPPs via oxidative coupling polymerization to study their photocatalytic performance. These CPPs have donor-acceptor properties and 1,2,3-triazole serves as an electron acceptor. The resulting CPPs with thiophene, carbazole and diphenylamine as electron donor units, respectively, have distinct porosities and optoelectronic properties, and showed effective photocatalytic performance towards oxidative hydroxylation of arylboric acids and alkylation of vinylarenes with diethyl bromomalonate or bromoacetonitrile. The thiophene contained CPP was a more efficient photocatalyst for the catalytic reactions, which can be attributed to its smaller optical band gap and greater charge separation effi-ciency. Furthermore, PTPT has shown reliable recyclability with no significant loss in its catalytic activity.

About m-Methoxyphenol, If you have any questions, you can contact Song, CY; Nie, JQ; Ma, C; Lu, CF; Wang, FY; Yang, GC or concate me.. Application In Synthesis of m-Methoxyphenol

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

COA of Formula: C7H8O2. Recently I am researching about HOMOPROPARGYLIC ALCOHOLS; ENOL-ETHERS; CYCLOISOMERIZATION; HYDROAMINATION; BOND; HYDROALKOXYLATION; CYCLIZATION; INDOLES; ACETALS; ROUTE, Saw an article supported by the National Institutes of Health (NIGMS)United States Department of Health & Human ServicesNational Institutes of Health (NIH) – USANIH National Institute of General Medical Sciences (NIGMS) [R01GM110560]; NIHUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) – USA [S10RR028859]; NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCESUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) – USANIH National Institute of General Medical Sciences (NIGMS) [R01GM110560] Funding Source: NIH RePORTER. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Costello, JP; Ferreira, EM. The CAS is 150-19-6. Through research, I have a further understanding and discovery of m-Methoxyphenol

The steric and electronic drivers of regioselectivity in platinum -catalyzed intramolecular hydroalkoxylation are elucidated. A branch point is found that divides the process between 5-exo and 6-endo selective processes, and enol ethers can be accessed in good yields for both oxygen heterocycles. The main influence arises from an electronic effect, where the alkyne substituent induces a polarization of the alkyne that leads to preferential heteroatom attack at the more electron -deficient carbon. The electronic effects are studied in other contexts, including hydroacyloxylation and hydroamination, and similar trends in directionality are predominant although not uniformly observed.

COA of Formula: C7H8O2. About m-Methoxyphenol, If you have any questions, you can contact Costello, JP; Ferreira, EM or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Recently I am researching about SUPERCRITICAL WATER GASIFICATION; PRESSURE AQUEOUS ENVIRONMENTS; HOT COMPRESSED WATER; HYDROGEN-PRODUCTION; BIOMASS GASIFICATION; CHEMICAL-REACTIONS; CELLULOSE; LIGNIN; CONVERSION; PYROLYSIS, Saw an article supported by the Scientific and Technological Research Council of Turkey (TUBITAK)Turkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [109M284]. Product Details of 150-19-6. Published in ELSEVIER in AMSTERDAM ,Authors: Gokkaya, DS; Cokkuvvetli, T; Saglam, M; Yuksel, M; Ballice, L. The CAS is 150-19-6. Through research, I have a further understanding and discovery of m-Methoxyphenol

In this study, poplar wood chips were gasified in sub-and supercritical water as biomass feedstock. Hydrothermal gasification experiments were performed to examine how the reaction temperature and different type of catalysts influence conversion efficiency. The effectiveness of commercially available [alkali catalyst; KOH], naturally available [mineral catalysts; Trona [Na-3(CO3)(HCO3)center dot 2H(2)O], Dolomite [CaMg(CO3)(2)] and Borax [Na2B4O7 center dot 10H(2)O] and laboratory-prepared catalysts [metal-impregnated activated carbons; (Ni/AC) and (Ru/AC)] have been demonstrated so as to shift the product distribution toward more desirable compounds. Gaseous compound yield was increased from 29.7% to 79.3% with respect to increasing temperature while liquid compound yield decreased from 27.6% to 1.1% and solid residue from 38.0% to 15.6%. The highest H-2 (20.1 mol/kg C in poplar) and CH4 (12.7 mol/kg C in poplar) yields were obtained with Ru/AC catalyst. Carboxylic acids and 5-methyl furfural were determined as the main liquid compounds. (C) 2019 Elsevier B.V. All rights reserved.

Product Details of 150-19-6. About m-Methoxyphenol, If you have any questions, you can contact Gokkaya, DS; Cokkuvvetli, T; Saglam, M; Yuksel, M; Ballice, L or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Recently I am researching about CORRELATED MOLECULAR CALCULATIONS; C-H FUNCTIONALIZATION; GAUSSIAN-BASIS SETS; CHAIN PROCESSES; CONVERSION; OXIDATION; REDUCTION; PHENOLS; ELECTROSYNTHESIS; APPROXIMATIONS, Saw an article supported by the German Research Foundation (DFG)German Research Foundation (DFG) [FR 3848/3-1]; DFG through Emmy-Noether projectGerman Research Foundation (DFG) [RO 5688/1-1]; RoHan Project – German Academic Exchange Service (DAAD)Deutscher Akademischer Austausch Dienst (DAAD) [57315854]; Federal Ministry for Economic Cooperation and Development (BMZ). Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Roesel, AF; Ugandi, M; Huyen, NTT; Majek, M; Broese, T; Roemelt, M; Francke, R. The CAS is 150-19-6. Through research, I have a further understanding and discovery of m-Methoxyphenol. Computed Properties of C7H8O2

The facilitation of redox-neutral reactions by electrochemical injection of holes and electrons, also known as electrochemical catalysis, is a little explored approach that has the potential to expand the scope of electrosynthesis immensely. To systematically improve existing protocols and to pave the way toward new developments, a better understanding of the underlying principles is crucial. In this context, we have studied the Newman-Kwart rearrangement of O-arylthiocarbamates to the corresponding S-aryl derivatives, the key step in the synthesis of thiophenols from the corresponding phenols. This transformation is a particularly useful example because the conventional method requires temperatures up to 300 degrees C, whereas electrochemical catalysis facilitates the reaction at room temperature. A combined experimental-quantum chemical approach revealed several reaction channels and rendered an explanation for the relationship between the structure and reactivity. Furthermore, it is shown how rapid cyclic voltammetry measurements can serve as a tool to predict the feasibility for specific substrates. The study also revealed distinct parallels to photoredox-catalyzed reactions, in which back-electron transfer and chain propagation are competing pathways.

About m-Methoxyphenol, If you have any questions, you can contact Roesel, AF; Ugandi, M; Huyen, NTT; Majek, M; Broese, T; Roemelt, M; Francke, R or concate me.. Computed Properties of C7H8O2

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Formula: C7H8O2. Sarma, D; Majumdar, B; Sarma, TK in [Sarma, Daisy; Majumdar, Biju; Sarma, Tridib K.] Indian Inst Technol Indore, Sch Basic Sci, Discipline Chem, Khandwa Rd, Indore 453552, India published Visible-light induced enhancement in the multi-catalytic activity of sulfated carbon dots for aerobic carbon-carbon bond formation in 2019, Cited 39. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6.

The development of carbonaceous materials as metal-free catalysts integrating different types of catalysis in a single system represents a significant advance in cascade/tandem organic synthesis. Zero-dimensional carbon dots with tuneable optical properties and easily modifiable surface functionalities can be harnessed as a carbocatalyst for merging photooxidation and acid-catalyzed reactions in one pot. Herein, we explore carbon dots decorated with hydrogen sulfate groups as a photocatalyst for the dehydrogenative cross-coupling of xanthenes with ketones, arenes and 1,3-dicarbonyl compounds that showed high efficiency and selectivity under visible-light irradiation. The sulphated carbon dots demonstrate dual catalytic properties, wherein they induced the rapid photooxidation of xanthenes in the presence of molecular oxygen to form a hydroperoxy intermediate followed by coupling of nucleophiles catalysed by the acidic surface functional groups. The methodology represents an operationally simple pathway for the generation of C-C coupling products in a short reaction time with wide substrate scopes under mild conditions. The catalyst is easily separable and can be reused over multiple cycles with good efficiency.

Formula: C7H8O2. About m-Methoxyphenol, If you have any questions, you can contact Sarma, D; Majumdar, B; Sarma, TK or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Product Details of 150-19-6. Bugaenko, DI; Yurovskaya, MA; Karchava, AV in [Bugaenko, Dmitry, I; Yurovskaya, Marina A.; Karchava, Alexander, V] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119992, Russia published Reaction of Pyridine-N-Oxides with Tertiary sp(2)-N-Nucleophiles: An Efficient Synthesis of Precursors for N-(Pyrid-2-yl)-Substituted N-Heterocyclic Carbenes in 2020, Cited 61. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6.

N-(Pyrid-2-yl)-substituted azolium and pyridinium salts, precursors for hybrid NHC-containing ligands, were obtained with excellent regioselectivity, employing a deoxygenative CH-functionalization of pyridine-N-oxides with substituted imidazoles, thiazoles, and pyridine. Unlike the traditional SNAr-based methods, this approach provides high yields for substrates bearing substituents of different electronic nature. The utility of azolium and pyridinium salts thus prepared was also highlighted by the synthesis of pyridyl-substituted imidazolyl-2-thione, benzodiazepine as well as 2-aminopyridines.

Product Details of 150-19-6. About m-Methoxyphenol, If you have any questions, you can contact Bugaenko, DI; Yurovskaya, MA; Karchava, AV or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Quality Control of m-Methoxyphenol. Gendron, T; Pereira, R; Abdi, HY; Witney, TH; Arstad, E in [Gendron, Thibault; Arstad, Erik] UCL, Ctr Radiopharmaceut Chem, 5 Gower Pl, London WC1E 6BS, England; [Gendron, Thibault; Abdi, Hafsa Y.; Arstad, Erik] UCL, Dept Chem, 20 Gordon St, London WC1H 0AJ, England; [Pereira, Raul; Witney, Timothy H.] UCL, Ctr Adv Biomed Imaging, 72 Huntley St, London WC1E 6DD, England; [Pereira, Raul; Witney, Timothy H.] Kings Coll London, St Thomas Hosp, Sch Biomed Engn & Imaging Sci, Dept Imaging Chem & Biol, London SE1 7EH, England published Iron(II)/Persulfate Mediated Newman-Kwart Rearrangement in 2020.0, Cited 20.0. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6.

Herein, we report that iron(II)/ammonium persulfate in aqueous acetonitrile mediates the Newman-Kwart rearrangement of O-aryl carbamothioates. Electron-rich substrates react rapidly under moderate heating to afford the rearranged products in excellent yields. The mild conditions, rapid reaction rates, and suitability for scale up offers immediate practical benefits to access functionalized thiophenols.

Quality Control of m-Methoxyphenol. About m-Methoxyphenol, If you have any questions, you can contact Gendron, T; Pereira, R; Abdi, HY; Witney, TH; Arstad, E or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Recently I am researching about ONE-POT SYNTHESIS; MARINE SPONGE; BIOLOGICAL-ACTIVITY; EFFICIENT SYNTHESIS; TERMINAL ALKYNES; O-ALKYNYLPHENOLS; FACILE SYNTHESIS; ALKENYL PHENOLS; C-C; MICROWAVE, Saw an article supported by the Department of Science and Technology-Science and Engineering Research Board (DST-SERB), New Delhi [EMR/2017/005312]; UGCUniversity Grants Commission, India; DST-SERBDepartment of Science & Technology (India)Science Engineering Research Board (SERB), India. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Aggarwal, S; Srinivas, D; Sreenivasulu, C; Satyanarayana, G. The CAS is 150-19-6. Through research, I have a further understanding and discovery of m-Methoxyphenol. COA of Formula: C7H8O2

Recent research has been focused on the transition metal-catalyzed reactions. Herein we have developed nickel-catalyzed synthesis of 3-aryl benzofurans fromortho-alkenyl phenolsviaintramolecular dehydrogenative coupling. Notably, simple O(2)gas served as an oxidant, without using any sacrificial hydrogen acceptor. The strategy enabled the synthesis of 3-aryl benzofurans in good to excellent yields.

About m-Methoxyphenol, If you have any questions, you can contact Aggarwal, S; Srinivas, D; Sreenivasulu, C; Satyanarayana, G or concate me.. COA of Formula: C7H8O2

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Product Details of 150-19-6. Authors Fereidoonnezhad, M; Tabaei, SMH; Sakhteman, A; Seradj, H; Faghih, Z; Faghih, Z; Mojaddami, A; Sadeghian, B; Rezaei, Z in ELSEVIER published article about in [Fereidoonnezhad, Masood; Mojaddami, Ayyub] Ahvaz Jundishapur Univ Med Sci, Sch Pharm, Dept Med Chem, Ahvaz, Iran; [Fereidoonnezhad, Masood; Tabaei, S. Mohammad Hossein; Sakhteman, Amirhossein; Seradj, Hassan; Faghih, Zeinab; Mojaddami, Ayyub; Sadeghian, Batool; Rezaei, Zahra] Shiraz Univ Med Sci, Dept Med Chem, Sch Pharm, Shiraz, Iran; [Fereidoonnezhad, Masood; Tabaei, S. Mohammad Hossein; Sakhteman, Amirhossein; Seradj, Hassan; Faghih, Zeinab; Mojaddami, Ayyub; Sadeghian, Batool; Rezaei, Zahra] Shiraz Univ Med Sci, Pharmaceut Sci Res Ctr, Sch Pharm, Shiraz, Iran; [Faghih, Zahra] Shiraz Univ Med Sci, Sch Med, Shiraz Inst Canc Res, Shiraz, Iran in 2020, Cited 38. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6

Dichloroacetate (DCA) as a mitochondria-targeting small molecule, through inhibition of pyruvate dehydrogenase kinases (PDK1-4), promotes mitochondria-regulated apoptosis and hence, inhibits tumour growth and reduces its proliferation. In this study, a series of novel N-aryl-2,2-dichloroacetamide and aryl-2,2-dichloroacetate derivatives were designed and synthesized. Their cytotoxic activities against various human cancer cell lines including A549, HCA-7, MCF-7, MDA-MB-231, KB and SKOV3 were evaluated. These compounds showed satisfactory potencies with much higher anticancer activity than the parent compound DCA, against the studied cancer cell lines. Molecular docking studies were also done to find their binding site and types of their interactions with PDKs isoenzymes. Among the synthesized compounds, 2,2-dichloro-N-(9,10-dioxo-9,10-dihydroanthracen-1-yl)acetamide (f1) can also induce A549 cells apoptosis. Therefore, compound f1 might have a potential value for further study in drug development. QSAR studies of this class of compounds were also explored using a collection of chemometrics methods. (C) 2020 Published by Elsevier B.V.

Product Details of 150-19-6. About m-Methoxyphenol, If you have any questions, you can contact Fereidoonnezhad, M; Tabaei, SMH; Sakhteman, A; Seradj, H; Faghih, Z; Faghih, Z; Mojaddami, A; Sadeghian, B; Rezaei, Z or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles