Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1976 1
2005 1
2006 1
2007 1
2008 1
2009 1
2010 1
2011 2
2012 2
2018 3
2019 1
2021 1
2022 1
2023 1
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

18 results

Results by year

Filters applied: . Clear all
Page 1
RIFM fragrance ingredient safety assessment, ethyl benzoylacetate, CAS registry number 94-02-0.
Api AM, Belsito D, Botelho D, Bruze M, Burton GA Jr, Cancellieri MA, Chon H, Dagli ML, Dekant W, Deodhar C, Fryer AD, Jones L, Joshi K, Kumar M, Lapczynski A, Lavelle M, Lee I, Liebler DC, Moustakas H, Muldoon J, Penning TM, Ritacco G, Romine J, Sadekar N, Schultz TW, Selechnik D, Siddiqi F, Sipes IG, Sullivan G, Thakkar Y, Tokura Y. Api AM, et al. Food Chem Toxicol. 2024 Mar;183 Suppl 1:114310. doi: 10.1016/j.fct.2023.114310. Epub 2023 Dec 4. Food Chem Toxicol. 2024. PMID: 38056815 No abstract available.
A novel 7α-hydroxysteroid dehydrogenase: Magnesium ion significantly enhances its activity and thermostability.
Ji S, Pan Y, Zhu L, Tan J, Tang S, Yang Q, Zhang Z, Lou D, Wang B. Ji S, et al. Int J Biol Macromol. 2021 Apr 30;177:111-118. doi: 10.1016/j.ijbiomac.2021.02.082. Epub 2021 Feb 13. Int J Biol Macromol. 2021. PMID: 33592267
The specific activities of J-1-1 toward TCDCA, glycochenodeoxycholic acid (GCDCA) and ethyl benzoylacetate (EBA) were 188.3 0.2, 217.6 0.4, and 20.0 0.2 U.mg(-1), respectively, in 50 mM Glycine-NaOH, pH 10.5. ...
The specific activities of J-1-1 toward TCDCA, glycochenodeoxycholic acid (GCDCA) and ethyl benzoylacetate (EBA) were 188.3 0. …
β-Phenylalanine Ester Synthesis from Stable β-Keto Ester Substrate Using Engineered ω-Transaminases.
Buß O, Voss M, Delavault A, Gorenflo P, Syldatk C, Bornscheuer U, Rudat J. Buß O, et al. Molecules. 2018 May 18;23(5):1211. doi: 10.3390/molecules23051211. Molecules. 2018. PMID: 29783679 Free PMC article.
For this reason, omega-transaminases were tested in this study, which enabled the transamination of the beta-keto ester substrate ethyl benzoylacetate. Therefore, a omega-transaminase library was screened using a coloring o-xylylenediamine assay. ...
For this reason, omega-transaminases were tested in this study, which enabled the transamination of the beta-keto ester substrate ethyl …
Evaluation of the Binding Relationship of the RdRp Enzyme to Novel Thiazole/Acid Hydrazone Hybrids Obtainable through Green Synthetic Procedure.
Al-Humaidi JY, Badrey MG, Aly AA, Nayl AA, Zayed MEM, Jefri OA, Gomha SM. Al-Humaidi JY, et al. Polymers (Basel). 2022 Aug 3;14(15):3160. doi: 10.3390/polym14153160. Polymers (Basel). 2022. PMID: 35956675 Free PMC article.
The combination of the acid hydrazide with bifunctional reagents such as acetylacetone, beta-ketoesters (ethyl acetoacetate and ethyl benzoylacetate) resulted in the formation of pyrazole derivatives. ...
The combination of the acid hydrazide with bifunctional reagents such as acetylacetone, beta-ketoesters (ethyl acetoacetate and ethyl …
The tyrosinase inhibitory effects of isoxazolone derivatives with a (Z)-β-phenyl-α, β-unsaturated carbonyl scaffold.
Kim SJ, Yang J, Lee S, Park C, Kang D, Akter J, Ullah S, Kim YJ, Chun P, Moon HR. Kim SJ, et al. Bioorg Med Chem. 2018 Aug 7;26(14):3882-3889. doi: 10.1016/j.bmc.2018.05.047. Epub 2018 May 31. Bioorg Med Chem. 2018. PMID: 29907470
Compounds 1a-1m, which all possessed the (Z)-beta-phenyl-alpha, beta-unsaturated carbonyl scaffold, were synthesized using a tandem reaction consisting of an isoxazolone ring formation and a Knoevenagel condensation, and three starting materials, ethyl benzoylacetate …
Compounds 1a-1m, which all possessed the (Z)-beta-phenyl-alpha, beta-unsaturated carbonyl scaffold, were synthesized using a tandem reaction …
[Condensation of N-alkyl-o-phenylendiamine with ethyl benzoylacetate].
Pennini R, Tajana A, Nardi D. Pennini R, et al. Farmaco Sci. 1976 Feb;31(2):120-5. Farmaco Sci. 1976. PMID: 1261663 Italian.
By reaction in hot xylene of ethyl benzoylacetate with N-methyl-o-phenylenediamine (I a) and N-benzyl-o-phenylenediamine (I b) three five-membered ring compounds and one seven-membered ring compound were obtained. ...
By reaction in hot xylene of ethyl benzoylacetate with N-methyl-o-phenylenediamine (I a) and N-benzyl-o-phenylenediamine (I b) …
Application of comparative proteome analysis to reveal influence of cultivation conditions on asymmetric bioreduction of beta-keto ester by Saccharomyces cerevisiae.
Lin J, Liu Q, Su E, Wei D, Yang S. Lin J, et al. Appl Microbiol Biotechnol. 2008 Oct;80(5):831-9. doi: 10.1007/s00253-008-1602-3. Epub 2008 Aug 5. Appl Microbiol Biotechnol. 2008. PMID: 18679677
Industrial bakers' yeast strain Saccharomyces cerevisiae LH1 was selected for asymmetric reduction of ethyl benzoylacetate to (S)-ethyl 3-hydroxy-3-phenylpropionate. Higher reductive efficiency and higher cofactor availability were obtained with the alternation of c …
Industrial bakers' yeast strain Saccharomyces cerevisiae LH1 was selected for asymmetric reduction of ethyl benzoylacetate to …
Synthetic Strategy for Pyrazolo[1,5-a]pyridine and Pyrido[1,2-b]indazole Derivatives through AcOH and O2-Promoted Cross-dehydrogenative Coupling Reactions between 1,3-Dicarbonyl Compounds and N-Amino-2-iminopyridines.
Behbehani H, Ibrahim HM. Behbehani H, et al. ACS Omega. 2019 Sep 4;4(12):15289-15303. doi: 10.1021/acsomega.9b02430. eCollection 2019 Sep 17. ACS Omega. 2019. PMID: 31552376 Free PMC article.
An efficient method has been developed for the synthesis of uniquely substituted pyrazolo[1,5-a]pyridine and pyrido[1,2-b]indazole derivatives, which involves acetic acid and molecular oxygen promoted cross-dehydrogenative coupling reactions of respective beta-ketoesters and beta …
An efficient method has been developed for the synthesis of uniquely substituted pyrazolo[1,5-a]pyridine and pyrido[1,2-b]indazole derivativ …
Synthesis, Molecular Docking and in Vitro Screening of Some Newly Synthesized Triazolopyridine, Pyridotriazine and Pyridine⁻Pyrazole Hybrid Derivatives.
Flefel EM, El-Sofany WI, El-Shahat M, Naqvi A, Assirey E. Flefel EM, et al. Molecules. 2018 Oct 6;23(10):2548. doi: 10.3390/molecules23102548. Molecules. 2018. PMID: 30301217 Free PMC article.
Further transformation of compound 1 with a different active methylene group, namely acetyl acetone, diethylmalonate, ethyl cyanoacetate, ethyl benzoylacetate and/or ethyl acetoacetate, produced the pyridine-pyrazole hybrid derivatives 11-15. ...
Further transformation of compound 1 with a different active methylene group, namely acetyl acetone, diethylmalonate, ethyl cyanoacetate, …
A short synthesis of the triazolopyrimidine antibiotic essramycin.
Battaglia U, Moody CJ. Battaglia U, et al. J Nat Prod. 2010 Nov 29;73(11):1938-9. doi: 10.1021/np100298m. Epub 2010 Sep 13. J Nat Prod. 2010. PMID: 20836523
A short synthesis of the 1,2,4-triazolo[1,5-a]pyrimidine antibiotic essramycin is described involving condensation of aminoguanidine with ethyl benzoylacetate to give an amino-1,2,4-triazole, followed by condensation with ethyl acetoacetate to form the pyrimidone ri …
A short synthesis of the 1,2,4-triazolo[1,5-a]pyrimidine antibiotic essramycin is described involving condensation of aminoguanidine with …
18 results