You Should Know Something about C10H10O2

Application In Synthesis of Methyl 3-phenyl-2-propenoate. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Varela, MT; Ferrarini, M; Mercaldi, VG; Sufi, BD; Padovani, G; Nazato, LIS; Fernandes, JPS or concate me.

An article Coumaric acid derivatives as tyrosinase inhibitors: Efficacy studies through in silico, in vitro and ex vivo approaches WOS:000575792000006 published article about ANTIOXIDANT ACTIVITY; CAFFEIC ACID; MELANOGENESIS; EUGENOL; MELANIN; IMAGE; ESTER in [Varela, Marina Themoteo; Ferrarini, Marcio; Mercaldi, Vitoria Gallo; Fernandes, Joao Paulo S.] Univ Fed Sao Paulo, Inst Environm Chem & Pharmaceut Sci, Dept Pharmaceut Sci, Rua Sao Nicolau 210, BR-09913030 Diadema, SP, Brazil; [Sufi, Bianca da Silva; Padovani, Giovana; Sbrugnera Nazato, Lucas Idacir] Chemyun Quim Ltda, Res & Dev Dept, Av Independencia 1501, BR-18087101 Sorocaba, SP, Brazil in 2020.0, Cited 47.0. Application In Synthesis of Methyl 3-phenyl-2-propenoate. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

p-Coumaric acid is a known inhibitor of tyrosinase, an enzyme involved in the initial steps of the melanin synthesis in human and other species. However, its low lipophilicity impairs its penetration through skin and efficacy as antimelanogenic agent indeed. Accordingly, this paper reports the assessment of several coumaric acid derivatives as tyrosinase inhibitors and antimelanogenic agents in in vitro, in silico and ex vivo assays. The compounds were designed with modifications in the aromatic and acid moieties of p-coumaric acid, being the coumarate esters the most promising derivatives. The compounds showed higher tyrosinase inhibitory activity (pIC(50), 3.7-4.2) than the parent acid, being compounds 1d, 1e and 1f the most potent inhibitors. Docking analysis showed that these esters are competitive inhibitors per se, and act independently of a redox mechanism as suggested by DPPH assays. Moreover, the esters showed efficacy in reducing the melanin deposition in human skin fragments at 0.1% concentration, especially compound le. In summary, there is an important equilibria between tyrosinase affinity and lipophilicity that must be considered to get effective antimelanogenic agents with adequate permeability in the skin.

Application In Synthesis of Methyl 3-phenyl-2-propenoate. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Varela, MT; Ferrarini, M; Mercaldi, VG; Sufi, BD; Padovani, G; Nazato, LIS; Fernandes, JPS or concate me.

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 Dimethyl 5-aminoisophthalate

Formula: C10H11NO4. About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Tang, HJ; Zhang, B; Xue, F; Feng, C or concate me.

Formula: C10H11NO4. I found the field of Chemistry very interesting. Saw the article Visible-Light-Induced Meerwein Fluoroarylation of Styrenes published in 2021, Reprint Addresses Feng, C (corresponding author), Nanjing Tech Univ, Sch Chem & Mol Engn, Tech Inst Fluorochem TIF, Inst Adv Synth, Nanjing 211816, Peoples R China.. The CAS is 99-27-4. Through research, I have a further understanding and discovery of Dimethyl 5-aminoisophthalate.

An unprecedented approach for assembling a broad range of 1,2-diarylethane derivatives with fluorine-containing fully substituted carbon centers was developed. The protocol features straightforward operation, proceeds under metal-free condition, and accommodates a large variety of synthetically useful functionalities. The critical aspect to the success of this novel transformation lies in using aryldiazonium salts as both aryl radical progenitor and also as single electron acceptor which elegantly enables a radical-polar crossover manifold.

Formula: C10H11NO4. About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Tang, HJ; Zhang, B; Xue, F; Feng, C or concate me.

Reference:
Patent; ASTRA ZENECA AB; NPS PHARMACEUTICALS, INC.; WO2004/14881; (2004); A2;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Interesting scientific research on 6H-Benzo[c]chromen-6-one

Name: 6H-Benzo[c]chromen-6-one. About 6H-Benzo[c]chromen-6-one, If you have any questions, you can contact Hauptmann, R; Petrosyan, A; Fennel, F; Cordero, MAA; Surkus, AE; Pospech, J or concate me.

An article Pyrimidopteridine N-Oxide Organic Photoredox Catalysts: Characterization, Application and Non-Covalent Interaction in Solid State WOS:000462057300011 published article about ELECTRON-TRANSFER PROCESS; Z ISOMERIZATION; PHOTOOXIDATIVE DECARBOXYLATION; PHOTOCATALYTIC E; PI INTERACTIONS; ACTIVATION; OXIDATION; CLEAVAGE in [Hauptmann, Richy; Petrosyan, Andranik; Cordero, Miguel A. Argueello; Surkus, Annette-E; Pospech, Jola] Univ Rostock, Leibniz Inst Catalysis, Albert Einstein Str 29a, D-18059 Rostock, Germany; [Fennel, Franziska; Cordero, Miguel A. Argueello] Univ Rostock, Inst Phys, Dynam Mol Syst, Albert Einstein Str 23-24, D-18059 Rostock, Germany in 2019.0, Cited 33.0. Name: 6H-Benzo[c]chromen-6-one. The Name is 6H-Benzo[c]chromen-6-one. Through research, I have a further understanding and discovery of 2005-10-9

Herein we report the photo- and electrochemical characterization of pyrimidopteridine N-oxide-based heterocycles. The potential of their application as organic photoredox catalysts is showcased in the photomediated contra-thermodynamic E -> Z isomerization of cinnamic acid derivatives and oxidative cyclization of 2-phenyl benzoic acid to benzocoumarin using molecular oxygen as a mild oxidant. Furthermore, unprecedented intermolecular non-covalent n-pi-hole interactions in solid state are discussed based on crystallographic and theoretical data.

Name: 6H-Benzo[c]chromen-6-one. About 6H-Benzo[c]chromen-6-one, If you have any questions, you can contact Hauptmann, R; Petrosyan, A; Fennel, F; Cordero, MAA; Surkus, AE; Pospech, J or concate me.

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 Are Children Getting Addicted To Methyl 3-phenyl-2-propenoate

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Cheung, CW; Shen, N; Wang, SP; Ullah, A; Hu, XL; Ma, JA or concate me.. SDS of cas: 103-26-4

SDS of cas: 103-26-4. Recently I am researching about AMIDE BOND FORMATION; PEPTIDE COUPLING REAGENTS; SECONDARY AMIDES; CARBOXYLIC-ACIDS; TRANSAMIDATION; METAL; HYDROAMINATION; ACTIVATION; AMINES, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21225208, 21472137, 21532008]; National Basic Research Program of China (973 Program)National Basic Research Program of China [2014CB745100]; Tianjin University. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Cheung, CW; Shen, N; Wang, SP; Ullah, A; Hu, XL; Ma, JA. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate

Amides are ubiquitous molecules in nature and in synthetic chemistry. Here we report a convenient and efficient method to synthesize N-aryl amides via amidation of esters with nitroarenes. In the presence of manganese metal, this amidation proceeded smoothly without the need for additional catalysts or ligands. Various esters and nitroarenes are suitable substrates to afford a wide range of N-aryl amides, including bio-active molecules and intermediates to drug molecules.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Cheung, CW; Shen, N; Wang, SP; Ullah, A; Hu, XL; Ma, JA or concate me.. SDS of cas: 103-26-4

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

Chemical Properties and Facts of Dimethyl 5-aminoisophthalate

HPLC of Formula: C10H11NO4. About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Zhang, YM; Wang, YC; Guo, YP; Liao, JX; Tu, ZC; Lu, YZ; Ding, K; Tortorella, MD; He, JF or concate me.

An article Identification and synthesis of low-molecular weight cholecystokinin B receptor (CCKBR) agonists as mediators of long-term synaptic potentiation WOS:000459449600014 published article about MEMORY; PLASTICITY; CORTEX; AREA; DESIGN; RAT in [Zhang, Yanmei; Wang, Yican; Guo, Yiping; Liao, Jinxi; Tu, Zhengchao; Lu, Yongzhi; Ding, Ke; Tortorella, Micky D.] Guangzhou Inst Biomed & Hlth, Drug Discovery Pipeline, Guangzhou 510530, Guangdong, Peoples R China; [He, Jufang] Hong Kong Univ Sci & Technol, Div Life Sci, Clearwater Bay, Hong Kong, Peoples R China in 2019, Cited 21. The Name is Dimethyl 5-aminoisophthalate. Through research, I have a further understanding and discovery of 99-27-4. HPLC of Formula: C10H11NO4

Recently, He et al. reported that CCKB receptors located in the neocortex of the brain when bound to their bound natural ligand, CCK peptides, enhance memory, bringing up the possibility that agonists targeting the CCKB receptor may act as therapeutic agents in diseases in which memory loss is marked as observed in dementia and Alzheimer’s. In this report, we describe the synthesis of novel low-molecular weight benzoamine CCKB receptor agonists. The compounds made in this series were determined to be mostly partial agonists, although some antagonists were identified, as well, capable of triggering calcium release in a cell line that overexpresses the CCKB receptor. Compound 35 demonstrated an EC50 of 0.15 mu M in the cell-based assay, but more importantly, several of the compounds, including 35, demonstrated a physiological effect, inducing long-term potentiation in rat brains comparable to the CCK-8 peptide albeit at much higher concentrations. Based on these findings, benzoamines may be the basis for a new series of CCKB receptor agonists in drug-discovery efforts that seek to develop therapeutics to prevent memory loss.

HPLC of Formula: C10H11NO4. About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Zhang, YM; Wang, YC; Guo, YP; Liao, JX; Tu, ZC; Lu, YZ; Ding, K; Tortorella, MD; He, JF or concate me.

Reference:
Patent; ASTRA ZENECA AB; NPS PHARMACEUTICALS, INC.; WO2004/14881; (2004); A2;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Final Thoughts on Chemistry for 6H-Benzo[c]chromen-6-one

Recommanded Product: 6H-Benzo[c]chromen-6-one. About 6H-Benzo[c]chromen-6-one, If you have any questions, you can contact Hanashima, M; Matsumura, T; Asaji, Y; Yoshimura, T; Matsuo, J or concate me.

Recommanded Product: 6H-Benzo[c]chromen-6-one. I found the field of Pharmacology & Pharmacy; Chemistry very interesting. Saw the article Bridged-Selective Intramolecular Diels-Alder Reactions in the Synthesis of Bicyclo[2.2.2]octanes published in 2020.0, Reprint Addresses Matsuo, J (corresponding author), Kanazawa Univ, Grad Sch Med Sci, Div Pharmaceut Sci, Kakuma Machi, Kanazawa, Ishikawa 9201192, Japan.. The CAS is 2005-10-9. Through research, I have a further understanding and discovery of 6H-Benzo[c]chromen-6-one.

Regioselectivity for intramolecular Diels-Alder (IMDA) reactions of 6-acetoxy-6-alkenylcyclohexa-2,4-dien-1-ones that were formed by oxidation of 2-alkenylphenols with lead tetraacetate in acetic acid were studied. Bridged regioselectivity was observed in the IMDA reactions of 6-acetoxy-6-alkenylcyclohexa-2,4-dien-1-ones having a dienophile part which could conjugate with an aromatic group. Bridged seven-and eight-membered rings and bicyclo[2.2.2]octane skeletons were constructed by the present IMDA reactions. Density functional theory (DFT) calculations suggested that conjugation of the dienophile with neighboring aromatic groups lowered the highest occupied molecular orbital-lowest unoccupied molecular orbital (HOMO-LUMO) energy gap and preceded bridged [4 + 2] adducts.

Recommanded Product: 6H-Benzo[c]chromen-6-one. About 6H-Benzo[c]chromen-6-one, If you have any questions, you can contact Hanashima, M; Matsumura, T; Asaji, Y; Yoshimura, T; Matsuo, J or concate me.

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

Chemical Properties and Facts of Methyl 3-phenyl-2-propenoate

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Hajipour, AR; Khorsandi, Z; Abeshtian, Z or concate me.. Formula: C10H10O2

Authors Hajipour, AR; Khorsandi, Z; Abeshtian, Z in ELSEVIER published article about MIZOROKI-HECK; CO; NANOPARTICLES; CHEMISTRY; LIGANDS; HALIDES; OXIDE in [Hajipour, Abdol R.; Khorsandi, Zahra; Abeshtian, Zahra] Isfahan Univ Technol, Dept Chem, Esfahan 84156, Iran; [Hajipour, Abdol R.] Univ Wisconsin, Sch Med, Dept Neurosci, Madison, WI USA in 2019.0, Cited 29.0. Formula: C10H10O2. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

A novel, biodegradable and environmental friendly magnetic cross-linked chitosan fibers and its cobalt complex was prepared and characterized by various techniques such as FT-IR, SEM, EDX, Elemental mapping, TEM, TGA, XRD and VSM analysis. This palladium and phosphine-free catalyst was found as a highly active heterogeneous catalyst for Heck and Sonogashira reactions in green media. The catalyst was easily separated using an external magnet and the recovered catalyst was reused for six cycles without significant loss of catalytic activity.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Hajipour, AR; Khorsandi, Z; Abeshtian, Z or concate me.. Formula: C10H10O2

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

Why do aromatic interactions matter of compound:Methyl 3-phenyl-2-propenoate

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Yang, B; Ying, Y; Zou, J; Ge, SY; Zuo, LH or concate me.. Safety of Methyl 3-phenyl-2-propenoate

An article Comprehensive characterization and quantification of multiple components in Dan-Huang-Qu-Yu capsule using a multivariate data processing approach based on microwave-assisted extraction with UHPLC and Q Exactive quadrupole-orbitrap high-resolution mass spectrometry WOS:000470023400013 published article about LOCATIONS in [Yang, Bo; Ying, Yin; Ge, Shuyu] Tongde Hosp Zhejiang Prov, Dept Pharm, 234 Gucui Rd, Hangzhou 310012, Zhejiang, Peoples R China; [Zuo, Lihua] Zhengzhou Univ, Dept Pharm, Affiliated Hosp 1, Zhengzhou, Henan, Peoples R China; [Zou, Jie] 117th Hosp PLA, Dept Pharm, Hangzhou, Zhejiang, Peoples R China in 2019.0, Cited 20.0. Safety of Methyl 3-phenyl-2-propenoate. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

Dan-Huang-Qu-Yu capsule, a Chinese herbal medicine compound preparation, is widely used for chronic pelvic inflammatory disease. In this study, a rapid, selective, and sensitive microwave-assisted extraction ultra-high-performance liquid chromatography-Q Exactive quadrupole-orbitrap high-resolution mass spectrometry method was developed for analyzing its chemical compositions. A total of 85 compounds, including 22 flavonoids, 8 terpenoids, 5 quinones, 5 phthaleolactone, 23 organic acids, and 22 other compounds were identified from Dan-Huang-Qu-Yu capsule. Among them, 35 major compounds were unambiguously detected by comparing them with reference standards and selected as quality control markers, which were simultaneously determined in Dan-Huang-Qu-Yu capsule. The established method was successfully validated and applied for simultaneous determination of 35 bioactive compounds in Dan-Huang-Qu-Yu capsule from ten sample batches. The quantitative data of the analytes were analyzed by principal component analysis for quality assessment of Dan-Huang-Qu-Yu capsule. Six compounds (e. g., astragaloside IV, salvianolic acid B, ellagic acid, chlorogenic acid, N-butylidenephthalide, and luteolin) were screened out and regarded as chemical markers for quality control of Dan-Huang-Qu-Yu capsule. The established method has been proved to be a novel and useful tool for rapid research of Dan-Huang-Qu-Yu capsule. This research will provide reference for the scientific research of traditional Chinese medicines.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Yang, B; Ying, Y; Zou, J; Ge, SY; Zuo, LH or concate me.. Safety of Methyl 3-phenyl-2-propenoate

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

What unique challenges do researchers face in Methyl 3-phenyl-2-propenoate

Name: Methyl 3-phenyl-2-propenoate. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Zhang, JW; Wang, Y; Feng, YX; Du, SS; Jia, LM or concate me.

An article Contact Toxicity and Repellent Efficacy of Essential Oil from Aerial Parts of Melaleuca bracteata and its Major Compositions against Three Kinds of Insects WOS:000649623700001 published article about CALLOSOBRUCHUS-CHINENSIS L.; INSECTICIDAL ACTIVITIES; CHEMICAL-COMPOSITION; SITOPHILUS-ORYZAE; DERMATOPHAGOIDES-FARINAE; BOTANICAL INSECTICIDES; CONSTITUENTS; BIOACTIVITIES; ANTIOXIDANT; GROWTH in [Zhang, Jiawei; Jia, Liming] Beijing Forestry Univ, Key Lab Silviculture & Conservat, Minist Educ, 35,Tsinghua East Rd, Beijing 100083, Peoples R China; [Wang, Yang; Feng, Yixi; Du, Shushan] Beijing Normal Univ, Fac Geog Sci, Beijing Key Lab Tradit Chinese Med Protect & Util, 19 Xinjiekouwai St, Beijing 100875, Peoples R China; [Jia, Liming] Beijing Forestry Univ, Natl Energy R&D Ctr Nonfood Biomass, 35,Tsinghua East Rd, Beijing 100083, Peoples R China in 2021.0, Cited 56.0. Name: Methyl 3-phenyl-2-propenoate. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

Synthetic insecticides, a traditional tool to avoid the reduction of stored-product due to insects, have emerged a serious of hazards to the environment for years, therefore, botanicals have entered people’s vision. This work aimed to present the essential oil composition of Melaleuca bracteata, and the contact as well as repellent activities against three stored-product insects, i.e. Lasioderma serricorne (Coleoptera: Ptinidae), Tribolium castaneum (Coleoptera: Tenebrionidae), and Sitophilus oryzae (Coleoptera: Curculionidae). For determining the composition, the analysis was performed by GC/FID and GC/MS. Among 11 identified compounds, the principal compounds were methyl eugenol (88.52 %) and methyl cinnamate (7.90 %). The essential oil demonstrated contact toxicity against L. serricorne, T. castaneum, and S. oryzae which LD50 values were 3.2, 22.6, and 20.4 mu g/adult, respectively. Methyl cinnamate was more effective than methyl eugenol. The repellent activity indicated that essential oil and major compositions of M. bracteata were effective against L. serricorne and T. castaneum, but no use for S. oryzae. In the contact assay, L. serricorne showed more sensitivity, however, in repellency assay, T. castaneum was susceptible. We seek to provide a new application of the popular ornamental plant, M. bracteata, and offer an alternative material to botanical insecticides development.

Name: Methyl 3-phenyl-2-propenoate. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Zhang, JW; Wang, Y; Feng, YX; Du, SS; Jia, LM or concate me.

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

Interesting scientific research on Methyl 3-phenyl-2-propenoate

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Niziol, J; Misiorek, M; Ruman, T or concate me.. COA of Formula: C10H10O2

An article Mass spectrometry imaging of low molecular weight metabolites in strawberry fruit (Fragaria x ananassa Duch.) cv. Primoris with Ag-109 nanoparticle enhanced target WOS:000458710000002 published article about AROMA COMPOUNDS; 2,5-DIMETHYL-4-HYDROXY-3(2H)-FURANONE FURANEOL; FLAVOR QUALITY; PHENOLIC-ACIDS; VITAMIN-C; CULTIVARS; PROANTHOCYANIDINS; IDENTIFICATION; BIOSYNTHESIS; ACCUMULATION in [Niziol, Joanna; Misiorek, Maria; Ruman, Tomasz] Rzeszow Univ Technol, Fac Chem, 6 Powstancow Warszawy Ave, PL-35959 Rzeszow, Poland in 2019.0, Cited 98.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4. COA of Formula: C10H10O2

Strawberry (Fragaria x ananassa Duch., Rosaceae) is the subject of many research studies due to its numerous features such as unique taste, aroma and health qualities. The distribution of low molecular weight metabolites belonging to aldehydes, ketones, alcohols, esters, organic acids, phenolics, amino acids and sugars classes within strawberry fruit cross-section was studied using mass spectrometry imaging (MSI) method with Ag-109 nano-particle enhanced target ((AgNPET)-Ag-109). Correlation of distribution of over thirty compounds found in cross-section of strawberry with their biological function is also included.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Niziol, J; Misiorek, M; Ruman, T or concate me.. COA of Formula: C10H10O2

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