Relevant bibliographies by topics / Esters. Aminobenzoic acids. Amino acids

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Esters. Aminobenzoic acids. Amino acids'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 February 2022

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Journal articles on the topic "Esters. Aminobenzoic acids. Amino acids"

1

Tzimopoulos, Demetrios, Ioannis Sanidas, Anastasia C. Varvogli, et al. "On the bioreactivity of triorganotin aminobenzoates. Investigation of trialkyl and triarylyltin(IV) esters of 3-amino and 4-aminobenzoic acids." Journal of Inorganic Biochemistry 104, no. 4 (2010): 423–30. http://dx.doi.org/10.1016/j.jinorgbio.2009.12.006.

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Wang, Yuan-Yuan, Xiao-Lei Zhao, Hui-Fen Qian, and Wei Huang. "Mono/double 3-methoxypropan-1-amine substituted pyridone azo dyes having isomeric ortho/para-aminobenzoic acids and corresponding methyl esters components." Dyes and Pigments 153 (June 2018): 44–52. http://dx.doi.org/10.1016/j.dyepig.2018.01.054.

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Slobodianiuk, Oksana, Oleksandra Berezhnytska, Tetyana Kamens'ka, and Мария Русакова. "SYNTHESIS AND PROPERTIES OF NEW N-ACYL DERIVATIVES OF ANTHRANILIC ACID." Ukrainian Chemistry Journal 85, no. 4 (2019): 59–70. http://dx.doi.org/10.33609/0041-6045.85.4.2019.59-70.

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A series of N-acyl derivatives of anthranil (or o -aminobenzoic acid) was first synthesized, namely 2-(4-octylbenzamido)benzoic acid, 2-(4-(heptyloxy)- benzamido)benzoic acid, 2-(4-(heptylsulfanyl)benz-amido)benzoic acid. 2-(4-octylbenzamido)benzoic acid was synthesized in five stages of octylbenzene, by acylating chloride acid using a Friedie-Crafts reaction. 2-(4-(heptyloxy)benzamido)benzoic acid was prepared from the methyl ester of p-hydroxybenzoic acid which, at the first stage, was activated with 1-bromoheptane in acetonitrile with potassium carbonate and catalytic amount of sodium iodid
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Cao, Jie, Qi Wang, Jun Mei, and Jing Xie. "Effect of 3-Aminobenzoic Acid Ethyl Ester Methanesulfonate (MS-222) on Quality of Marine Cultured Turbot (Scophthalmus maximus) during Simulated Transport in Water." Fishes 6, no. 2 (2021): 20. http://dx.doi.org/10.3390/fishes6020020.

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This study evaluated the effect of different concentrations (20, 40 and 60 mg/L) of 3-aminobenzoic acid ethyl ester methanesulfonate (MS-222) on the quality changes in turbot during simulated transport in water. The results showed that the ammonia nitrogen content in the transportation water of each sample increased significantly, and the dissolved oxygen level decreased. The dissolved oxygen content in MS-222-treated samples was higher than that of control group (CK) samples. For turbot flesh quality, simulated transport in water led to a decrease in moisture, fat and protein contents in all
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Volkova, Tatiana G., and Irina O. Talanova. "SYNTHESIS AND STUDY OF WATER-SOLUBLE FORMS OF ANAESTHESIN." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 61, no. 6 (2018): 35. http://dx.doi.org/10.6060/tcct.20186106.5661.

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The problem of obtaining highly soluble and biologically active drugs is actual. One of the methods for solving this problem is the inclusion of carbohydrate residues into the structure of biologically active compounds. Ethyl ester of p-(N-α-D-glucopyranoside)aminobenzoic acid has been synthesized by condensation of benzocaine with glucose. The obtained product has been studied by means of NMR spectroscopy, high-performance liquid chromatography and elemental analysis. Comparative analysis of the lipophilic properties of benzocaine and its glycosylated analogue and a profile of the potential t
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Bodanszky, Miklos. "Alkyl Esters of Amino Acids." International Journal of Peptide and Protein Research 23, no. 1 (2009): 111. http://dx.doi.org/10.1111/j.1399-3011.1984.tb02699.x.

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Pietrzak, Marek, Beata Jędrzejewska, Dorota Mądrzejewska, and Agnieszka Bajorek. "Convenient Synthesis of p-Aminobenzoic Acids and their Methyl Esters." Organic Preparations and Procedures International 49, no. 1 (2017): 45–52. http://dx.doi.org/10.1080/00304948.2017.1260396.

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Gevorgyan, G. A., G. Yu Khachvankyan, A. G. Agababyan, N. Z. Akopyan, G. A. Panosyan та M. G. Malakyan. "Synthesis of β-amino ketones derived from aminobenzoic acids". Russian Journal of General Chemistry 87, № 2 (2017): 342–46. http://dx.doi.org/10.1134/s1070363217020311.

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Ito, Amando S., Rozane De F. Turchiello, Isaura Y. Hirata, Maria Helena S. Cezari, Morten Meldal, and Luiz Juliano. "Fluorescent properties of amino acids labeled withortho-aminobenzoic acid." Biospectroscopy 4, no. 6 (1998): 395–402. http://dx.doi.org/10.1002/(sici)1520-6343(1998)4:6<395::aid-bspy4>3.0.co;2-y.

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Suresh Babu, V. V., H. N. Gopi та K. Anandi. "Homologation of α-amino acids to β-amino acids using Fmoc-amino acid pentafluorophenyl esters". Journal of Peptide Research 53, № 3 (1999): 308–13. http://dx.doi.org/10.1034/j.1399-3011.1999.00035.x.

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Dissertations / Theses on the topic "Esters. Aminobenzoic acids. Amino acids"

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Revill, John Austin Timothy. "A study of the solution photophysics of the isomeric aminobenzoic acids, N, N-dimethylaminobenzoic acids and their methyl esters." Thesis, University of Central Lancashire, 1993. http://clok.uclan.ac.uk/20170/.

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The solution photophysics of the isomeric aminobenzoic acids and N,Ndimethylaminobenzoic acids and their methyl esters were studied under a variety of conditions of solvent, pH, concentration and temperature. The most straightforward behaviour was obtained when the amino or N,N-dimethylamino substituent was in the meta- position relative to the carboxylic add or ester function. The amino compounds absorb with a peak between 300 and 325 nm depending on solvent, their fluorescence peaks lie between 350 and 410 rim. The corresponding N,N-dimethylamino compounds usually absorb and fluoresce some 2
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Lao, Hongbai. "A study of the synthesis and properties of some long chain fatty acid esters containing azido, amino, amido and amino acid residues and the analysis of some seed oils used in Chinese medicine /." [Hong Kong : University of Hong Kong], 1989. http://sunzi.lib.hku.hk/hkuto/record.jsp?B12437141.

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老洪柏 and Hongbai Lao. "A study of the synthesis and properties of some long chain fatty acid esters containing azido, amino, amido and amino acid residues and theanalysis of some seed oils used in Chinese medicine." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1989. http://hub.hku.hk/bib/B31208691.

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Chen, Xuan. "Applications of radical reactions for the synthesis of β-amino acids and carbonyl compounds". Thesis, Institut polytechnique de Paris, 2020. http://www.theses.fr/2020IPPAX042.

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Dans cette thèse, nous nous concentrons sur l'application de la chimie des radicaux issus des xanthates pour la synthèse de cétones, d'esters et de dérivés d'acides aminés β2. Cette recherche surmonte de nombreux inconvénients associés à l'alkylation des cétones et des esters lors de l'utilisation de méthodes basées sur l'énolate, et complète la dialkylation des cétones insaturées. Le processus de transfert de xanthate offre également une voie convergente vers des acides aminés potentiellement bioactifs.nous résumons tout d'abord l'utilité et les stratégies de synthèse vis-à-vis des acides ami
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De, Sousa J. A. A. "Kinetic resolution strategies." Thesis, University of Oxford, 1992. http://ora.ox.ac.uk/objects/uuid:46173430-d8b1-44f3-a273-580f9bd1b6bd.

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This thesis is concerned with the use of kinetic resolution strategies for the preparation of enantiomerically pure materials. Chapter 1 introduces kinetic resolution. The limitations of conventional kinetic resolutions are described and the methods used to overcome these limitations are discussed. Chapter 2 presents a double kinetic resolution strategy where the recovered reactant from the first kinetic resolution is used as starting material in a second kinetic resolution. In the second kinetic resolution the major enantiomer present in the starting material is the faster reacting enantiomer
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Loncke, Paul G. "Hydrolytic cleavage of p-nitrophenyl esters of N-protected amino acids in the presence of cyclodextrins : transition state stabilization." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp03/MQ39956.pdf.

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Ji, An. "Mn-mediated radical coupling toward synthesis of alpha, alpha-disubstituted alpha-amino esters and formal synthesis of quinine." Diss., University of Iowa, 2011. https://ir.uiowa.edu/etd/1150.

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Chiral alpha-branched amines are common substructures of bioactive synthetic targets such as alkaloids and amino acids. Direct asymmetric amine synthesis by addition to the C=N bond of carbonyl imino derivatives is promising and efficient to introduce the stereogenic center and carbon-carbon bond in one step. Furthermore, disconnection of either C-C bond at the amine stereogenic center would be the most versatile method to achieve this objective; we could make the choice depending on the different synthetic strategies, such as the availability of precursors and the presence of complicating str
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Ganga, Ramu Vasanthakumar [Verfasser]. "Studies on Chemical Synthesis of Peptides: Efficient Synthetic Methods for β-Amino Acids, Azides, Amino Acid Hydroxamates and Esters : Methodologies in peptide synthesis / Vasanthakumar Ganga Ramu". München : GRIN Verlag, 2011. http://d-nb.info/119000478X/34.

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Kloster, Robin A. "Indane 2,5-diketopiperazine synthons as probes of solid, solution and gas phase supramolecular non-covalent associations: Synthesis, characterization, and analysis of indane amino acids, unnatural bis-amino esters, indane 2,5-diketopiperazines." Diss., The University of Arizona, 2003. http://hdl.handle.net/10150/280299.

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Non-covalent interactions influence supramolecular organization in the solid, solution and gaseous state. While intermolecular forces are well understood individually, it is difficult to predict how their interplay will lead to a highly symmetric and low energy crystalline solid. Analysis, design, and prediction of crystalline architecture is a recently popularized sub-field of supramolecular chemistry referred to as 'crystal engineering'. Crystal engineering seeks to fully understand non-bonding intermolecular forces in order to build crystalline solids that serve some designed purpose. Hydro
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Wang, You Ming, of Western Sydney Hawkesbury University, Faculty of Science and Technology, and School of Science. "The chemistry and biochemistry of melon fruit development and quality." THESIS_FST_SS_Wang_Y.xml, 1994. http://handle.uws.edu.au:8081/1959.7/86.

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A number of methods for the analysis of free amino acids in melon fruit have been evaluated experimentally. Analysis of their tBDMS derivatives by GC (gas chromatography) was found to be the most suitable for the mix of free amino acid found in the melon matrix. It affords good yields of amino acid derivatives with excellent gas chromatographic properties and characteristic mass spectra. The single-step derivatization procedure is highly reproducible and allows simultaneous analysis of asparagine and glutamine together with their corresponding acids. Changes in amino acids, sugars, the princip
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Books on the topic "Esters. Aminobenzoic acids. Amino acids"

1

Michnick, Thomas John. Asymmetric synthesis of acetamido boronic acids and asymmetric synthesis using boronic esters. 1990.

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Book chapters on the topic "Esters. Aminobenzoic acids. Amino acids"

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Toome, Voldemar, and Bogda B. Wegrzynski. "Chiroptical properties of fluorescamine and MDPF condensation compounds with amino acids, amino acid esters and dipeptides." In Amino Acids. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_13.

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North, M. "ROMP of Norbornene Derivatives of Amino-Esters and Amino-Acids." In Ring Opening Metathesis Polymerisation and Related Chemistry. Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0373-5_13.

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Tsuchiya, Kousuke, and Keiji Numata. "Protease-Catalyzed Polymerization of Tripeptide Esters Containing Unnatural Amino Acids: α,α-Disubstituted and N-Alkylated Amino Acids." In Green Polymer Chemistry: New Products, Processes, and Applications. American Chemical Society, 2018. http://dx.doi.org/10.1021/bk-2018-1310.ch007.

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Baev, Alexei K. "Specific Intermolecular Interactions and Energies of Amino Acids and Esters." In Specific Intermolecular Interactions of Nitrogenated and Bioorganic Compounds. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-37472-2_9.

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Fustero, Santos, Juan F. Sanz-Cervera, Julio Piera, María Sánchez-Roselló, Diego Jiménez, and Gema Chiva. "Fluorinated β-Enamino Esters as Versatile Synthetic Intermediates: Synthesis of Fluorinated β-Amino Acids and Uracils." In ACS Symposium Series. American Chemical Society, 2005. http://dx.doi.org/10.1021/bk-2005-0911.ch034.

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Meldal, Morten, and Robert C. Sheppard. "ESTERS OF FMOC-AMINO ACIDS WITH 3,4,-DIHYDRO-3-HYDROXY-4-OXO-1,2,3-BENZOTRIAZINE. A NEW CLASS OF SELF-INDICATING, ACTIVATED INTERMEDIATES FOR SOLID PHASE SYNTHESIS." In Porto Carras, Chalkidiki, Greece, Aug. 31–Sept. 5, 1986, edited by Dimitrios Theodoropoulos. De Gruyter, 1987. http://dx.doi.org/10.1515/9783110864243-027.

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Tidwell, T. T. "β-Amino Acid Esters by Kowalski Homologation of Esters." In Three Carbon-Heteroatom Bonds: Thio-, Seleno-, and Tellurocarboxylic Acids and Derivatives; Imidic Acids and Derivatives; Ortho Acid Derivatives. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-023-00563.

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Smith, M. B. "Direct Cyclization of Amino Acids." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00604.

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Koutentis, P. A., and H. A. Ioannidou. "From α-Amino Acids and Thiocarboxylic Acid Esters." In Science of Synthesis Knowledge Updates KU 2010/4. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-111-00169.

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Beignet, J. "3-Amino-3-oxyalkanoic Acid Esters." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-01323.

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Conference papers on the topic "Esters. Aminobenzoic acids. Amino acids"

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Ullah, Hamid, Andre V. Ferreira, Manoel T. Rodrigues Jr та Fernando Coelho. "Syntheses of β-hydroxy-α-amino esters and non-proteinogenic α-amino acids from Morita-Baylis-Hillman adducts." У 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013819143637.

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Chertov, Oleg, Xiaoying Ye, Timothy Waybright, and Andrew G. Stephen. "Abstract A02: Probing amino acids residues chemical reactivity of KRAS 4b using N-hydroxysuccinimide esters." In Abstracts: AACR Special Conference on Targeting RAS-Driven Cancers; December 9-12, 2018; San Diego, CA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1557-3125.ras18-a02.

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Kulikov, Denis, Ruzaliya Ulanova, and Valentina Kolpakova. "COMPREHENSIVE BIOTECHNOLOGICAL APPROACH TO PROCESSING OF PEA FLOUR FOR FOOD AND FODDER PURPOSES." In GEOLINKS Conference Proceedings. Saima Consult Ltd, 2021. http://dx.doi.org/10.32008/geolinks2021/b1/v3/06.

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Investigations were carried out to optimize the growth parameters of the symbiosis of cultures of the yeast Saccharomyces cerevisiae 121 and the fungus Geotrichum candidum 977 on whey waters formed from pea flour as a secondary product in the production of protein concentrates after precipitation of proteins at the isoelectric point. The whey remaining after protein precipitation is bioconverted at optimal parameters of crop growth (pH of the medium, amount of inoculum, temperature) with the formation of microbial plant concentrate (MPC) for feed purposes. Serum cultures assimilated stachyose,
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Reports on the topic "Esters. Aminobenzoic acids. Amino acids"

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Low, Tammy K., and Eric Enholm. Ring-Closing Metathesis of Macrocyclic Compounds and Cross-Metathesis of Allyl Esters of Amino Acids Leading to Peptidominetics. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada431183.

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