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Journal articles on the topic 'Adamantanecarboxylic acid'

Author: Grafiati

Published: 4 June 2025

Last updated: 1 August 2025

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1

Liao, Qi, Lan Jiang, Cong Li, et al. "An Efficient and Practical Method for the Synthesis of Saxagliptin Intermediate 2-(3-Hydroxy-1-adamantane)-2-oxoacetic Acid and Its Optimization." Journal of Chemistry 2019 (October 10, 2019): 1–8. http://dx.doi.org/10.1155/2019/5375670.

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A mild and relatively simple way for preparation of 2-(3-hydroxy-1-adamantane)-2-oxoacetic acid (I) was reported. It was prepared from 1-adamantanecarboxylic acid (II) via sulfuric acid/nitric acid to get 3-hydroxy-1-adamantanecarboxylic acid (III); treated with the one-pot method through acylation, condensation, and decarboxylation to obtain 3-hydroxy-1-acetyladamantane (IV); and finally oxidized by potassium permanganate (KMnO4) to get the target compound (I). The overall yield was about 60%, which provides a new idea for commercial production of saxagliptin intermediate.

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2

Skomorokhov, M. Yu, M. S. Zaborskaya, E. A. Ivleva, A. K. Shiryaev, and Yu N. Klimochkin. "Synthesis of 5,7-dichloro-2-adamantanone." Журнал органической химии 59, no. 3 (2023): 351–57. http://dx.doi.org/10.31857/s0514749223030060.

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The reaction of 2-adamantanecarboxylic acid with an excess of chlorine in the presence of AlCl3 under heating gave 5,7-dichloro-2-adamantanecarboxylic acid. This product was sequentially introduced into the Curtius, deamination, and oxidation reactions to form 5,7-dichloro-2-adamantanone. The resulting product is a key substrate for synthesis of new substances and materials with a set of practically important properties, including both the synthesis of biologically active molecules and systems for chemiluminescent diagnostic methods.

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3

Ortiz de la Morena, Rodrigo, Andika Asyuda, Hao Lu, et al. "Shape controlled assembly of carboxylic acids: formation of a binary monolayer by intercalation into molecular nanotunnels." Physical Chemistry Chemical Physics 22, no. 7 (2020): 4205–15. http://dx.doi.org/10.1039/c9cp06724h.

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4

Schmitz, D., and A. Pich. "Responsive microgels with supramolecular crosslinks: synthesis and triggered degradation in aqueous medium." Polymer Chemistry 7, no. 36 (2016): 5687–97. http://dx.doi.org/10.1039/c6py01039c.

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5

Dikusar1', E. A., N. G. Kozlov, V. I. Potkin, A. P. Yuvchenko, and N. V. Kovganko. "Synthesis of New 1-Adamantanecarboxylic Acid Derivatives." Russian Journal of Organic Chemistry 40, no. 3 (2004): 346–52. http://dx.doi.org/10.1023/b:rujo.0000034968.28257.e9.

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6

Harvey, Pierre D., D. F. R. Gilson, and I. S. Butler. "Phase transitions in adamantane derivatives: adamantanecarboxylic acid." Journal of Physical Chemistry 90, no. 1 (1986): 136–39. http://dx.doi.org/10.1021/j100273a031.

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7

Beake, Edward O. R., Matthew G. Tucker, Martin T. Dove, and Anthony E. Phillips. "Orientational Disorder in Adamantane and Adamantanecarboxylic Acid." ChemPhysChem 18, no. 5 (2017): 459–64. http://dx.doi.org/10.1002/cphc.201601219.

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8

MUNKUEV, A. A., A. ZH SHESHKOVAS, E. V. SUSLOV, K. P. VOLCHO, and N. F. SALAKHUTDINOV. "Optimization of the Synthesis of 2-Adamantanecarboxylic Acid." Химия в интересах устойчивого развития 30, no. 6 (2022): 632–36. http://dx.doi.org/10.15372/khur2022424.

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9

MUNKUEV, A. A., A. ZH SHESHKOVAS, E. V. SUSLOV, K. P. VOLCHO, and N. F. SALAKHUTDINOV. "Optimization of the Synthesis of 2-Adamantanecarboxylic Acid." Chemistry for Sustainable Development 30, no. 6 (2022): 612–16. http://dx.doi.org/10.15372/csd2022424.

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10

Burkhard, Jiří, Josef Janků, and Luděk Vodička. "Reaction of 1-acetyladamantane with thionyl chloride." Collection of Czechoslovak Chemical Communications 53, no. 1 (1988): 110–13. http://dx.doi.org/10.1135/cccc19880110.

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1-Acetyladamantane (I) reacts with thionyl chloride in the presence of pyridine to give 1-(1’-chloroetenyl)adamantane (IV). In the absence of pyridine, the same reaction affords a more complex mixture containing 1-adamantanecarboxylic acid (VI), its ethyl ester (VII), and 1-chloroacetyladamantane (V).

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11

Fukuyama, Takahide, Yu Mukai, and Ilhyong Ryu. "Koch–Haaf reaction of adamantanols in an acid-tolerant hastelloy-made microreactor." Beilstein Journal of Organic Chemistry 7 (September 15, 2011): 1288–93. http://dx.doi.org/10.3762/bjoc.7.149.

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The Koch–Haaf reaction of adamantanols was successfully carried out in a microflow system at room temperature. By combining an acid-tolerant hastelloy-made micromixer, a PTFE tube, and a hastelloy-made microextraction unit, a packaged reaction-to-workup system was developed. By means of the present system, the multigram scale synthesis of 1-adamantanecarboxylic acid was achieved in ca. one hour operation.

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12

Zhu, Hua, Jian Wei Guo, Chu Fen Yang, Sa Liu, Jin Ping Peng, and Yi Hua Cui. "The First Synthesis of N,N,N’,N’-Tetramethyl-1, 3-Disaminomethyl- Adamantane Dihydrochloride." Advanced Materials Research 233-235 (May 2011): 242–45. http://dx.doi.org/10.4028/www.scientific.net/amr.233-235.242.

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A new tertiary amine derivative of adamantane —N,N,N’,N’-tetramethyl-1, 3-disaminomethyl adamantane dihydrochloride (1), which is a key intermediate for preparing Gemini surfactants and bola surfactants, has been synthesized in this paper. The target compound (1) can be synthesized in high yield by using 1-adamantanecarboxylic acid as raw material. The structure of these compounds has been identified.

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13

TOŠNER, ZDENĚK, SAHAR NIKKHOU ASKI та JOZEF KOWALEWSKI. "Rotational Dynamics of Adamantanecarboxylic Acid in Complex with β-cyclodextrin". Journal of Inclusion Phenomena and Macrocyclic Chemistry 55, № 1-2 (2005): 59–70. http://dx.doi.org/10.1007/s10847-005-9019-4.

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14

Krasnikova, Natalia, Sergey Krasnikov, Elizaveta Bolshakova, Polina Koroleva, Anna Nametkina, and Vladimir Yasonov. "Synthesis and characteristics of four new copper(II) carboxylate complexes with adamantane fragment." From Chemistry Towards Technology Step-By-Step 5, no. 1 (2024): 75–84. http://dx.doi.org/10.52957/2782-1900-2024-5-1-75-84.

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The paper considers the results of synthesis, elemental analysis, and spectroscopic methods (IR, UV-vis) of four new copper(II) complexes with anions of 1-adamantanecarboxylic acid, 4-(1-adamantyl)benzoic acid and their L-valine derivatives as ligands. Based on the obtained spectral data, the authors assumed the biyaderic structure of these complexes with bidentate coordination of carboxylate ligands of the type [Cu2+2(RCOO-)4(H2O)2], with RCOO-as carboxylate ligands. The synthesised compounds are of interest as low toxic potential therapeutic agents with anti-inflammatory and anti-cancer acti

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15

Krasnikova, Natalia, Sergey Krasnikov, Elizaveta Bolshakova, Polina Koroleva, Anna Nametkina, and Vladimir Yasonov. "Synthesis and characteristics of four new copper(II) carboxylate complexes with adamantane fragment." From Chemistry Towards Technology Step-By-Step 5, no. 1 (2024): 145–53. http://dx.doi.org/10.52957/2782-1900-2024-5-1-145-153.

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The paper considers the results of synthesis, elemental analysis, and spectroscopic methods (IR, UV-vis) of four new copper(II) complexes with anions of 1-adamantanecarboxylic acid, 4-(1-adamantyl)benzoic acid and their L-valine derivatives as ligands. Based on the obtained spectral data, the authors assumed the biyaderic structure of these complexes with bidentate coordination of carboxylate ligands of the type [Cu2+2(RCOO-)4(H2O)2], with RCOO-as carboxylate ligands. The synthesised compounds are of interest as low toxic potential therapeutic agents with anti-inflammatory and anti-cancer acti

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16

Taulier, Nicolas, та Tigran V. Chalikian. "γ-Cyclodextrin Forms a Highly Compressible Complex with 1-Adamantanecarboxylic Acid". Journal of Physical Chemistry B 112, № 31 (2008): 9546–49. http://dx.doi.org/10.1021/jp8036389.

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17

MORIYA, Yoshio, Mikio SUGAI, Yozo OHSHIMA, and Nobuaki OGAWA. "Solvent Extraction of Copper(II) with 1-Adamantanecarboxylic Acid in Benzene." Analytical Sciences 12, no. 3 (1996): 511–13. http://dx.doi.org/10.2116/analsci.12.511.

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18

YAGRUSHKINA, I. N., M. N. ZEMTSOVA, and I. K. MOISEEV. "ChemInform Abstract: Adamantanecarboxylic Acid Chlorides (I) in Synthesis of Halosubstituted Adamantanes." ChemInform 27, no. 12 (2010): no. http://dx.doi.org/10.1002/chin.199612099.

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19

Bélanger-Gariépy, Francine, François Brisse, Pierre D. Harvey, Denis F. R. Gilson, and Ian S. Butler. "The crystal and molecular structures of adamantanecarboxylic acid at 173 and 280 K." Canadian Journal of Chemistry 68, no. 7 (1990): 1163–69. http://dx.doi.org/10.1139/v90-179.

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The crystal structure of adamantanecarboxylic acid, tricyclo[3.3.1.13,7] decan-1-carboxylic acid C10H15COOH, has been determined by X-ray diffraction at two temperatures, 173 and 280 K. At both temperatures, the unit cells are triclinic, space group[Formula: see text], and each contains two molecules. At 173 K, a = 6.452(3), b = 6.681(2), c = 11.510(3) Å, α = 80.84(2)°, β = 87.22(3)°, γ = 74.11(3)°; V = 471.10 Å3, Dx = 1.271 g cm−3, [Formula: see text]. The structure was solved by direct-methods. The least-squares refinement, based on 1347 observed reflections converged to R = 0.0485 and Rw =

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20

Kawahata, Masatoshi, Kiyoe Matsui, Tadashi Hyodo, Masahide Tominaga, and Kentaro Yamaguchi. "Inclusion and selectivity of amides by p-terphenyl derivative bearing adamantanecarboxylic acid." Tetrahedron 74, no. 49 (2018): 7089–94. http://dx.doi.org/10.1016/j.tet.2018.10.043.

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21

Wu, Guangcheng, Tianyu Jiao, and Hao Li. "Self-Assembly of a Purely Organic Bowl in Water via Acylhydrazone Formation." Molecules 28, no. 3 (2023): 976. http://dx.doi.org/10.3390/molecules28030976.

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A bowl-shaped molecule can be self-assembled by condensing a triscationic hexaaldehyde compound and three equiv. of a dihydrazide linkers in pure water. The molecular bowl is thus composed of a triscationic π-electron deficient platform, as well as a hexagonal rim that contains six acylhydrazone functions. When the counteranions are chloride, the solid-state structure reveals that this molecular bowl undergoes dimerization via N–H···Cl hydrogen bonds, forming a cage-like dimer with a huge inner cavity. This molecular bowl can employ its cavity to accommodate a hydrophobic guest, namely 1-adama

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22

Pavlov, Dmitry, Taisiya Sukhikh, Evgeny Filatov, and Andrei Potapov. "Facile Synthesis of 3-(Azol-1-yl)-1-adamantanecarboxylic Acids—New Bifunctional Angle-Shaped Building Blocks for Coordination Polymers." Molecules 24, no. 15 (2019): 2717. http://dx.doi.org/10.3390/molecules24152717.

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For the first time, orthogonally substituted azole-carboxylate adamantane ligands were synthesized and used for preparation of coordination polymers. The angle-shaped ligands were prepared by the reaction of 1-adamantanecarboxylic acid and azoles (1H-1,2,4-triazole, 3-methyl-1H-1,2,4-triazole, 3,5-dimethyl-1H-1,2,4-triazole, 1H-tetrazole, 5-methyl-1H-tetrazole) in concentrated sulfuric acid. Variation of the solvent and substituents in azole rings allowed to prepare both 1D and 2D copper(II) and nickel(II) coordination polymers, [Cu2(trzadc)4(H2O)0.7]∙DMF∙0.3H2O, [Cu(trzadc)2(MeOH)]∙MeOH, [Ni(

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23

Kovtun, V. Yu, and V. M. Plakhotnik. "Use of adamantanecarboxylic acid for the modification of drugs and biologically active compounds (review)." Pharmaceutical Chemistry Journal 21, no. 8 (1987): 555–63. http://dx.doi.org/10.1007/bf00759430.

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24

KHIL'CHEVSKII, A. N., V. F. BAKLAN, and V. P. KUKHAR'. "ChemInform Abstract: Reaction of Adamatane, Adamantanecarboxylic Acid and Bicyclo(3.3.1) nonanecarboxylic Acid Derivatives with Acetonitrile in Liquid Bromine." ChemInform 28, no. 18 (2010): no. http://dx.doi.org/10.1002/chin.199718105.

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25

Stroganov, V. F. "Modification of epoxy compositions by adducts based on functional derivatives of adamantanol and adamantanecarboxylic acid." Polymer Science Series D 8, no. 1 (2015): 49–53. http://dx.doi.org/10.1134/s1995421215010153.

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26

Zhang, Ying-Ming, Yong Chen, Zhi-Qiang Li, Nan Li та Yu Liu. "Quinolinotriazole-β-cyclodextrin and its adamantanecarboxylic acid complex as efficient water-soluble fluorescent Cd2+ sensors". Bioorganic & Medicinal Chemistry 18, № 4 (2010): 1415–20. http://dx.doi.org/10.1016/j.bmc.2010.01.024.

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27

McAlpine, Shelli R., та Miguel A. Garcia-Garibay. "Binding Studies of Adamantanecarboxylic Acid and a Naphthyl-Bound β-Cyclodextrin by Variable Temperature1H NMR". Journal of Organic Chemistry 61, № 23 (1996): 8307–9. http://dx.doi.org/10.1021/jo9613794.

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28

BELANGER-GARIEPY, F., F. BRISSE, P. D. HARVEY, D. F. R. GILSON, and I. S. BUTLER. "ChemInform Abstract: The Crystal and Molecular Structures of Adamantanecarboxylic Acid at 173 and 280 K." ChemInform 22, no. 5 (2010): no. http://dx.doi.org/10.1002/chin.199105050.

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29

Paulssen, Julie M., and Lisa M. Gieg. "Biodegradation of 1-adamantanecarboxylic acid by algal-bacterial microbial communities derived from oil sands tailings ponds." Algal Research 41 (August 2019): 101528. http://dx.doi.org/10.1016/j.algal.2019.101528.

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30

Safonova, O. A., I. Ya Korsakova, O. I. Ageeva, et al. "Synthesis and biological activity of 5-(adamant-1-yl)salicylic acid, 3-(4-hydroxyphenyl)adamantanecarboxylic acid and some of their derivatives." Pharmaceutical Chemistry Journal 23, no. 9 (1989): 760–65. http://dx.doi.org/10.1007/bf00764444.

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31

Lee, Dong Hee, Jaewook An, Jihye Oh, and In-Hyeok Park. "Zinc(II) and Copper(II) Complexes of 4-Styrylpyridine and 1-Adamantanecarboxylic Acid: Syntheses, Crystal Structures, and Photopolymerization." Crystals 13, no. 8 (2023): 1226. http://dx.doi.org/10.3390/cryst13081226.

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A combination of 4-styrylpyridine (spy) and 1-adamantanecarboxylic acid (Hadc) was employed in the assembly reactions with Zn(II) and Cu(II) nitrates. The photoreactivity of the products was compared and discussed on the basis of the structure–function relationship. Zinc(II) complex 1 is a trinuclear species of type [Zn3(spy)2(adc)6] in which three zinc(II) atoms are linearly arranged, with two adjacent zinc(II) atoms linked by three bridging carboxylates. Two spy ligands occupy both terminal positions, yielding the overall structure of a six-bladed windmill. Copper(II) complex 2, [Cu(spy)2(ad

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32

Orocz, Marta, Kinga Hartman, Marek Smoluch, Jerzy Silberring, and Przemyslaw Mielczarek. "Fmoc solid-phase synthesis of RF9 optimization with mass spectrometry verification." Current Issues in Pharmacy and Medical Sciences 35, no. 1 (2022): 11–15. http://dx.doi.org/10.2478/cipms-2022-0003.

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Abstract The RF9 compound, which is an antagonist of the FF neuropeptide receptors is used as a therapeutic substance to improve the effectiveness of opioids in the chronic treatment of pain. The purpose of this study was to find the most efficient method of RF9 synthesis. The optimization experiment involved solid-phase peptide synthesis. The Fmoc strategy is based on the usage of the 9-fluorenylmethoxycarbonyl group to block reactive amino groups. Commonly applied RF9 synthesis is based on DIC/HOBt activation of 1-adamantanecarboxylic acid prior to its substitution. The experiments carried o

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33

Sorroza-Martínez, Kendra, Israel González-Méndez, Mireille Vonlanthen та ін. "Guest-Mediated Reversal of the Tumbling Process in Phosphorus-Dendritic Compounds Containing β-Cyclodextrin Units: An NMR Study". Pharmaceuticals 14, № 6 (2021): 556. http://dx.doi.org/10.3390/ph14060556.

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The conformational study of dendritic platforms containing multiple β-cyclodextrin (βCD) units in the periphery is relevant to determine the availability of βCD cavities for the formation of inclusion complexes in aqueous biological systems. In this work, we performed a detailed conformational analysis in D2O, via 1D and 2D NMR spectroscopy of a novel class of phosphorus dendritic compounds of the type P3N3-[O-C6H4-O-(CH2)n-βCD]6 (where n = 3 or 4). We unambiguously demonstrated that a functionalized glucopyranose unit of at least one βCD unit undergoes a 360° tumbling process, resulting in a

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34

Wang, Jian-Wei, Ka-Xi Yu, Xin-Yuan Ji та ін. "Structural Insights into the Host–Guest Complexation between β-Cyclodextrin and Bio-Conjugatable Adamantane Derivatives". Molecules 26, № 9 (2021): 2412. http://dx.doi.org/10.3390/molecules26092412.

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Understanding the host–guest chemistry of α-/β-/γ- cyclodextrins (CDs) and a wide range of organic species are fundamentally attractive, and are finding broad contemporary applications toward developing efficient drug delivery systems. With the widely used β-CD as the host, we herein demonstrate that its inclusion behaviors toward an array of six simple and bio-conjugatable adamantane derivatives, namely, 1-adamantanol (adm-1-OH), 2-adamantanol (adm-2-OH), adamantan-1-amine (adm-1-NH2), 1-adamantanecarboxylic acid (adm-1-COOH), 1,3-adamantanedicarboxylic acid (adm-1,3-diCOOH), and 2-[3-(carbox

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35

Shtemenko, Natalia, Katerina Polokhina, Alexander Golichenko, Svetlana Babiy, and Alexander Shtemenko. "Determination of the anticancer properties of cis- and trans-diadamanthylcarboxylates of dirhenium(III)." ScienceRise: Biological Science, no. 4(25) (December 30, 2020): 8–12. http://dx.doi.org/10.15587/2519-8025.2020.217554.

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The aim of the study. The aim of the work was to investigate in vivo anticancer activity of cis- and trans-diadamanthylcarboxylates of dirhenium(III) alone and together with cisplatin in form of nanobins.Materials and methods. Model of tumor growth, Guerin’s carcinoma; intraperitoneal administration of cisplatin, dirhenium(III) compounds in liposomes and of binary liposomes, containing both cytostatics; volumes and final weights of tumors were measured.Results. In vivo antitumor properties of two dirhenium(III) dicarboxylates with 1-adamantanecarboxylic acid moieties as ligands with cis- (I) a

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36

Zhang, Bolin, Yu Chen, Yongjian Wang, Igor Ying Zhang, and Rongfu Huang. "Utilization of Fe-Ethylenediamine-N,N′-Disuccinic Acid Complex for Electrochemical Co-Catalytic Activation of Peroxymonosulfate under Neutral Initial pH Conditions." Molecules 28, no. 17 (2023): 6290. http://dx.doi.org/10.3390/molecules28176290.

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The ethylenediamine-N,N′-disuccinic acid (EDDS) was utilized to form Fe-EDDS complex to activate peroxymonosulfate (PMS) in the electrochemical (EC) co-catalytic system for effective oxidation of naphthenic acids (NAs) under neutral pH conditions. 1-adamantanecarboxylic acid (ACA) was used as a model compound to represent NAs, which are persistent pollutants that are abundantly present in oil and gas field wastewater. The ACA degradation rate was significantly enhanced in the EC/PMS/Fe(III)-EDDS system (96.6%) compared to that of the EC/PMS/Fe(III) system (65.4%). The addition of EDDS led to t

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37

Todorov, Petar, Stela Georgieva, Desislava Staneva, et al. "Study of Novel Peptides for Antimicrobial Protection in Solution and on Cotton Fabric." Molecules 27, no. 15 (2022): 4770. http://dx.doi.org/10.3390/molecules27154770.

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Some new N- and C-modified biomolecular peptide analogues of both VV-hemorphin-5 and VV-hemorphin-7 with varied amino acids (Cys, Glu, His), 1-adamantanecarboxylic acid, and niacin (nicotinic acid) were synthesized by solid-phase peptide synthesis—Fmoc (9-fluorenylmethoxy-carbonyl) chemistry and were characterized in water solutions with different pH using spectroscopic and electrochemical techniques. Basic physicochemical properties related to the elucidation of the peptide structure at physiological pH have been also studied. The results showed that the interaction of peptide compounds with

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38

Lemmerer, Andreas. "Steric effects in hydrogen bonded columns of salts of benzoic acid and 1-adamantanecarboxylic acid with the cyclic amines CnH2n+1NH2, n = 5, 6, 7, 8 and 12." CrystEngComm 13, no. 8 (2011): 2849. http://dx.doi.org/10.1039/c0ce00749h.

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39

Huang, Yining, Denis F. R. Gilson, Ian S. Butler, and Fred Morin. "Study of molecular motions in the orientationally disordered organic solids 1-bromoadamantane and 1-adamantanecarboxylic acid by carbon-13 NMR spin-lattice relaxation and dipolar dephasing time measurements." Journal of Physical Chemistry 95, no. 6 (1991): 2151–56. http://dx.doi.org/10.1021/j100159a016.

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40

HUANG, Y., D. F. R. GILSON, I. S. BUTLER, and F. MORIN. "ChemInform Abstract: Study of Molecular Motions in the Orientationally Disordered Organic Solids 1-Bromoadamantane and 1-Adamantanecarboxylic Acid by 13C NMR Spin-Lattice Relaxation and Dipolar Dephasing Time Measurements." ChemInform 22, no. 25 (2010): no. http://dx.doi.org/10.1002/chin.199125054.

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41

Kinzyabaeva, Z. S., A. R. Akhmetov, E. V. Borovik, R. A. Baykova, and I. E. Alekhina. "ISOMERIZATION OF FULLEROID C60 CONTAINING AN ADAMANTANE FRAGMENT, INTO METHANOFULLERENE UNDER THE ACTION OF ULTRASOUND." Izvestia Ufimskogo Nauchnogo Tsentra RAN, no. 2 (June 16, 2025): 108–13. https://doi.org/10.31040/2222-8349-2025-0-2-108-113.

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The synthesis of a fullerene derivative conjugated with adamantane is based on an original catalytic selective method for the functionalization of carbon clusters with the participation of diazo compounds, previously devel oped in the laboratory of catalytic synthesis of the Institute of Petrochemistry and Catalysis of the Ufa Federal Research Center of the Russian Academy of Sciences. In the cycloaddition reaction of adamantane derivative hy drazone to fullerene C60 under metal complex catalysis conditions in the presence of Pd(PPh3)2Cl2, a single [5,6] open isomer was obtained: a hexaadduct

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42

Golichenko, A. A., and A. V. Shtemenko. "Cluster rhenium(III) complexes with adamantanecarboxylic acids: Synthesis and properties." Russian Journal of Coordination Chemistry 32, no. 4 (2006): 242–49. http://dx.doi.org/10.1134/s1070328406040038.

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43

Ivleva, E. A., V. S. Gavrilova, and Yu N. Klimochkin. "Synthesis of hydroxy derivatives from adamantanecarboxylic acids in the system MnO2–H2SO4." Russian Journal of Organic Chemistry 52, no. 6 (2016): 785–90. http://dx.doi.org/10.1134/s1070428016060051.

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44

Ivleva, E. A., D. V. Zvereva, and Yu N. Klimochkin. "New Features of the H2SO4–HNO3 System in the Synthesis of Adamantanecarboxylic Acids." Russian Journal of General Chemistry 94, no. 8 (2024): 1905–11. http://dx.doi.org/10.1134/s1070363224080024.

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Ivleva, E. A., M. R. Baimuratov, Yu A. Zhuravleva, et al. "Diesters of adamantanecarboxylic acids as promising components of base stocks for industrial synthetic oils." Petroleum Chemistry 56, no. 9 (2016): 873–75. http://dx.doi.org/10.1134/s0965544116090061.

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Kovalev, V. V., L. M. Alimbarova, E. A. Shokova, and G. S. Katrukha. "Synthesis, antiherpes, and antibacterial activity of N-linked conjugates of eremomycin with adamantanecarboxylic acids." Pharmaceutical Chemistry Journal 43, no. 9 (2009): 485–90. http://dx.doi.org/10.1007/s11094-009-0342-8.

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Stroganov, V. F., and I. V. Stroganov. "An investigation of the effect of adamantanecarboxylic acids on the structure of epoxy polymers by means of X-ray structural and thermomechanical analyses." Polymer Science Series D 7, no. 4 (2014): 265–70. http://dx.doi.org/10.1134/s1995421214040145.

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Dikusar, E. A., N. G. Kozlov, V. I. Potkin, A. P. Yuvchenko, and N. V. Kovganko. "Synthesis of New 1-Adamantanecarboxylic Acid Derivatives." ChemInform 35, no. 42 (2004). http://dx.doi.org/10.1002/chin.200442082.

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Purygin, P. P., and V. A. Ermokhin. "Synthesis of Amides of 1-Adamantanecarboxylic Acid." ChemInform 34, no. 32 (2003). http://dx.doi.org/10.1002/chin.200332060.

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HARVEY, P. D., D. F. R. GILSON, and I. S. BUTLER. "ChemInform Abstract: Phase Transitions in Adamantane Derivatives: 1-Adamantanecarboxylic Acid." Chemischer Informationsdienst 17, no. 19 (1986). http://dx.doi.org/10.1002/chin.198619087.

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