How did you first get involved in researching 6H-Benzo[c]chromen-6-one

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.. SDS of cas: 2005-10-9

SDS of cas: 2005-10-9. In 2020.0 CHEM PHARM BULL published article about TANDEM WESSELY OXIDATION; CYCLOADDITION; ALKALOIDS; ADDITIONS in [Hanashima, Mika; Matsumura, Toshiki; Asaji, Yuta; Yoshimura, Tomoyuki; Matsuo, Jun-ichi] Kanazawa Univ, Grad Sch Med Sci, Div Pharmaceut Sci, Kakuma Machi, Kanazawa, Ishikawa 9201192, Japan in 2020.0, Cited 40.0. The Name is 6H-Benzo[c]chromen-6-one. Through research, I have a further understanding and discovery of 2005-10-9.

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.

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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

What unique challenges do researchers face in 103-26-4

Welcome to talk about 103-26-4, If you have any questions, you can contact Linares, DE; Azuine, RE; Singh, GK or send Email.. Formula: C10H10O2

In 2020.0 J WOMENS HEALTH published article about POSTTRAUMATIC-STRESS-DISORDER; FOOD INSECURITY; POSTPARTUM DEPRESSION; MATERNAL DEPRESSION; UNITED-STATES; PSYCHOSOCIAL PREDICTORS; PERINATAL DEPRESSION; PHYSICAL HEALTH; ABUSE HISTORY; PREGNANCY in [Linares, Deborah E.; Azuine, Romuladus E.] US Hlth Resources & Serv Adm, Div Res, Off Epidemiol & Res, Maternal & Child Hlth Bur,US Dept HHS, Rockville, MD 20857 USA; [Singh, Gopal K.] US Hlth Resources & Serv Adm, Off Hlth Equ, US Dept HHS, Rockville, MD 20857 USA; [Linares, Deborah E.] Natl Inst Minor Hlth & Hlth Dispar, NIH, Two Democracy Plaza,6707 Democracy Blvd,Suite 800, Bethesda, MD 20817 USA in 2020.0, Cited 70.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4. Formula: C10H10O2

Background: Maternal mental illness is a significant public health problem during the perinatal period and beyond. Little is known about how social determinants of health (SDOH) affect maternal mental health. Materials and Methods: We used cross-sectional data from the 2016 to 2017 National Survey of Children’s Health with 19,127 mothers of a nationally representative sample of U.S. children aged 0-5. We estimated the prevalence of poor reported mental health (reported as fair/poor) among mothers with children aged 0-5 by SDOH. Multivariable logistic regression was used to examine factors associated with poor maternal mental health. Results: Approximately 4.5% of mothers with children aged 0-5 reported having poor mental health in 2016-2017. Postadjustment and mothers’ poor mental health were significantly associated with age (adjusted odds ratio [AOR]: 18-20 years: 2.77, 95% confidence interval [CI]: 1.35-5.67; 21-24 years AOR: 2.14, 95% CI: 1.22-3.73, and 30-34 years AOR: 1.97, 95% CI: 1.13-3.43), U.S.-born status (AOR: 2.31, 95% CI: 1.48-3.63), poor physical health (AOR: 8.69, 95% CI: 5.81-13.02), having a child with a special health care need (AOR: 1.65, 95% CI: 1.03-2.64), experiencing food insecurity (afford enough food, yet, unhealthy [AOR: 2.74, 95% CI: 1.59-4.70] and sometimes/often not afford enough food [AOR: 3.20, 95% CI: 1.76-5.84]), and low social capital (AOR: 1.97, 95% CI: 1.04-3.73). Conclusion: Mothers with children aged 0-5 who had poor physical health and experienced food insecurity were at the greatest risk for poor mental health. Integrated perinatal and behavioral health models, screening, and referrals may help identify and treat mothers experiencing these issues.

Welcome to talk about 103-26-4, If you have any questions, you can contact Linares, DE; Azuine, RE; Singh, GK or send Email.. 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

What about chemistry interests you the most C10H11NO4

Bye, fridends, I hope you can learn more about C10H11NO4, If you have any questions, you can browse other blog as well. See you lster.. COA of Formula: C10H11NO4

COA of Formula: C10H11NO4. In 2019 MED CHEM RES 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.

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.

Bye, fridends, I hope you can learn more about C10H11NO4, If you have any questions, you can browse other blog as well. See you lster.. COA of Formula: C10H11NO4

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

What Kind of Chemistry Facts Are We Going to Learn About Methyl 3-phenyl-2-propenoate

Welcome to talk about 103-26-4, If you have any questions, you can contact Fischer, O; Heinrich, MR or send Email.. Recommanded Product: Methyl 3-phenyl-2-propenoate

Recommanded Product: Methyl 3-phenyl-2-propenoate. Authors Fischer, O; Heinrich, MR in WILEY-V C H VERLAG GMBH published article about in [Fischer, Oliver; Heinrich, Markus R.] Friedrich Alexander Univ Erlangen Nurnberg, Dept Chem & Pharm, Pharmaceut Chem, Nikolaus Fiebiger Str 10, D-91058 Erlangen, Germany in 2021.0, Cited 87.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

As a novel Sanger-type reagent, 2-fluoro-5-nitrophenyldiazonium tetrafluoroborate enabled the versatile functionalization of primary and secondary aliphatic alcohols. Based on a mild nucleophilic aromatic substitution of the fluorine atom under unprecedented, base-free conditions, the diazonium unit on the aromatic core of the resulting aryl-alkyl ether could be employed for such diverse transformations as radical C-H activation and cyclization, as well as palladium catalyzed cross-coupling reactions.

Welcome to talk about 103-26-4, If you have any questions, you can contact Fischer, O; Heinrich, MR or send Email.. Recommanded Product: 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

You Should Know Something about 103-25-3

Recommanded Product: Methyl 3-phenylpropionate. Welcome to talk about 103-25-3, If you have any questions, you can contact Liang, WY; Liu, L; Zhou, Q; Yang, D; Lu, Y; Liu, Y or send Email.

Authors Liang, WY; Liu, L; Zhou, Q; Yang, D; Lu, Y; Liu, Y in ELSEVIER published article about PALLADIUM COMPLEXES; DIRECT CARBONYLATION; METHOXYCARBONYLATION; LIGANDS; HYDROESTERIFICATION; STYRENE; EFFICIENT; DIPHOSPHINES; MECHANISM; OLEFINS in [Liang, Wen-Yu; Liu, Lei; Zhou, Qing; Yang, Da; Lu, Yong; Liu, Ye] East China Normal Univ, Sch Chem & Mol Engn, Shanghai Key Lab Green Chem & Chem Proc, 3663 North Zhongshan Rd, Shanghai 200062, Peoples R China in 2020.0, Cited 33.0. Recommanded Product: Methyl 3-phenylpropionate. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3

The Pd-catalyzed alkoxycarbonylation of alkenes using water as a promoter has been scarcely reported before. Herein, water instead of Bronsted/Lewis acid was found to effectively improve the catalytic performance of Pd (MeCN)(2)Cl-2-Xantphos system for alkoxycarbonylation of alkenes. Under the optimal conditions, the best yield of 97% was obtained for the target products (methyl 3-phenylpropanoate and methyl 2-phenylpropanoate) with L/B of 4.3 and TON of 192. With the involvement of water, Pd(MeCN)(2)Cl-2-Xantphos system also exhibited the moderate to good generality to alkoxycarbonylation of different kinds of alkenes with alcohols. The in situ high pressure FT-IR analysis verified that water played an important role in promoting formation and stability of Pd-H active species which was responsible for the efficient alkoxycarbonylation of alkenes. In addition, the ligand effect of Xantphos on this reaction was discussed.

Recommanded Product: Methyl 3-phenylpropionate. Welcome to talk about 103-25-3, If you have any questions, you can contact Liang, WY; Liu, L; Zhou, Q; Yang, D; Lu, Y; Liu, Y or send Email.

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

Extended knowledge of Dimethyl 5-aminoisophthalate

Bye, fridends, I hope you can learn more about C10H11NO4, If you have any questions, you can browse other blog as well. See you lster.. Recommanded Product: 99-27-4

Recommanded Product: 99-27-4. Authors Liu, BW; Zhao, HB; Chen, L; Chen, L; Wang, XL; Wang, YZ in ELSEVIER SCI LTD published article about in [Liu, Bo-Wen; Zhao, Hai-Bo; Chen, Lin; Chen, Li; Wang, Xiu-Li; Wang, Yu-Zhong] Sichuan Univ, Collaborat Innovat Ctr Ecofriendly & Fire Safety, Natl Engn Lab Ecofriendly Polymer Mat Sichuan, Sch Chem Engn,State Key Lab Polymer Mat Engn,MOE, Chengdu 610064, Peoples R China in 2021, Cited 60. The Name is Dimethyl 5-aminoisophthalate. Through research, I have a further understanding and discovery of 99-27-4

Conventional methods to improve the flame retardancy of polymeric materials usually involve the use of flame-retardant elements such as Cl, Br and P, however, their use may bring more smoke and toxic gases hazards, and more importantly, cause non-negligible environmental and ecological problems. In this work, we put forward a novel green strategy that eliminates the use of any conventional flame-retardant elements to improve the flame retardancy by incorporating a synergistically cross-linkable structure (named PN) containing phenylacetylene and phenylimide groups. The resulting PN copolymer exhibited an excellent 55% lower smoke release rate and 68% lower heat release rate than the pure polymer, as well as a high LOI value of 32% and UL-94 V-0 rating with excellent anti-dripping performance. TG-DSC, rheological and FTIR results proved the high cross-linking ability of the PN copolymer due to the synergistic cross-linking effect between the imide-isoimide rearrangement of phenylimide and the self-cross-linking of phenylacetylene. The SEM, Raman and Py-GC/MS results further upheld the condensed phase flame-retardant mechanism. This eco-friendly synergistic cross-linking strategy provided new perspective for the design and synthesis of polymeric materials with excellent flame retardancy, great anti-dripping performance, and low release of heat, smoke, and toxic gas.

Bye, fridends, I hope you can learn more about C10H11NO4, If you have any questions, you can browse other blog as well. See you lster.. Recommanded Product: 99-27-4

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

An overview of features, applications of compound:6H-Benzo[c]chromen-6-one

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.. Formula: C13H8O2

An article Intramolecular Aromatic C-H Acyloxylation Enabled by Iron Photocatalysis WOS:000516667200032 published article about DEHYDROGENATIVE LACTONIZATION; PHOTOREDOX CATALYSIS; CARBOXYLIC-ACIDS; METAL-COMPLEXES; C(SP(2))-H; FUNCTIONALIZATION; DIBENZOPYRANONES; LACTONES; SYSTEM in [Xia, Siqi; Lei, Chuanhu] Shanghai Univ, Coll Sci, Ctr Supramol Chem & Catalysis, Shanghai 200444, Peoples R China; [Xia, Siqi; Lei, Chuanhu] Shanghai Univ, Coll Sci, Dept Chem, Shanghai 200444, Peoples R China; [Xia, Siqi; Hu, Kunjun; Jin, Jian] Chinese Acad Sci, Univ Chinese Acad Sci, Shanghai Inst Organ Chem, CAS Key Lab Synthet Chem Nat Subst,Ctr Excellence, Shanghai 20032, Peoples R China in 2020.0, Cited 73.0. Formula: C13H8O2. The Name is 6H-Benzo[c]chromen-6-one. Through research, I have a further understanding and discovery of 2005-10-9

A mild and efficient protocol for the intramolecular aromatic C-H oxygenation of 2-biphenylcarboxylic acids has been achieved via iron photocatalysis. The 2-biphenylcarboxylic acids with a diverse array of substituents at both phenyl rings could furnish the oxygenation products in good to excellent yields. We speculate that the aryl carboxylate-iron(III) complexes should generate the aroyloxy radicals and iron(II) upon visible light irradiation.

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.. Formula: C13H8O2

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

Welcome to talk about 103-26-4, If you have any questions, you can contact Iakovenko, R; Hlavac, J or send Email.. COA of Formula: C10H10O2

Recently I am researching about HYDROGEN/DEUTERIUM EXCHANGE; 3+2 ANNULATION; ALKENES; VINYL; ACTIVATION; REDUCTION; PALLADIUM; DEUTERIUM; OLEFINS; ARYL, Saw an article supported by the Czech Ministry of Education, Youth, and SportsMinistry of Education, Youth & Sports – Czech Republic [IGA_PrF_2020_012]. COA of Formula: C10H10O2. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Iakovenko, R; Hlavac, J. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate

Various bromophenylalkenes were reductively photodebrominated by using 1,3-dimethyl-2-phenyl-1H-benzo-[d]imidazoline (DMBI) and 9,10-dicyanoanthracene. With deuterated DMBI analogs (the most effective was DMBI-d(11)), satisfactory to excellent isotopic yields were obtained. DMBI-d(11) could also be regenerated from the reaction mixtures with a recovery rate of up to 50%. The combination of the photodebromination reaction with conventional methods for bromoalkene synthesis enables sequential monodeuteration of a double bond without the necessity of a metal catalyst.

Welcome to talk about 103-26-4, If you have any questions, you can contact Iakovenko, R; Hlavac, J or send Email.. 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

Machine Learning in Chemistry about 2005-10-9

Recommanded Product: 6H-Benzo[c]chromen-6-one. 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.

An article Urea-2,2-dihydroperoxypropane as a Novel and High Oxygen Content Alternative to Dihydroperoxypropane in Several Oxidation Reactions WOS:000458164500004 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. Recommanded Product: 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

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.

Recommanded Product: 6H-Benzo[c]chromen-6-one. 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

A new application about103-26-4

Welcome to talk about 103-26-4, If you have any questions, you can contact Zhang, C; Chen, XL; Crandall-Stoder, B; Qian, P; Kollner, TG; Guo, H; Chen, F or send Email.. Product Details of 103-26-4

In 2019 PHYTOCHEMISTRY published article about ESSENTIAL OIL COMPOSITION; BIOCHEMICAL-CHARACTERIZATION; CARBOXYL METHYLTRANSFERASE; ARABIDOPSIS-THALIANA; TERPENE SYNTHASES; INDOLE-3-ACETIC-ACID METHYLTRANSFERASE; SABATH METHYLTRANSFERASES; MOLECULAR-CLONING; VOLATILE; SALICYLATE in [Zhang, Chi; Chen, Xinlu; Chen, Feng] Univ Tennessee, Dept Plant Sci, Knoxville, TN 37996 USA; [Crandall-Stoder, Barbara] Southern Illinois Univ, Dept Plant Biol, Carbondale, IL 62901 USA; [Qian, Ping] Shandong Agr Univ, Chem & Mat Sci Fac, Tai An 271018, Shandong, Peoples R China; [Koellner, Tobias G.] Max Planck Inst Chem Ecol, Dept Biochem, Hans Knoll Str 8, D-07745 Jena, Germany; [Guo, Hong] Univ Tennessee, Dept Biochem Cellular & Mol Biol, Knoxville, TN 37996 USA; [Guo, Hong] Oak Ridge Natl Lab, UT ORNL Ctr Mol Biophys, Oak Ridge, TN 37830 USA in 2019, Cited 63. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4. Product Details of 103-26-4

Methyl (E)-cinnamate is a specialized metabolite that occurs in a variety of land plants. In flowering plants, it is synthesized by cinnamic acid methyltransferase (CAMT) that belongs to the SABATH family. While rarely reported in bryophytes, methyl (E)-cinnamate is produced by some liverworts of the Conocephalum conicum complex, including C. salebrosum. In axenically grown thalli of C. salebrosum, methyl (E)-cinnamate was detected as the dominant compound. To characterize its biosynthesis, six full-length SABATH genes, which were designated CsSABATH1-6, were cloned from C. salebrosum. These six genes showed different levels of expression in the thalli of C. salebrosum. Next, CsSABATH1-6 were expressed in Escherichia coli to produce recombinant proteins, which were tested for methyltransferase activity with cinnamic acid and a few related compounds as substrates. Among the six SABATH proteins, CsSABATH6 exhibited the highest level of activity with cinnamic acid. It was renamed CsCAMT. The apparent Km value of CsCAMT using (E)-cinnamic acid as substrate was determined to be 50.5 mu M. In contrast, CsSABATH4 was demonstrated to function as salicylic acid methyltransferase and was renamed CsSAMT. Interestingly, the CsCAMT gene from a sabinene-dominant chemotype of C. salebrosum is identical to that of the methyl (E)-cinnamate-dominant chemotype. Structure models for CsCAMT, CsSAMT and one flowering plant CAMT (ObCCMT1) in complex with (E)-cinnamic acid and salicylic acid were built, which provided structural explanations to substrate specificity of these three enzymes. In phylogenetic analysis, CsCAMT and ObCCMT1 were in different clades, implying that methyl (E)-cinnamate biosynthesis in bryophytes and flowering plants originated through convergent evolution.

Welcome to talk about 103-26-4, If you have any questions, you can contact Zhang, C; Chen, XL; Crandall-Stoder, B; Qian, P; Kollner, TG; Guo, H; Chen, F or send Email.. Product Details of 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