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

Author: Grafiati

Published: 4 June 2021

Last updated: 6 February 2022

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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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2

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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3

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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4

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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5

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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6

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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7

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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8

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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9

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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10

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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11

Endo, Katsuya, and Hiroyasu Takahashi. "Synthesis of Novel Peptidomimetics, Cyclic Hexamers of Unnatural Amino Acids, 2,5-Disubstituted 3-Aminobenzoic Acids." HETEROCYCLES 51, no. 2 (1999): 337. http://dx.doi.org/10.3987/com-98-8445.

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12

Dokichev, T. V., D. R. Latypova, R. R. Shakirov, R. Z. Biglova та R. F. Talipov. "Catalyzed synthesis of β-amino acids esters". Russian Journal of Organic Chemistry 46, № 5 (2010): 755–57. http://dx.doi.org/10.1134/s107042801005026x.

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13

Chen, Xiaolan, Lingbo Qu, Wenfeng Li, Jinwei Yuan, and Yufen Zhao. "Synthesis of Phosphoryl Amino Acids Chrysin Esters." Phosphorus, Sulfur, and Silicon and the Related Elements 183, no. 2-3 (2008): 603–9. http://dx.doi.org/10.1080/10426500701793204.

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14

Lynch, Daniel E., Graham Smith, Karl A. Byriel, and Colin H. L. Kennard. "Molecular Cocrystals of Carboxylic Acids. XXVI Adducts of the Amino-Substituted Benzoic Acids with Nitroaromatic Lewis Bases: the Influence of Associative Polyfunctional Substituents on Self-Assembly of Molecules in Cocrystallization Processes." Australian Journal of Chemistry 50, no. 10 (1997): 977. http://dx.doi.org/10.1071/c97067.

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A series of molecular adducts of the isomeric aminobenzoic acids with the nitro-substituted Lewis bases 2-chloro-5-nitropyridine, 5-nitroquinoline and 5-nitroisoquinoline has been prepared and characterized by using infrared spectroscopy and X-ray powder diffraction, and in four cases by single-crystal X-ray diffraction methods. These four compounds are the adducts of 3-aminobenzoic acid with 5-nitroquinoline [(C7H7NO2)(C9H6N2O2)], 4-aminobenzoic acid with 5-nitroquinoline [(C7H7NO2)2(C9H6N2O2)], 2-aminobenzoic acid with 5-nitroisoquinoline [(C7H7NO2)(C9H6N2O2)] and 4-aminobenzoic acid with 5-

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15

Smith, G., DE Lynch, KA Byriel, and CHL Kennard. "Molecular Cocrystals of Carboxylic Acids. XX. The Crystal Structures of 3,5-Dinitrosalicylic Acid and Its Adducts With the Isomeric Monoaminobenzoic Acids." Australian Journal of Chemistry 48, no. 6 (1995): 1133. http://dx.doi.org/10.1071/ch9951133.

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The crystal structure of 3,5-dinitrosalicylic acid monohydrate (1) and its adducts with 2- aminobenzoic acid (2-aba) [( dnsa )(2-aba)] (2), 3-aminobenzoic acid (3-aba) [( dnsa )(3-aba)] (3), and 4-aminobenzoic acid (4-aba) [( dnsa )(4-aba)2] (4), have been determined and the hydrogen bonding associations in each analysed . The acid (1), which is essentially planar, forms strong hydrogen-bonding network associations involving the carboxylic, nitro and phenolic oxygens as well as the lattice water. In all adducts, protonation of the amino group of the second acid occurs, with subsequent hydrogen

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16

Zhao, MJ, D. Robert та L. Jung. "New agents for cutaneous photoprotection: derivatives of α-amino acids, 4-aminobenzoic and 4-methoxycinnamic acids". European Journal of Medicinal Chemistry 28, № 12 (1993): 949–54. http://dx.doi.org/10.1016/0223-5234(93)90050-o.

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17

Tagle, Luis H., Claudio A. Terraza, Alain Tundidor-Camba, and Pablo A. Ortiz. "Silicon-containing oligomeric poly(imido-amides) with amino moieties. Synthesis, characterization and thermal studies." RSC Adv. 4, no. 57 (2014): 30197–210. http://dx.doi.org/10.1039/c4ra04291c.

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Silicon-containing oligomeric poly(imido-amides) (PIAs) were synthesized from dicarboxylic imido-acids containing a Si atom, which were obtained from dianhydrides, amino acids and p-aminobenzoic acid, were polymerized with the diamine bis(4-aminophenyl)diphenylsilane.

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18

Devedjiev, Ivan T., Stanislav G. Bairyamov, and Vladimira S. Videva. "Biomimetic synthesis of esters of natural amino acids." Heteroatom Chemistry 19, no. 3 (2008): 252–55. http://dx.doi.org/10.1002/hc.20427.

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19

MEDVEDKIN, VIACHESLAV N., LIUBOV N. KLIMENKO, YURI V. MITIN, et al. "p-Chlorotetrafluorophenyl esters of N-protected amino acids." International Journal of Peptide and Protein Research 44, no. 5 (2009): 477–84. http://dx.doi.org/10.1111/j.1399-3011.1994.tb00185.x.

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20

Vasil’ev, Yury V., Benjamin J. Figard, Douglas F. Barofsky, and Max L. Deinzer. "Resonant electron capture by some amino acids esters." International Journal of Mass Spectrometry 268, no. 2-3 (2007): 106–21. http://dx.doi.org/10.1016/j.ijms.2007.07.006.

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21

Froussios, Cleanthis, та Miltiadis Kolovos. "Preparation of Diphenylmethyl Esters and Ethers of Unprotected Amino Acids and β-Hydroxy-α-amino Acids". Synthesis 1987, № 12 (1987): 1106–8. http://dx.doi.org/10.1055/s-1987-28185.

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22

Topyazyan, V. O., D. A. Gerasimyan, A. S. �dilyan, and L. O. Mndzhoyan. "Choline esters of n-substituted amino acids II. Synthesis of dialkylaminoalkyl esters of N-substituted ?,?-dehydroamino acids." Pharmaceutical Chemistry Journal 20, no. 6 (1986): 389–92. http://dx.doi.org/10.1007/bf00758331.

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23

Uglea, Constantin V., and Cristinel V. Zǎnoagǎ. "Transport of amino acids through organic liquid membranes. I. p-Aminobenzoic acid." Journal of Membrane Science 47, no. 3 (1989): 285–92. http://dx.doi.org/10.1016/s0376-7388(00)83081-1.

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24

Topuzyan, V. O., G. Yu Khachvakyan, L. V. Shakhbazyan та D. A. Gerasimyan. "Choline esters of N-substituted amino acids. IX. Synthesis and cholinergic properties of β-dimethylaminoethyl esters of N-substituted amino acids". Pharmaceutical Chemistry Journal 31, № 1 (1997): 23–26. http://dx.doi.org/10.1007/bf02464680.

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25

ZHAO, M. J., D. ROBERT та L. JUNG. "ChemInform Abstract: New Agents for Cutaneous Photoprotection: Derivatives of α-Amino Acids, 4-Aminobenzoic and 4-Methoxycinnamic Acids." ChemInform 25, № 13 (2010): no. http://dx.doi.org/10.1002/chin.199413232.

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26

Dokichev, T. V., D. R. Latypova, R. R. Shakirov, R. Z. Biglova та R. F. Talipov. "ChemInform Abstract: Catalyzed Synthesis of β-Amino Acids Esters." ChemInform 41, № 48 (2010): no. http://dx.doi.org/10.1002/chin.201048044.

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27

Csanàdy, G., and K. Medzihradszky. "A CONVENIENT SYNTHESIS OFt-BUTYL ESTERS OF AMINO ACIDS." Organic Preparations and Procedures International 20, no. 2 (1988): 180–84. http://dx.doi.org/10.1080/00304948809355805.

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28

Lee, Yoon-Sik, and Dong-Sik Shin. "Synthesis of Pentafluorophenyl Esters of Nitroveratryloxycarbonyl-Protected Amino Acids." Synlett 2009, no. 20 (2009): 3307–10. http://dx.doi.org/10.1055/s-0029-1218369.

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29

Zicane, D., I. Ravinya, Z. Tetere, I. Rijkure, E. Gudriniece, and U. Kalejs. "Exotic amino acids. 4. Synthesis of methyl esters of some N-heteroamino-methylenemalonic acids." Chemistry of Heterocyclic Compounds 36, no. 6 (2000): 754–57. http://dx.doi.org/10.1007/bf02297688.

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30

Forman, Grant S., Adrian Scaffidi та Robert V. Stick. "An Alternative Synthesis of Some Carbohydrate α-Amino Acids". Australian Journal of Chemistry 57, № 1 (2004): 25. http://dx.doi.org/10.1071/ch03214.

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Several carbohydrate ketones have been converted into their trichloromethyl-branched tertiary alcohols. A subsequent treatment of these alcohols under Corey–Link conditions (base, sodium azide, methanol) has given rise to α-azido esters, transformable into azido acids, amino esters, and amino acids. An amino ester and an azido acid have been coupled to form a dipeptide.

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31

Liu, Yang-Sheng, та You-Yuan Dai. "Distribution Behavior of α-Amino Acids and Aminobenzoic Acid by Extraction with Trioctylamine". Separation Science and Technology 38, № 5 (2003): 1217–28. http://dx.doi.org/10.1081/ss-120018131.

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32

Suresh Babu, Vommina V., та Hosahudya N. Gopi. "Synthesis of β-amino acids using Boc-/Z-amino acid pentafluorophenyl esters". Letters in Peptide Science 6, № 2-3 (1999): 173–78. http://dx.doi.org/10.1007/bf02443633.

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33

Shtrumfs, B., J. Hermane, I. Kalvinsh, and P. Trapencieris. "Unnatural amino acids. 3. Aziridinyl ketones from esters and amides of aziridine-2-carboxylic acids." Chemistry of Heterocyclic Compounds 43, no. 2 (2007): 169–74. http://dx.doi.org/10.1007/s10593-007-0028-7.

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34

Matteson, Donald S., and Ellen C. Beedle. "A directed chiral synthesis of amino acids from boronic esters." Tetrahedron Letters 28, no. 39 (1987): 4499–502. http://dx.doi.org/10.1016/s0040-4039(00)96547-x.

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35

Lee, Sunwoo, Neil A. Beare та John F. Hartwig. "Palladium-Catalyzed α-Arylation of Esters and Protected Amino Acids". Journal of the American Chemical Society 123, № 34 (2001): 8410–11. http://dx.doi.org/10.1021/ja016032j.

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36

Romanova, Nelly N., Alexander G. Gravis та Yurii G. Bundel'. "Michael synthesis of esters of β-amino acids: stereochemical aspects". Russian Chemical Reviews 65, № 12 (1996): 1083–92. http://dx.doi.org/10.1070/rc1996v065n12abeh000244.

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37

Addario, Vincenzo, Yuzhu Guo, Ivan K. Chu, et al. "Proton affinities of methyl esters of N-acetylated amino acids." International Journal of Mass Spectrometry 219, no. 1 (2002): 101–14. http://dx.doi.org/10.1016/s1387-3806(02)00564-x.

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38

Chun, Stephanie W., та Alison R. H. Narayan. "Biocatalytic, Stereoselective Deuteration of α-Amino Acids and Methyl Esters". ACS Catalysis 10, № 13 (2020): 7413–18. http://dx.doi.org/10.1021/acscatal.0c01885.

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39

Jain, Dilip, Meena Tripathi, D. V. Kohli, and R. K. Uppadhyay. "Malonyl amino acids and their esters as psychoactive agents I." Archives of Pharmacal Research 15, no. 2 (1992): 184–86. http://dx.doi.org/10.1007/bf02974096.

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40

Almeida, Ana R. R. P., and Manuel J. S. Monte. "Thermodynamic study of phase transitions in methyl esters of ortho- meta- and para-aminobenzoic acids." Journal of Chemical Thermodynamics 53 (October 2012): 100–107. http://dx.doi.org/10.1016/j.jct.2012.04.006.

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41

TOPUZYAN, V. O., G. YU KHACHVANKYAN, L. V. SHAKHBAZYAN та D. A. GERASIMYAN. "ChemInform Abstract: Choline Esters of N-Substituted Amino Acids. Part 9. Synthesis and Cholinergic Properties of β-Dimethylaminoethyl Esters of N-Substituted Amino Acids." ChemInform 28, № 30 (2010): no. http://dx.doi.org/10.1002/chin.199730189.

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42

Lynch, Daniel E., Graham Smith, Karl A. Byriel, and Colin H. L. Kennard. "Molecular Cocrystals of Carboxylic Acids. XXXII The Crystal Structures of the Adducts of 2-Aminobenzothiazole with 3,5-Dinitrobenzoic Acid (Adduct Hydrate) and 3-Aminobenzoic Acid, and 2-Amino-2-thiazoline with 2-Aminobenzoic Acid." Australian Journal of Chemistry 51, no. 7 (1998): 587. http://dx.doi.org/10.1071/c97204.

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Two adducts of 2-aminobenzothiazole and one of 2-amino-2-thiazoline with aromatic carboxylic acids have been synthesized and their X-ray crystal structures determined. These are 2-aminobenzothiazole with 3,5-dinitrobenzoic acid (the 1 : 1 adduct hydrate) (1), and 3-aminobenzoic acid (1 : 1) (2), and 2-amino-2-thiazoline with 2-aminobenzoic acid (1 : 1) (3). Compound (1) is a non-centrosymmetric proton-transfer complex and gave a signal of 0·30 relative to urea when tested for second-order non-linear optical properties. Compound (3) is also a proton-transfer complex but (2) is not.

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43

Zicane, D., I. Ravinya, Z. Tetere, I. Rijkure, E. Gudriniece, and U. Kalejs. "ChemInform Abstract: Exotic Amino Acids. Part 4. Synthesis of Methyl Esters of Some N-Heteroaminomethylenemalonic Acids." ChemInform 32, no. 19 (2001): no. http://dx.doi.org/10.1002/chin.200119084.

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44

Brückner, Hans, та Matthias Langer. "Gas chromatographic separation of stereoisomeric esters of α-amino acids and α-alkyl-α-amino acids on chiral stationary phases". Journal of Chromatography A 542 (січень 1991): 161–72. http://dx.doi.org/10.1016/s0021-9673(01)88756-2.

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45

Shilin, Serhiy, Illya Lenko, Olga Shablykina, and Volodymyr Khilya. "6-Oxyindan-1-ones with amino acid fragments." French-Ukrainian Journal of Chemistry 6, no. 2 (2018): 18–26. http://dx.doi.org/10.17721/fujcv6i2p18-26.

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New indan-1-one derivatives (8 examples) with amino acid fragments were synthesized through the N-acylation of the amino acids by 2-(3-oxo-2,3-dihydro-1H-inden-5-yloxy)acetic acid using the method of activated N-hydroxysuccinimide esters. To obtain corresponding methyl esters (2 examples) two ways were possible: the N-acylation of the amino acid methyl esters by 2-(3-oxo-2,3-dihydro-1-inden-5-yloxy)acetic acid through the activated imidazole derivatives or methylation of the carboxylic function of preformed N-{[(1-oxoindan-6-yl)oxy]acetyl}amino acids.

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46

Ghalia, Mohamed H., Mohamed Abd El-Hamid, Mohamed A. Zweil, Abd El-Galil E. Amr, and Shimaa A. Moafi. "Synthesis and Reactions of New Chiral Linear and Macrocyclic Tetraand Penta-peptide Candidates." Zeitschrift für Naturforschung B 67, no. 8 (2012): 806–18. http://dx.doi.org/10.5560/znb.2012-0116.

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9a A series of linear and macrocyclic pentapeptide derivatives have been prepared via the coupling of pyridine-2,6-dicarboxylic acid (1) or pyridine-2,6-dicarbonyl dichloride (2) with appropriate amino acid methyl esters. The coupling of 1or 2with aminoacid methyl esters gave the corresponding pyridine dipeptide methyl esters 3, which were hydrolyzed with sodium hydroxide to the corresponding acids 4. The latter compounds 4were coupled with other amino acid methyl esters to afford the corresponding tetrapeptide esters 5, which were hydrolyzed with sodium hydroxide to the corresponding acids 6.

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47

Reischl, Gerald, Medhat El-Mobayed, Rudolf Beißwenger, Klaus Regier, Cäcilia Maichle-Mössmer, and Anton Rieker. "Oxidation-Induced Acyl Group Transfer from Hydroquinone Esters to Nucleophiles." Zeitschrift für Naturforschung B 53, no. 7 (1998): 765–73. http://dx.doi.org/10.1515/znb-1998-0717.

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Bivalent oxidation of 3,5-di-tert-butyl-hydroquinone monoesters leads to phenoxenium ions, which can transfer an acyl group to nucleophiles. Based on this principle, dipeptides, glyco-amino acids and N-sulfonyl-amino acids were synthesized from hydroquinone esters of amino acids and p-toluenesulfonic acid. For this reaction, direct anodic and indirect mediated oxidation, as well as chemical oxidation with NBS or trisarylammoniumyl salts, was used. The mechanism of the acyl transfer is discussed in terms of a direct and/or a mediated process. A spirocyclic key intermediate was isolated and its

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48

Pudhom, Khanitha, and Tirayut Vilaivan. "Synthesis of aryl esters of protected amino acids from aryl sulfonates." Tetrahedron Letters 40, no. 32 (1999): 5939–42. http://dx.doi.org/10.1016/s0040-4039(99)01178-8.

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49

Mokhallalati, Mohamed K., Ming-Jung Wu та Lendon N. Pridgen. "An efficient enantiomeric three step synthesis of β-amino acids (esters)". Tetrahedron Letters 34, № 1 (1993): 47–50. http://dx.doi.org/10.1016/s0040-4039(00)60054-0.

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50

Kolar, Patrik, and Miha Tišler. "A Convenient Synthesis of Substituted Pyrroles from Esters of Amino Acids." Synthetic Communications 24, no. 13 (1994): 1887–93. http://dx.doi.org/10.1080/00397919408010197.

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