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Journal articles on the topic 'Amino-carboxylic'

Author: Grafiati

Published: 1 April 2023

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1

Siutkina, Alena I., Ramiz R. Makhmudov, and Daria A. Shipilovskikh. "Synthesis and analgesic activity evaluation of derivatives of 2-[(1,4-dioxo-1-amino-4-arylbutyl-2-en-2-yl)amino]-4,5,6,7-tetrahydrobenzo[<i>b</i>]thiophene-3-carboxylic acid." Chimica Techno Acta 8, no. 4 (2021): 20218404. http://dx.doi.org/10.15826/chimtech.2021.8.4.04.

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The synthesis of new derivatives of 2-[(1,4-dioxo-1-amino-4-arylbutyl-2-en-2-yl)amino]-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylic acid is described. Starting 2-{[5-aryl-2-oxofuran-3(2H)-ylidene]amino}thiophene-3-carboxylic acids were obtained by intramolecular cyclisation of substituted 4-aryl-4-oxo-2-thienylaminobut-2-enoic acids in acetic anhydride. New derivatives of 2-[(1,4-dioxo-1-amino-4-arylbutyl-2-en-2-yl)amino]-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylic acids were obtained via decyclization reaction of 2-{[5-aryl-2-oxofuran-3(2H)-ylidene]amino}thiophene-3-carboxylic acids.

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2

Кудрявский, Дмитрий Леонович, Елена Константиновна Фомина, Людмила Юльевна Тычинская, Евгений Доминикович Скаковский та Светлана Евгеньевна Богушевич. "NMR spectroscopy of Cu(II) complexes with acrylamide and sodium acrylate copolymer and ω-amino acids". Journal of the Belarusian State University. Chemistry, № 1 (12 квітня 2021): 85–98. http://dx.doi.org/10.33581/2520-257x-2021-1-85-98.

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Macromolecular complexes of acrylamide and sodium acrylate copolymer with microelements, including Cu(II), may form at preparation of crop protection and stimulation compositions, where the copolymer serves as an adhesive, water-retaining and film-forming agent. Preparations for crop production may also contain amino acids that protect plants under stressful conditions (cold, dry, etc.). Carboxylic groups of copolymer, carboxylic and amino groups of amino acids may be involved in mixed Cu(II) ions complexes formation. Number of methylene groups separating carboxylic and amino group of amino ac

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3

Lynch, Daniel E., Tariq Latif, Graham Smith, Karl A. Byriel, Colin H. L. Kennard, and Simon Parsons. "Molecular Cocrystals of Carboxylic Acids. XXXI Adducts of 2-Aminopyrimidine and 3-Amino-1,2,4-triazole with Heterocyclic Carboxylic Acids." Australian Journal of Chemistry 51, no. 5 (1998): 403. http://dx.doi.org/10.1071/c97201.

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A series of molecular adducts of 2-aminopyrimidine and 3-amino-1,2,4-triazole with heterocyclic carboxylic acids have been prepared and characterized by using X-ray powder diffraction and in four cases by single-crystal X-ray diffraction methods. These four compounds are the (1 : 1) adducts of 2-aminopyrimidine with indole-3-acetic acid [(C4H5N3)(C10H9NO2)], N-methylpyrrole-2-carboxylic acid [(C4H5N3)(C6H7NO2)] and thiophen-2-carboxylic acid [(C4H5N3)(C5H4O2S)], and the (1 : 1) adduct of 3-amino-1,2,4-triazole with thiophen-2-carboxylic acid [(C2H4N4)(C5H4O2S)]. Other compounds described are t

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4

Shahmohammadi, Sayeh, Ferenc Fülöp та Enikő Forró. "Efficient Synthesis of New Fluorinated β-Amino Acid Enantiomers through Lipase-Catalyzed Hydrolysis". Molecules 25, № 24 (2020): 5990. http://dx.doi.org/10.3390/molecules25245990.

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An efficient and novel enzymatic method has been developed for the synthesis of β-fluorophenyl-substituted β-amino acid enantiomers through lipase PSIM (Burkholderia cepasia) catalyzed hydrolysis of racemic β-amino carboxylic ester hydrochloride salts 3a–e in iPr2O at 45 °C in the presence of Et3N and H2O. Adequate analytical methods were developed for the enantio-separation of racemic β-amino carboxylic ester hydrochlorides 3a–e and β-amino acids 2a–e. Preparative-scale resolutions furnished unreacted amino esters (R)-4a–e and product amino acids (S)-5a–e with excellent ee values (≥99%) and g

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5

Wermuth, Urs D., Ian D. Jenkins, Raymond C. Bott, Karl A. Byriel, and Graham Smith. "Some Stereochemical Aspects of the Strecker Synthesis and the Bucherer - Bergs Reaction." Australian Journal of Chemistry 57, no. 5 (2004): 461. http://dx.doi.org/10.1071/ch03202.

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Both the Strecker and Bucherer–Bergs reactions convert the norbornane keto ester methyl bicyclo[2.2.1]hept-6-one-2-endo-carboxylate into the lactam 6-endo-aminobicyclo[2.2.1]heptane-2-endo-carboxylic acid-γ-lactam-6-exo-carboxylic acid. This lactam is unusually stable and cannot be hydrolyzed to the corresponding amino acid. The stereochemistry in the Strecker reaction, in which the amino group is endo, is contrary to that expected from literature precedent. The stereochemistry in the Bucherer–Bergs reaction, in which the amino group is also endo, has been confirmed by X-ray crystallographic a

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6

Lynch, Daniel E., Laura J. Nicholls, Graham Smith, Karl A. Byriel, and Colin H. L. Kennard. "Molecular co-crystals of 2-aminothiazole derivatives." Acta Crystallographica Section B Structural Science 55, no. 5 (1999): 758–66. http://dx.doi.org/10.1107/s0108768199003146.

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A series of molecular adducts of 2-aminothiazole derivatives – 2-aminothiazole, 2-amino-2-thiazoline and 2-aminobenzothiazole with the carboxylic-acid-substituted heterocyclics indole-2-carboxylic acid, N-methylpyrrole-2-carboxylic acid and thiophene-2-carboxylic acid – have been prepared and characterized using X-ray powder diffraction and in five cases by single-crystal X-ray diffraction methods. These five compounds are the adducts of 2-amino-2-thiazolium with indole-2-carboxylate [(C3H7N2S)+(C9H6NO2)−], and N-methylpyrrole-2-carboxylate [(C3H7N2S)+-(C6H6NO2)−], 2-aminobenzothiazolium with

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7

Adams, Jerry L., Teng Man Chen, and Brian W. Metcalf. "4-Amino-4,5-dihydrothiophene-2-carboxylic acid." Journal of Organic Chemistry 50, no. 15 (1985): 2730–36. http://dx.doi.org/10.1021/jo00215a027.

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8

LI, JORGE P., TOBIAS O. YELLIN, CHARLES W. DEBROSSE, and DRAKE S. EGGLESTON. "3-Amino-2-piperidinone-6-carboxylic acid." International Journal of Peptide and Protein Research 34, no. 4 (2009): 311–18. http://dx.doi.org/10.1111/j.1399-3011.1989.tb01580.x.

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9

Steinschneider, A., B. Valentine, M. I. Burgar, and D. Fiat. "NMR of carboxylic-17O in amino acids." Magnetic Resonance in Chemistry 23, no. 2 (1985): 104–10. http://dx.doi.org/10.1002/mrc.1260230211.

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10

Moustafa, Moustafa Sherief, Saleh Mohammed Al-Mousawi, Maghraby Ali Selim, Ahmed Mohamed Mosallam, and Mohamed Hilmy Elnagdi. "Organobase-catalyzed three-component reactions for the synthesis of 4H-2-aminopyrans, condensed pyrans and polysubstituted benzenes." Beilstein Journal of Organic Chemistry 10 (January 14, 2014): 141–49. http://dx.doi.org/10.3762/bjoc.10.11.

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Novel routes for the preparation of 2-amino-4H-pyran-3-carbonitrile 9, amino-arylbenzoic acid ester derivatives 13a,b, 2-aminotetrahydro-4H-chromene-3-carbonitrile 18, 3-amino-4-cyanotetrahydronaphthalene-2-carboxylic acid ester 26 and 4-amino-3,5-dicyanophthalic acid ester derivatives 37a–c were developed. The synthetic methods utilize one-pot reactions of acetylene carboxylic acid esters, α,β-unsaturated nitriles and/or active methylenenitriles in the presence of L-proline or DABCO. Plausible mechanisms are suggested for the formation of the products. Finally, these compounds were used for t

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11

Kowalewska, M., H. Kwiecień, M. Śmist, and A. Wrześniewska. "Synthesis of New Benzofuran-2-Carboxylic Acid Derivatives." Journal of Chemistry 2013 (2013): 1–7. http://dx.doi.org/10.1155/2013/183717.

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Novel ethyl ester and methylamide of 5-[bis(2-chloroethyl)amino]-7-methoxybenzofuran-2-carboxylic acid as well as (2-hydroxy-1,1-dimethylethyl)amides of 5-bromo- and 5,7-dichlorobenzofuran-2-carboxylic acid were synthesized and characterized.

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12

Bortoluzzi, Marco, Giulio Bresciani, Fabio Marchetti, Guido Pampaloni та Stefano Zacchini. "MoCl5 as an effective chlorinating agent towards α-amino acids: synthesis of α-ammonium-acylchloride salts and α-amino-acylchloride complexes". Dalton Transactions 44, № 21 (2015): 10030–37. http://dx.doi.org/10.1039/c5dt01002k.

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13

Lynch, Ciarán C., Zeus A. De los Santos, and Christian Wolf. "Chiroptical sensing of unprotected amino acids, hydroxy acids, amino alcohols, amines and carboxylic acids with metal salts." Chemical Communications 55, no. 44 (2019): 6297–300. http://dx.doi.org/10.1039/c9cc02525a.

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Optical chirality sensing of unprotected amino acids, hydroxy acids, amino alcohols, amines and carboxylic acids based on a practical mix-and-measure protocol with readily available copper, iron, palladium, manganese, cerium or rhodium salts is demonstrated.

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14

Kühl, Olaf, Stephan Millinghaus, and Philipp Wehage. "Functionalised, chiral imidazolium compounds from proteinogenic amino acids." Open Chemistry 8, no. 6 (2010): 1223–26. http://dx.doi.org/10.2478/s11532-010-0097-9.

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15

Yin, Dengyang, Xunxiu Hu, Dantong Liu, et al. "Enhanced detection of amino acids in hydrophilic interaction chromatography electrospray tandem mass spectrometry with carboxylic acids as mobile phase additives." European Journal of Mass Spectrometry 23, no. 3 (2017): 98–104. http://dx.doi.org/10.1177/1469066717700643.

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Liquid chromatography coupled with mass spectrometry technique has been widely used in the analysis of biological targets such as amino acids, peptides, and proteins. In this work, eight common single carboxylic acids or diacids, which contain different pKa have been investigated as the additives to the analysis of amino acids. As the results, carboxylic acid additive can improve the signal intensity of acidity amino acids such as Asp and Glu and the chromatographic separation of basic amino acids such as Arg, His, and Lys. In particular, the diacids have better performance than single acids.

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16

Kathiravan, Perumal, Thangavelu Balakrishnan, Perumal Venkatesan, Kandasamy Ramamurthi, María Judith Percino, and Subbiah Thamotharan. "Crystal structure and Hirshfeld surface analysis of 1-carboxy-2-(3,4-dihydroxyphenyl)ethan-1-aminium chloride 2-ammonio-3-(3,4-dihydroxyphenyl)propanoate: a new polymorph ofL-dopa HCl and isotypic with its bromide counterpart." Acta Crystallographica Section E Crystallographic Communications 72, no. 11 (2016): 1628–32. http://dx.doi.org/10.1107/s2056989016016789.

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The title molecular salt, C9H12NO4+·Cl−·C9H11NO4, is isotypic with that of the bromide counterpart [Kathiravanet al.(2016).Acta Cryst.E72, 1544–1548]. The title salt is a second monoclinic polymorph of the L-dopa HCl structure reported earlier in the monoclinic space groupP21[Jandacek & Earle (1971).Acta Cryst.B27, 841–845; Mostad & Rømming (1974).Acta Chemica Scand.B28, 1161–1168]. In the title compound, monoclinic space groupI2, one of the dopa molecules has a positive charge with a protonated α-amino group and the α-carboxylic acid group uncharged, while the second dopa molecule has

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17

Raman, Dr Bhanu, and JunedMunir Shaikh. "SYNTHESIS AND CHARACTERIZATION OF NOVEL AMINO CARBOXYLIC ACIDS." International Journal of Advanced Research 4, no. 12 (2016): 2095–100. http://dx.doi.org/10.21474/ijar01/2626.

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18

Crea, Francesco, Concetta De Stefano, Antonio Gianguzza, Daniela Piazzese, and Silvio Sammartano. "Speciation of poly-amino carboxylic compounds in seawater." Chemical Speciation & Bioavailability 15, no. 3 (2003): 75–86. http://dx.doi.org/10.3184/095422903782775190.

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19

Czekelius, Constantin, and Carl Tzschucke. "Synthesis of Halogenated Carboxylic Acids and Amino Acids." Synthesis 2010, no. 04 (2010): 543–66. http://dx.doi.org/10.1055/s-0029-1218649.

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20

Czekelius, Constantin, and Carl Tzschucke. "Synthesis of Halogenated Carboxylic Acids and Amino Acids." Synthesis 2010, no. 12 (2010): 2110. http://dx.doi.org/10.1055/s-0029-1218805.

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21

Piloto, Ana M., Andrea S. C. Fonseca, Susana P. G. Costa, and M. Sameiro T. Gonçalves. "Carboxylic fused furans for amino acid fluorescent labelling." Tetrahedron 62, no. 39 (2006): 9258–67. http://dx.doi.org/10.1016/j.tet.2006.07.003.

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22

Bacci, M., R. Linari, F. Ricchelli, and B. Salvato. "A new fluorescence from carboxylic and amino acids." Il Nuovo Cimento D 6, no. 5 (1985): 393–404. http://dx.doi.org/10.1007/bf02451898.

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23

Li, Bao Hui. "Chiral Separation of Non-Natural Amide Amino Acid by Capillary Electrophoresis with CD Derivations as Chiral Selective Material." Advanced Materials Research 554-556 (July 2012): 824–27. http://dx.doi.org/10.4028/www.scientific.net/amr.554-556.824.

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A capillary electrophoresis (CE) method for the separation of four kinds of enantiomers of non-natural carboxylic amino acid was built while hydroxypropyl-β- cyclodextrin (HP-β-CD) derivations as chiral selective material. Several different β-CD derivatives were tested for the chiral separation of non-natural carboxylic amino acid, and it was proved that HP-β-CD could show better chiral selectivity. The separation of enantiomers of amino acid was obtained by CE in a 50-μm i.d.×60 cm (effective length 45 cm) fused-silica capillary at 18 kV voltage, while 10 mM phosphate acted as running buffer

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24

Li, Bao Hui, and Bao Juan Tian. "Chiral Separation of Non-Natural Carboxylic Amino Acid by Capillary Electrophoresis with CD Derivations as Chiral Selective Material." Applied Mechanics and Materials 130-134 (October 2011): 4126–29. http://dx.doi.org/10.4028/www.scientific.net/amm.130-134.4126.

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A capillary electrophoresis (CE) method for the separation of four kinds of enantiomers of non-natural carboxylic amino acid was built while hydroxypropyl-β-cyclodextrin (HP-β-CD) derivations as chiral selective material. Several different β-CD derivatives were tested for the chiral separation of non-natural carboxylic amino acid, and it was proved that HP-β-CD could show better chiral selectivity. The separation of enantiomers of amino acid was obtained by CE in a 50-μm i.d.×60 cm (effective length 45 cm) fused-silica capillary at 18 kV voltage, while 10 mM phosphate acted as running buffer a

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25

Reynard, Guillaume, Eve-Marline Joseph-Valcin, and Hélène Lebel. "Protecting-group-free synthesis of hydroxyesters from amino alcohols." Chemical Communications 56, no. 74 (2020): 10938–41. http://dx.doi.org/10.1039/d0cc03242e.

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26

Feng, Zhijing, Carla Castellarin Cudia, Luca Floreano, et al. "A competitive amino-carboxylic hydrogen bond on a gold surface." Chemical Communications 51, no. 26 (2015): 5739–42. http://dx.doi.org/10.1039/c4cc10271a.

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27

Fashina, Adedayo, Edith Antunes, and Tebello Nyokong. "A comparative photophysicochemical study of mono substituted phthalocyanines grafted onto silica nanoparticles." Journal of Porphyrins and Phthalocyanines 18, no. 05 (2014): 396–405. http://dx.doi.org/10.1142/s1088424614500138.

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In this study, we report on the covalent linking of carboxylic acid functionalized silica nanoparticles with zinc phthalocyanine mono-substituted non-peripherally and peripherally with either a 4-amino phenoxy (1, peripheral and 2, non-peripheral) or an amino group (3 peripheral). The grafting is achieved via the formation of an amide bond between the carboxylic acid of the silica nanoparticles and the amino group of the phthalocyanine complexes. The hybrid nanoparticles retained the amorphous nature of silica nanoparticles after conjugation. A slight decrease in fluorescence and a general imp

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28

Truong, Ngoc, Scott J. Sauer, Cyndie Seraphin-Hatcher та Don M. Coltart. "Direct carbon–carbon bond formation via reductive soft enolization: a syn-selective Mannich addition of α-iodo thioesters". Organic & Biomolecular Chemistry 14, № 33 (2016): 7864–68. http://dx.doi.org/10.1039/c6ob01244b.

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29

Kurz, Thomas, and Detlef Geffken. "Synthesis of 3-Amino(alkoxy)-2,4-dioxo-1,3-oxazolidine-5-carboxylates from Tartronic Esters." Zeitschrift für Naturforschung B 54, no. 5 (1999): 667–73. http://dx.doi.org/10.1515/znb-1999-0516.

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The reaction of tartronic esters (1a-d) with 1,1'-carbonyl-di-(1,2,4-triazole), hydrazines or hydroxylamines produces 3-amino/3-alkoxy(aralkoxy)-2,4-dioxo-1,3-oxazolidine-5-carboxylic esters (5,6) which are structurally related to the fungicides Famoxadone (I) and Chlozolinate (II). Under suitable conditions the carboxylic ester of 6 can be converted to a carboxamide (7), carbohydrazide (8) or carbohydroxamic acid (9).

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30

Takagi, Hiroshi, Mika Shichiri, Miho Takemura, Miho Mohri та Shigeru Nakamori. "Saccharomyces cerevisiae Σ1278b Has Novel Genes of the N-Acetyltransferase Gene Superfamily Required for l-Proline Analogue Resistance". Journal of Bacteriology 182, № 15 (2000): 4249–56. http://dx.doi.org/10.1128/jb.182.15.4249-4256.2000.

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ABSTRACT We discovered on the chromosome of Saccharomyces cerevisiae Σ1278b novel genes involved in l-proline analogue l-azetidine-2-carboxylic acid resistance which are not present in the standard laboratory strains. The 5.4 kb-DNA fragment was cloned from the genomic library of thel-azetidine-2-carboxylic acid-resistant mutant derived from a cross between S. cerevisiae strains S288C and Σ1278b. The nucleotide sequence of a 4.5-kb segment exhibited no identity with the sequence in the genome project involving strain S288C. Deletion analysis indicated that one open reading frame encoding a pre

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31

Rajam, Ammaiyappan, Packianathan Thomas Muthiah, Raymond John Butcher, Jerry P. Jasinski, and Jan Wikaira. "Design of two series of 1:1 cocrystals involving 4-amino-5-chloro-2,6-dimethylpyrimidine and carboxylic acids." Acta Crystallographica Section C Structural Chemistry 74, no. 9 (2018): 1007–19. http://dx.doi.org/10.1107/s2053229618009154.

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Two series of a total of ten cocrystals involving 4-amino-5-chloro-2,6-dimethylpyrimidine with various carboxylic acids have been prepared and characterized by single-crystal X-ray diffraction. The pyrimidine unit used for the cocrystals offers two ring N atoms (positions N1 and N3) as proton-accepting sites. Depending upon the site of protonation, two types of cations are possible [Rajam et al. (2017). Acta Cryst. C73, 862–868]. In a parallel arrangement, two series of cocrystals are possible depending upon the hydrogen bonding of the carboxyl group with position N1 or N3. In one series of co

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32

Crossley, MJ, and AW Stamford. "Studies Directed Towards the Total Synthesis of Anticapsin and Related Compounds. III. A Ring-Fragmentation Route to the Anticapsin Skeleton." Australian Journal of Chemistry 47, no. 9 (1994): 1713. http://dx.doi.org/10.1071/ch9941713.

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The α-amino-5-oxo-7-oxabicyclo[4.1.0]heptane-2-propanoic acid framework of anticapsin and related compounds is generated by base-catalysed fragmentation of 2-amino-5,6-epoxy-1-hydroxybicyclo[2.2.2]octane-2-carboxylic acid derivatives in a retro-aldol-like reaction.

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33

Ameen, Mohamed A. "Novel Selective 5-HT3 Receptor Ligands: Facile Generation Methods for 2-Amino- and 4-Aminopyrido[4’,3’:4,5]thieno[2,3-d]pyrimidines." Zeitschrift für Naturforschung B 61, no. 10 (2006): 1234–38. http://dx.doi.org/10.1515/znb-2006-1008.

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This work reports on the synthesis of new 2-amino- and 4-aminopyridothienopyrimidines, with a view to identify potent and selective ligands for the 5-HT3 receptor, starting from derivatives of 2-aminothiophene-3-carboxylic ester, -3-carboxamide, or 2-amino-3-cyanothiophene.

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34

Balaban, R. S., and L. J. Mandel. "Metabolic substrate utilization by rabbit proximal tubule. An NADH fluorescence study." American Journal of Physiology-Renal Physiology 254, no. 3 (1988): F407—F416. http://dx.doi.org/10.1152/ajprenal.1988.254.3.f407.

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The effects of various short-chain fatty acids, carboxylic acids, and amino acids on NADH fluorescence and oxygen consumption (QO2) of rabbit proximal tubule suspensions were determined. The short-chain fatty acids were the most effective substrates in increasing NADH fluorescence and QO2, followed by the carboxylic acids and amino acids. All of the substrates tested that increased NADH fluorescence proportionally increased QO2. This implies that the primary effect of these substrates was to increase QO2 by increasing the delivery of reducing equivalents to NAD and not by stimulating ATP hydro

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35

Michalke, R., K. Taraz, and H. Budzikiewiez. "Azoverdin -an Isopyoverdin." Zeitschrift für Naturforschung C 51, no. 11-12 (1996): 772–80. http://dx.doi.org/10.1515/znc-1996-11-1202.

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For azoverdin, the siderophore of Azomonas macrocytogenes ATCC 12334, a pyoverdintype structure has been suggested. We now present evidence that it is actually an isopyoverdin. Also the sequence of the peptide chain has to be revised. Azoverdin comprises, therefore, the chromophore (3S)-5-amino-1,2-dihydro-8,9-dihydroxy-3H -pyrimido[1,2a]quinoline- 3-carboxylic acid whose amino group is bound to a succinamide residue while the carboxyl group is attached to the N -terminus of L-Hse-[2-(R-1-amino-3-hydroxypropyl)-3,4,5,6- tetrahydropyrimidine-65-carboxylic acid]-N5-acetyl-N5,-hydroxy-ᴅ-Orn-ᴅ-Ser

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36

Pappas, Charalampos G., Andreas G. Tzakos, and Ioannis P. Gerothanassis. "On the Hydration State of Amino Acids and Their Derivatives at Different Ionization States: A Comparative Multinuclear NMR and Crystallographic Investigation." Journal of Amino Acids 2012 (May 14, 2012): 1–11. http://dx.doi.org/10.1155/2012/565404.

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2D, 13C, 14N, and 17O NMR and crystallographic data from the literature were critically evaluated in order to provide a coherent hydration model of amino acids and selected derivatives at different ionization states. 17O shielding variations, longitudinal relaxation times (T1) of 2D and 13C and line widths (Δν1/2) of 14N and 17O, may be interpreted with the hypothesis that the cationic form of amino acids is more hydrated by 1 to 3 molecules of water than the zwitterionic form. Similar behaviour was also observed for N-acetylated derivatives of amino acids. An exhaustive search in crystal stru

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37

Brown, RFC, KJ Coulston, FW Eastwood, and CJ Jurss. "Formation of 4-Nitro-2-phenylquinoline on Attempted Diazotization of 3-Amino-2-phenylquinoline-4-carboxylic Acid." Australian Journal of Chemistry 47, no. 3 (1994): 567. http://dx.doi.org/10.1071/ch9940567.

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38

Radi, Smaail, Chahrazad El Abiad, André P. Carvalho, et al. "An efficient hybrid adsorbent based on silica-supported amino penta-carboxylic acid for water purification." Journal of Materials Chemistry A 6, no. 27 (2018): 13096–109. http://dx.doi.org/10.1039/c8ta02560f.

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39

Umansky, A. B., and A. M. Klyushnikov. "Nickel extraction from hydroxide pulps over amino carboxylic cationites." Izvestiya Vuzov. Tsvetnaya Metallurgiya (Proceedings of Higher Schools. Nonferrous Metallurgy), no. 1 (February 24, 2015): 32. http://dx.doi.org/10.17073/0021-3438-2013-1-32-35.

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40

Zia-ur-Rehman, Muhammad, Mark R. J. Elsegood, Nosheen Akbar, and Rahman Shah Zaib Saleem. "5-Amino-1-phenyl-1H-pyrazole-4-carboxylic acid." Acta Crystallographica Section E Structure Reports Online 64, no. 7 (2008): o1312—o1313. http://dx.doi.org/10.1107/s1600536808018394.

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Avenoza, Alberto, Carlos Cativiela, Miguel A. Fernández-Recio, and Jesús M. Peregrina. "Synthesis of 1-amino-4-hydroxycyclohexane-1-carboxylic acids." Journal of the Chemical Society, Perkin Transactions 1, no. 22 (1999): 3375–79. http://dx.doi.org/10.1039/a904132j.

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Xuan, Richeng, Weixiao Hu, Zhongyu Yang, and Rirong Xuan. "DL-2-Amino-2-thiazoline-4-carboxylic acid trihydrate." Acta Crystallographica Section E Structure Reports Online 59, no. 11 (2003): o1707—o1709. http://dx.doi.org/10.1107/s1600536803022360.

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Keita, Massaba, Rocco De Bona, Mickael Dos Santos, et al. "Access to novel amino trifluoromethyl cyclopropane carboxylic acid derivatives." Tetrahedron 69, no. 15 (2013): 3308–15. http://dx.doi.org/10.1016/j.tet.2013.02.012.

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Wu, Ye, and William Quintana. "Coupling of Amino Carboranes to Carboxylic Acid Containing Substrates." Inorganic Chemistry 38, no. 9 (1999): 2025–29. http://dx.doi.org/10.1021/ic981223h.

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Li, Gong-Chun, Li-Ye Wang, Ran Zhu, and Feng-Ling Yang. "1-Allyl-3-amino-1H-pyrazole-4-carboxylic acid." Acta Crystallographica Section E Structure Reports Online 64, no. 12 (2008): o2264. http://dx.doi.org/10.1107/s1600536808035538.

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Stankovičová, Henrieta, Margita Lácová, Anton Gáplovský, Jarmila Chovancová, and Nad'a Prónayová. "Reaction of 3-formylchromones with aromatic amino carboxylic acids." Tetrahedron 57, no. 16 (2001): 3455–64. http://dx.doi.org/10.1016/s0040-4020(01)00219-8.

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Yamamoto, Yoshinori, та Toshiaki Furuta. "Triethylgallium Mediated Lactamization of α,ω-Amino Carboxylic Acids". Chemistry Letters 18, № 5 (1989): 797–800. http://dx.doi.org/10.1246/cl.1989.797.

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Stoykova, Svetlana A., Anthony Linden та Heinz Heimgartner. "Highly Constrained Linear Oligopeptides Containing Heterocyclicα-Amino Carboxylic Acids". Helvetica Chimica Acta 96, № 9 (2013): 1714–32. http://dx.doi.org/10.1002/hlca.201300062.

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Liu, Jiarong, Ling Liu, Hui Rong, and Xiuhui Zhang. "The potential mechanism of atmospheric new particle formation involving amino acids with multiple functional groups." Physical Chemistry Chemical Physics 23, no. 17 (2021): 10184–95. http://dx.doi.org/10.1039/d0cp06472f.

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