What unique challenges do researchers face in 6H-Benzo[c]chromen-6-one

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Recommanded Product: 6H-Benzo[c]chromen-6-one. Authors Rumyantsev, AV; Pichugov, AV; Bushkov, NS; Aleshin, DY; Strelkova, TV; Lependina, OL; Zhizhko, PA; Zarubin, DN in ROYAL SOC CHEMISTRY published article about in [Rumyantsev, Andrey, V; Pichugov, Andrey, V; Bushkov, Nikolai S.; Aleshin, Dmitry Yu; Strelkova, Tatyana, V; Lependina, Olga L.; Zhizhko, Pavel A.; Zarubin, Dmitry N.] Russian Acad Sci, AN Nesmeyanov Inst Organoelement Cpds, Vavilov Str 28, Moscow 119991, Russia; [Rumyantsev, Andrey, V; Bushkov, Nikolai S.] Moscow MV Lomonosov State Univ, Dept Chem, Vorobevy Gory 1, Moscow 119991, Russia; [Pichugov, Andrey, V; Aleshin, Dmitry Yu] D Mendeleev Univ Chem Technol Russia, Higher Chem Coll, Miusskaya Sq 9, Moscow 125047, Russia in 2021.0, Cited 33.0. The Name is 6H-Benzo[c]chromen-6-one. Through research, I have a further understanding and discovery of 2005-10-9

We report the first examples of direct imidation of lactones giving the corresponding cyclic imidates via oxo/imido heterometathesis with N-sulfinylamines catalysed by a well-defined silica-supported Ti imido complex.

Recommanded Product: 6H-Benzo[c]chromen-6-one. Welcome to talk about 2005-10-9, If you have any questions, you can contact Rumyantsev, AV; Pichugov, AV; Bushkov, NS; Aleshin, DY; Strelkova, TV; Lependina, OL; Zhizhko, PA; Zarubin, DN or send Email.

Reference:
Article; Zhang, Jian; Shi, Dongdong; Zhang, Haifeng; Xu, Zheng; Bao, Hanyang; Jin, Hongwei; Liu, Yunkui; Tetrahedron; vol. 73; 2; (2017); p. 154 – 163;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Why do aromatic interactions matter of compound:6H-Benzo[c]chromen-6-one

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Recommanded Product: 2005-10-9. Recently I am researching about C-H AMINATION; EXCITED-STATE; LIGNIN; BENZENE; SPIROCYCLIZATION; NAPHTHALENE; DERIVATIVES; CYCLIZATION; OXIDATION; CLEAVAGE, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21711530020, 21721004, 21690082, 21690084, 21690080]; Strategic Priority Research Program of the Chinese Academy of SciencesChinese Academy of Sciences [XDB17020300, XDB17000000]; STINT [CH2016-6755]; NSFCNational Natural Science Foundation of China (NSFC); Swedish Energy AgencySwedish Energy Agency [P39427-1]. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Li, HJ; Subbotina, E; Bunrit, A; Wang, F; Samec, JSM. The CAS is 2005-10-9. Through research, I have a further understanding and discovery of 6H-Benzo[c]chromen-6-one

The idea of using biaryl structures to generate synthetic building blocks such as spirolactones is attractive because biaryl structures are abundant in biomass waste streams. However, the inertness of aromatic rings of biaryls makes it challenging to transform them into functionalized structures. In this work, we developed photoinduced dearomatization of nonphenolic biaryl compounds to generate spirolactones. We demonstrate that dearomatization can be performed via either aerobic photocatalysis or anaerobic photooxidation to tolerate specific synthetic conditions. In both pathways, dearomatization is induced by electrophilic attack of the carboxyl radical. The resulting spirodiene radical is captured by either oxygen or water in aerobic and anaerobic systems, respectively, to generate the spirodienone. These methods represent novel routes to synthesize spirolactones from the biaryl motif.

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Reference:
Article; Zhang, Jian; Shi, Dongdong; Zhang, Haifeng; Xu, Zheng; Bao, Hanyang; Jin, Hongwei; Liu, Yunkui; Tetrahedron; vol. 73; 2; (2017); p. 154 – 163;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Our Top Choice Compound: 1159408-65-7

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Today I’d like to introduce a new chemical compound, CAS is 1159408-65-7, Name is 4,8-Dioxa-12,16-diazaheneicosanamide, 6-amino-11,17-dioxo-6-[[3-oxo-3-[[3-[[1-oxo-5-[[3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxy-β-D-galactopyranosyl]oxy]pentyl]amino]propyl]amino]propoxy]methyl]-N-[3-[[1-oxo-5-[[3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxy-β-D-galactopyranosyl]oxy]pentyl]amino]propyl]-21-[[3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxy-β-D-galactopyranosyl]oxy]-, 2,2,2-trifluoroacetate, Formula is C81H129F3N10O38, Molecular Weight is 1907.93g/mol. Because of its complex structure and huge molecular weight, this compound is rarely understood. Now let me introduce some knowledge about its synthesis.. Safety of 1159408-65-7

The general reactant of this compound is 5-[[3,4,6-Tri-O-acetyl-2-(acetylamino)-2-deoxy-β-D-galactopyranosyl]oxy]pentanoic acid;Phenylmethyl N-[2-[3-[(3-aminopropyl)amino]-3-oxopropoxy]-1,1-bis[[3-[(3-aminopropyl)amino]-3-oxopropoxy]methyl]ethyl]carbamate, Reagents is 1-Hydroxybenzotriazole,Diisopropylethylamine,1-[Bis(dimethylamino)methylene]-1H-benzotriazolium hexafluorophosphate(1-) 3-oxide, Catalyst(), Solvent is Dimethylformamide, Products Phenylmethyl 8,14-dioxo-3,3-bis[[3-oxo-3-[[3-[[1-oxo-5-[[3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxy-β-D-galactopyranosyl]oxy]pentyl]amino]propyl]amino]propoxy]methyl]-18-[[3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxy-β-D-galactopyranosyl]oxy]-5-oxa-2,9,13-triazaoctadecanoate, Yield: 58%, Synthetic Methods procedure :1. Add HOBt ( 25.00 g, 0.16 mmol ) and HBTU ( 75.15 g, 198.15 mmol ) to a solution of triamine ( 35.0 g, 54 mmol ) and the acid ( 80.54 g, 180.10 mmol ) in DMF ( 300 mL ) ., 2. Add DIEA ( 94 mL, 544 mmol ) slowly to above mixture., 3. Stir the reaction for 3 hours at room temperature, dilute with water and extract the mixture with ether ( 300 mL ) ., 4. Separate the water phase, extract with DCM ( 2 x 500 mL ) and wash the combined organic layers consecutively with saturated NaHCO3 ( 400 mL ) , water ( 2 x 300 mL ) and brine ( 300 mL ) ., 5. Dry over anhydrous Na2SO4, evaporate the solvent under reduced pressure., Transfornation (Acylation of Nitrogen Nucleophiles by Carboxylic Acids. Characterization Data include ‘s Proton NMR Spectrum : ( 400 MHz, DMSO-d 6 ) : δ 7.87–7.76 ( m, 6H, NH ) ; 7.71 ( t, J = 5.7 Hz, 3H, NH ) ; 7.37-7.25 ( m, 5H ) ; 6.52 ( brs, 1H, NH ) ; 5.20 ( d, J = 3.4 Hz, 3H, sugar H4 ) ; 5.00–4.92 ( m, 5H ) ; 4.47 ( d, J = 8.5 Hz, 3H, sugar H1 ) ; 4.06–3.97 ( m, 9H, sugar H5, H6, H6′ ) ; 3.86 ( dt, J = 8.8, 11.1 Hz, 3H, sugar H2 ) ; 3.69 ( dt, J = 5.6, 9.9 Hz, 3H ) ; 3.53 ( t, J = 6.4 Hz, 6H ) ; 3.47 ( s broad, 6H ) ; 3.39 ( dt, J = 6.4, 9.9 Hz, 3H ) ; 3.07-2.97 ( m, 12H ) ; 2.26 ( t, J = 6.4 Hz, 6H ) ; 2.09 ( s, 9H ) ; 2.03 ( t, J = 7.0 Hz, 6H ) ; 1.98 ( s, 9H ) ; 1.88 ( s, 9H ) ; 1.76 ( s, 9H ) ; 1.58–1.35 ( m, 18H ) ., Carbon-13 NMR : ( 126 MHz, DMSO-d 6 ) : δ171.9, 170.0, 169.9, 169.9, 169.6, 169.4, 137.2, 128.3, 127.7, 127.5, 101.0, 79.2, 70.5, 69.8, 68.7, 68.2, 67.3, 66.7, 61.4, 58.8, 49.4, 36.4, 36.3, 36.1, 35.0, 29.3, 28.6, 22.8, 21.8, 20.5, 20.5, 20.4., HRMS: Mass calc. for C87H134N10O38: 1926.88; found: 1949.89 [M+Na+, MALDI-TOF, matrix: 2- ( 4-hydroxyphenylazo ) benzoic acid ( HABA ) ]., State is pale yellow solid

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Reference:
CAS Method Number 3-353-CAS-9716164,
,CAS Method Number 3-367-CAS-11845945

Machine Learning in Chemistry about C13H8O2

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In 2019.0 CHEMISTRYSELECT published article about BAEYER-VILLIGER OXIDATION; SELECTIVE OXIDATION; AROMATIC-ALDEHYDES; CATALYTIC THIOCYANATION; EFFICIENT BROMINATION; SODIUM PERCARBONATE; BENZYLIC ALCOHOLS; HYDROGEN-PEROXIDE; AMIDATION; EPOXIDATION in [Khosravi, Kaveh; Naserifar, Shirin] Arak Univ, Dept Chem, Fac Sci, Arak 3815688349, Iran in 2019.0, Cited 61.0. The Name is 6H-Benzo[c]chromen-6-one. Through research, I have a further understanding and discovery of 2005-10-9. HPLC of Formula: C13H8O2

Urea-2,2-dihydroperoxypropane (UDHPP)- a white crystalline solid oxidant which is formed when urea is recrystallized from dihydroperoxypropane- was applied as the terminal oxidant in several oxidative procedures namely epoxidation of alpha, beta-unsaturated ketones and alkenes, oxidation of sulfides to sulfoxides and sulfones, bayer-villeger reaction, bromination and iodation of aniline and phenol derivatives, oxidative esterification, oxidative amidation of aromatic aldehydes, thiocyanation of aromatic compounds, and oxidation of pyridines, oxidation of secondary, allylic and benzylic alcohols. All the approaches were carried out under mild conditions and short reaction times and afforded the corresponding products in high yields.

HPLC of Formula: C13H8O2. Bye, fridends, I hope you can learn more about C13H8O2, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Article; Zhang, Jian; Shi, Dongdong; Zhang, Haifeng; Xu, Zheng; Bao, Hanyang; Jin, Hongwei; Liu, Yunkui; Tetrahedron; vol. 73; 2; (2017); p. 154 – 163;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

More research is needed about 103-25-3

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I found the field of Chemistry very interesting. Saw the article C-C Bond Cleavage of Unactivated 2-Acylimidazoles published in 2020.0. Recommanded Product: 103-25-3, Reprint Addresses Morimoto, H; Ohshima, T (corresponding author), Kyushu Univ, Grad Sch Pharmaceut Sci, Fukuoka 8128582, Japan.. The CAS is 103-25-3. Through research, I have a further understanding and discovery of Methyl 3-phenylpropionate

2-Acylimidazoles are widely used as post-transformable carboxylic acid equivalents in chemoselective and enantioselective reactions. Their transformations, however, require pretreatment with highly reactive, toxic methylating reagents to facilitate C-C bond cleavage. Here, we demonstrate that such pretreatment can be avoided and the C-C bond cleaved under neutral conditions without the use of additional reagents or catalysts. The scope of the reaction, including the use of products reported in the literature as substrates, and some mechanistic insights are described.

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Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

The important role of C10H10O2

HPLC of Formula: C10H10O2. Bye, fridends, I hope you can learn more about C10H10O2, If you have any questions, you can browse other blog as well. See you lster.

HPLC of Formula: C10H10O2. Kielmann, M; Flanagan, KJ; Senge, MO in [Kielmann, Marc; Flanagan, Keith J.; Senge, Mathias O.] Univ Dublin, Trinity Coll Dublin, Sch Chem, Trinity Biomed Sci Inst,SFI Tetrapyrrole Lab, Dublin 2, Ireland published Targeted Synthesis of Regioisomerically Pure Dodecasubstituted Type I Porphyrins through the Exploitation of Peri-interactions in 2020.0, Cited 45.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4.

A targeted synthesis of dodecasubstituted type I porphyrins that utilizes the reaction of unsymmetrical 3,4-difunctionalized pyrroles and sterically demanding aldehydes was developed. This way, type I porphyrins could be obtained as the only type isomers, likely due to a minimization of the steric strain arising from peri-interactions. Uniquely, this method does not depend on lengthy precursor syntheses, the separation of isomers, or impractical limitations of the scale. In addition, single-crystal X-ray analysis was used to elucidate the structural features of the macrocycles.

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Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Top Picks: new discover of 2005-10-9

Bye, fridends, I hope you can learn more about C13H8O2, If you have any questions, you can browse other blog as well. See you lster.. Application In Synthesis of 6H-Benzo[c]chromen-6-one

Application In Synthesis of 6H-Benzo[c]chromen-6-one. I found the field of Chemistry very interesting. Saw the article Mesityl or Imide Acridinium Photocatalysts: Accessible Versus Inaccessible Charge-Transfer States in Photoredox Catalysis published in 2019.0, Reprint Addresses Aleman, J (corresponding author), Univ Autonoma Madrid, Fac Ciencias, Organ Chem Dept, Modulo 1,Calle Francisco Tomcis y Valiente 7, E-28049 Madrid, Spain.; Mancheno, OG (corresponding author), Univ Munster, Organ Chem Inst, Corrensstr 40, D-48149 Munster, Germany.; Aleman, J (corresponding author), Univ Autonoma Madrid, Fac Ciencias, Inst Adv Res Chem Sci IAdChem, Calle Francisco Tomcis y Valiente 7, E-28049 Madrid, Spain.. The CAS is 2005-10-9. Through research, I have a further understanding and discovery of 6H-Benzo[c]chromen-6-one.

A study on C9-imide acridinium photocatalysts with enhanced photoredox catalytic activity with respect to the well-established C9-mesityl acridinium salt is presented. The differences observed rely on the diverse accessibility of singlet charge-transfer excited states, which have been proven by CASPT2/CASSCF calculations, fluorescence and quenching studies.

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Reference:
Article; Zhang, Jian; Shi, Dongdong; Zhang, Haifeng; Xu, Zheng; Bao, Hanyang; Jin, Hongwei; Liu, Yunkui; Tetrahedron; vol. 73; 2; (2017); p. 154 – 163;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Downstream Synthetic Route Of Methyl 3-phenyl-2-propenoate

SDS of cas: 103-26-4. Welcome to talk about 103-26-4, If you have any questions, you can contact Micheli, L; Mannelli, LD; Mattoli, L; Tamimi, S; Flamini, E; Garetto, S; Lucci, J; Giovagnoni, E; Cinci, L; D’Ambrosio, M; Luceri, C; Ghelardini, C or send Email.

Micheli, L; Mannelli, LD; Mattoli, L; Tamimi, S; Flamini, E; Garetto, S; Lucci, J; Giovagnoni, E; Cinci, L; D’Ambrosio, M; Luceri, C; Ghelardini, C in [Micheli, Laura; Di Cesare Mannelli, Lorenzo; Cinci, Lorenzo; D’Ambrosio, Mario; Luceri, Cristina; Ghelardini, Carla] Univ Florence, Dept Neurosci Psychol Drug Res & Child Hlth NEURO, Pharmacol & Toxicol Sect, Viale Gaetano Pieraccini 6, I-50139 Florence, Italy; [Mattoli, Luisa; Tamimi, Sara; Flamini, Enrico; Garetto, Stefano; Lucci, Jacopo; Giovagnoni, Emiliano] Aboca SpA Soc Agr, Innovat & Med Sci Div, Loc Aboca 20, I-52037 Sansepolcro, Italy; [Garetto, Stefano; Lucci, Jacopo] Nat Biomed SpA, Loc Aboca 20, I-52037 Sansepolcro, Italy published Intra-Articular Route for the System of Molecules 14G1862 fromCentella asiatica: Pain Relieving and Protective Effects in a Rat Model of Osteoarthritis in 2020.0, Cited 74.0. SDS of cas: 103-26-4. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4.

Current pharmacological therapies for the management of chronic articular diseases are far from being satisfactory, so new strategies need to be investigated. We tested the intra-articular pain relieving properties of a system of molecules from a characterizedCentella asiaticaextract (14G1862) in a rat model of osteoarthritis induced by monoiodoacetate (MIA). 14G1862 (0.2-2 mg mL(-1)) was intra-articularly (i.a.) injected 7 days after MIA, behavioural and histological evaluations were performed 14, 30 and 60 days after treatments. Moreover, the effect of 14G1862 on nitrate production and iNOS expression in RAW 264.7 macrophages stimulated with LPS was assessed. In vitro, 14G1862 treatment attenuated LPS-induced NO production and iNOS expression in a comparable manner to celecoxib. In vivo, 14G1862 significantly reduced mechanical allodynia and hyperalgesia, spontaneous pain and motor alterations starting on day 14 up to day 60. The efficacy was higher or comparable to that evoked by triamcinolone acetonide (100 mu g i.a.) used as reference drug. Histological evaluation highlighted the improvement of several morphological parameters in MIA + 14G1862-treated animals with particularly benefic effects on joint space and fibrin deposition. In conclusion, i.a. treatment withCentella asiaticais a candidate to be a novel effective approach for osteoarthritis therapy.

SDS of cas: 103-26-4. Welcome to talk about 103-26-4, If you have any questions, you can contact Micheli, L; Mannelli, LD; Mattoli, L; Tamimi, S; Flamini, E; Garetto, S; Lucci, J; Giovagnoni, E; Cinci, L; D’Ambrosio, M; Luceri, C; Ghelardini, C or send Email.

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

A new application aboutMethyl 3-phenyl-2-propenoate

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An article The Role of Support Hydrophobicity in the Selective Hydrogenation of Enones and Unsaturated Sulfones over Cu/SiO2 Catalysts WOS:000546007000067 published article about CHEMOSELECTIVE HYDROGENATION; ALPHA,BETA-UNSATURATED SULFONES; DIHYDROCHALCONES; PALLADIUM; KETONES; RASPBERRY; ALCOHOLS; GINGER; OXIDE in [Cavuoto, Denise] Univ Milan, Dept Chem, Via Golgi 19, I-20133 Milan, Italy; [Cavuoto, Denise; Zaccheria, Federica; Ravasio, Nicoletta] CNR SCITEC, Via C Golgi 19, I-20133 Milan, Italy; [Marelli, Marcello] CNR SCITEC, Via G Fantoli 16-15, I-20138 Milan, Italy; [Evangelisti, Claudio] CNR ICCOM, Via G Moruzzi 1, I-56124 Pisa, Italy; [Piccolo, Oreste] SCSOP, Via Borno 5, I-23896 Sirtori, LC, Italy in 2020.0, Cited 41.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4. Category: esters-buliding-blocks

The substitution of complex hydrides and Ni- and noble metal-based catalysts in the synthesis of pharma and fragrance products is a relevant topic in the green chemistry scenario. Here, we report that non-toxic, non-noble metal-based Cu/SiO(2)catalysts are effective and very selective in the hydrogenation of alpha,beta-unsaturated ketones, esters and sulfones under very mild conditions. Vanillyl acetone can be obtained in quantitative yield in 1 h at 90 degrees C and 1 bar of H-2. High dispersion of the metallic phase and support wettability play a significant role in determining catalytic performance.

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Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Awesome and Easy Science Experiments about Methyl 3-phenyl-2-propenoate

SDS of cas: 103-26-4. Welcome to talk about 103-26-4, If you have any questions, you can contact Knoll, DM; Hu, YL; Hassan, Z; Nieger, M; Brase, S or send Email.

SDS of cas: 103-26-4. I found the field of Biochemistry & Molecular Biology; Chemistry very interesting. Saw the article Planar Chiral [2.2]Paracyclophane-Based Bisoxazoline Ligands and Their Applications in Cu-Mediated N-H Insertion Reaction published in 2019.0, Reprint Addresses Brase, S (corresponding author), Karlsruhe Inst Technol, IOC, Fritz Haber Weg 6, D-76131 Karlsruhe, Germany.; Brase, S (corresponding author), Karlsruhe Inst Technol, ITG, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany.. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate.

New catalysts for important C-N bond formation are highly sought after. In this work, we demonstrate the synthesis and viability of a new class of planar chiral [2.2]paracyclophane-based bisoxazoline (BOX) ligands for the copper-catalyzed N-H insertion of alpha -diazocarbonyls into anilines. The reaction features a wide substrate scope and moderate to excellent yields, and delivers the valuable products at ambient conditions.

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Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics