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Relevant bibliographies by topics / Adamantane-1-acetic acid methyl ester

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Academic literature on the topic 'Adamantane-1-acetic acid methyl ester'

Author: Grafiati

Published: 5 June 2025

Last updated: 2 August 2025

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Journal articles on the topic "Adamantane-1-acetic acid methyl ester"

1

Koshchii, I., Yu. Klimko, and T. Shamota. "ADAMANTANE-1-CARBOXYLIC ACID AS A THIONECARBOXYLIC ACID SYNTHON." POLISH JOURNAL OF SCIENCE, no. 75 (June 18, 2024): 9–18. https://doi.org/10.5281/zenodo.12059312.

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Adamantane-1-carboxylic acid (AdCOOH) is an important chemical compound that can be used in the fields of science and industry. The purpose of the work was a detailed study of adamantane-1-carboxylic acid, its chemical properties and reactivity, in the context of the development of new derivatives.The reaction of adamantane-1-carboxylic acid methyl ester with phosphorus pentasulfide in dimethoxyethane or dioxane was the first to produce adamantane-1-thioncarboxylic acid methyl ester. Its reactions with hydroxylamine and O-methylhydroxylamine lead to the predominant formation of 1-adamantyl cya

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2

D’yachenko, Vladimir, Dmitry Danilov, Yaroslav Kuznetsov, et al. "Synthesis and Properties of 1,3-Disubstituted Ureas Containing (Adamantan-1-yl)(phenyl)methyl Fragment Based on One-Pot Direct Adamantane Moiety Inclusion." Molecules 28, no. 8 (2023): 3577. http://dx.doi.org/10.3390/molecules28083577.

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A one-stage method for the preparation of 1-[isocyanato(phenyl)methyl]adamantane containing a phenylmethylene fragment located between the adamantane fragment and the isocyanate group, and 1-[isocyanato(phenyl)methyl]-3,5-dimethyladamantane with additional methyl groups at the nodal positions of adamantane, with a yield of 95% and 89%, respectively, is described. The method includes the direct inclusion of an adamantane moiety through the reaction of phenylacetic acid ethyl ester with 1,3-dehydroadamantane or 3,5-dimethyl-1,3-dehydroadamantane followed by the hydrolysis of the obtained esters.

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3

Nahar, Lutfun, Satyajit D. Sarker, and Alan B. Turner. "Synthesis of Pregnenolone and Methyl Lithocholate Oxalate Derivatives." Natural Product Communications 3, no. 1 (2008): 1934578X0800300. http://dx.doi.org/10.1177/1934578x0800300106.

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Five new steroidal oxalate derivatives, oxalic acid (pregn-5-en-20-one)-3β-yl ethyl ester (2), oxalic acid mono (pregn-5-en-20-one)-3β-yl ester (3), chloro-oxo-acetic acid (5β-cholan-24-oic acid methyl ester)-3α-yl ester (5), oxalic acid mono (5β-cholan-24-oic acid methyl ester)-3α-yl ester (6) and oxalic acid (5β-cholan-24-oic acid methyl ester)-3α-yl ethyl ester (7) were synthesized, respectively, from pregnenolone (1) and methyl lithocholate (4) using excess oxalyl chloride.

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4

Agudoawu, Sammy A., Sai-hay Yiu, and Edward E. Knaus. "Synthesis of 2-methyl-2-[1-(3-benzoyl-4-phenyl-1,4-dihydropyridyl)]acetic acid methyl ester, acetic acid, and acetamide analogs as potential antiarthritic agents." Canadian Journal of Chemistry 75, no. 8 (1997): 1106–9. http://dx.doi.org/10.1139/v97-131.

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The cuprous iodide catalyzed reaction of 2-methyl-2-[1-(3-benzoyl-4-phenylpyridinium)]acetic acid methyl ester bromide (5), prepared by reaction of 3-benzoylpyridine (4) with racemic methyl 2-bromopropionate, with phenylmagnesium chloride at −23 °C afforded the 2-methyl-2-[1-(3-benzoyl-4-phenyl-1,4-dihydropyridyl)acetic acid methyl ester (6, 74%), which was a mixture of four diastereomers. Recrystallization of this diastereomeric mixture from diethyl ether afforded a solid product (6a-solid, 30%, 4R*,2R* and 4S*,2S*) and an oil product (6b-oil, 39%, 4R*,2S* and 4S*,2R*), each consisting of a m

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5

Valenta, Vladimír, Jiří Holubek, Emil Svátek, and Miroslav Protiva. "Potential cholinergic and anticholinergic compounds: Synthesis of 2,8-substituted 2,8-diazaspiro[4,5]decane-1,3-diones." Collection of Czechoslovak Chemical Communications 55, no. 9 (1990): 2304–16. http://dx.doi.org/10.1135/cccc19902304.

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Heating the ammonium salt of (4-carboxy-1-methyl-4-piperidinyl)acetic acid (XII) gave 8-methyl-2,8-diazaspiro[4,5]decane-1,3-dione (II) which was N-alkylated with 2-bromoethanol and 4-bromobutanol to give the alcohols III and V. Compound III was transformed to the chloro compound VI which was reacted with the sodium salt of hexahydrobenzilic acid to give the ester VII. Compound V was transformed to the 4-toluenesulfonic ester VIII which reacted with 1-(2-pyrimidinyl)piperazine and gave IX. 2-(2-Propyl)-2,8-diazaspiro[4,5]decane-1,3-dione (XVIII) was similarly transformed via XIX to XX which re

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6

Jenan, Mohammed Ubaid, Fauzi Al-Rubaye Abeer, and Hadi Hameed Imad. "Analysis of Bioactive Chemical Compounds of Trogoderma granarium (Insecta: Coleoptera: Dermestidae) Using Gas Chromatography – Mass Spectrometry." International Journal of Toxicological and Pharmacological Research 9, no. 3 (2017): 199–205. https://doi.org/10.5281/zenodo.12698026.

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Methanolic extract of bioactive compounds of <em>Trogoderma granarium</em> was assayed. GC-MS analysis of <em>Trogoderma granarium</em> revealed the existence of the Pentanoic acid , 1,1-dimethylpropyl ester , (1H)-Pyrimidinone , 5-chloro-4,6-diphenyl, Cyclobutanemethanol , α-methyl- , Nitro-2-methyl-1,3-propanediol , Hydroxylamine ,O-(2-methylpropyl)- , Uridine , 2′,3′-O-(phenylmethylene)- ,Acetic acid ,2-benzoylthio-,2-oxo-2-phenylethyl ester , methylpropyl)- , Uridine , 2′,3′-O-(phenylmethylene)- , 5′-(4-methylbenzenesulfo , Indolinol

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7

Mahmudova, F., A. Maksumova, N. Matkarimova, Sh Tadjieva, and I. Latipova. "Study of the reaction of olefins with acetic acid." E3S Web of Conferences 402 (2023): 14020. http://dx.doi.org/10.1051/e3sconf/202340214020.

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The purpose of this work is to study the esterification of liquid olefins with acetic acid in the presence of catalysts and to study the structure and properties of the synthesized saturated esters. 1-Hexene, 2-methyl-1-pentene, 2-ethyl-1-pentene, 3-methyl-1-pentene, and 3-methyl-2-pentene were used as liquid olefins and acid catalysts were used as catalysts for the esterification reaction: H2SO4 and HCl. The influence of various factors (the nature of the catalysts, the relative activity of olefins and temperature a) on the rate of the esterification reaction was studied. It has been shown th

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8

Nesvadba, Peter, Piotr Rzadek, and Günther Rist. "New Cyclodimerization Reaction of (3,5-Di-tert-butyl-4-oxocyclohexa-2,5-dienylidene)acetic Acid." Collection of Czechoslovak Chemical Communications 66, no. 8 (2001): 1250–56. http://dx.doi.org/10.1135/cccc20011250.

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(3,5-Di-tert-butyl-4-oxocyclohexa-2,5-dienylidene)acetic acid 1a underwent on heating a new cyclodimerization reaction affording a 1 : 1 mixture of the racemic cis- and trans-isomeric lactone-acids 2. The decisive structure elucidation of 2 was carried out after its mild esterification with diazomethane and separation of the racemic isomeric methyl esters 3a and 3b. The attempted esterification of 2 with methanol and sulfuric acid gave only the methyl diarylacetate 4. In contrast to 1a, which contains the carboxylic acid functionality no cyclodimerization was observed with the corresponding me

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9

Diniatik, Diniatik, Eka Retnowati та Asmiyenti D. Djalil. "19 Molecular Docking Analysis of Volatile Compounds from Fraction of Eichhornia crassipes Herbs Ethanol Extract As α-Glucosidase Inhibitor". Indonesian Journal of Pharmaceutical Science and Technology 10, № 1 (2023): 19. http://dx.doi.org/10.24198/ijpst.v10i1.32399.

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Diabetes mellitus is a degenerative disease characterized by an increase in blood sugar (hyperglycemia).Inhibiting it will prevent the uptake of glucose in the plasma. One of the plants that can be usedas antidiabetic is E. crassipes herbs. This research aims to know the interaction between volatilechemical compounds from ethyl acetate fraction and ethanol fraction of ethanol extract of E. crassipesherbs with the α-glucosidase enzyme. This study used ethanol extract of E. crassipes herbs with avariation of ethyl acetate fraction and ethanol fraction then analyzed the fraction using GC-MS (GasC

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10

Caravan, P., Suzanne M. Budge, and John M. Roscoe. "The reactions of O(3P) with some carboxylic acids and esters." Canadian Journal of Chemistry 74, no. 4 (1996): 516–23. http://dx.doi.org/10.1139/v96-056.

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The reactions of O(3P) with formic acid, acetic acid, methyl acetate, ethyl acetate, n-propyl acetate, and isopropyl acetate have been studied kinetically as a function of temperature. The rate constants were measured in a discharge-flow system under pseudo-first-order conditions with a large excess of the organic reagent. No reaction could be found between O(3P) and either formic acid or acetic acid in the temperature range 300–420 K. The acetate esters, on the other hand, reacted with O(3P) at readily measurable rates over the same temperature range. The temperature dependence of the rate co

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Book chapters on the topic "Adamantane-1-acetic acid methyl ester"

1

Winkelmann, J. "Diffusion of acetic acid methyl ester (1); air (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_642.

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2

Winkelmann, J. "Diffusion of acetic acid methyl ester (1); nitrogen (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_648.

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3

Winkelmann, J. "Diffusion of acetic acid methyl ester (1); carbon dioxide (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_646.

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4

Winkelmann, Jochen. "Diffusion coefficient of 1-methyl-2,4-dinitro-benzene into hexane and acetic acid ethyl ester solution." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_1197.

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5

Winkelmann, Jochen. "Diffusion coefficient of thiophosphoric acid O,O-diethyl O-[6-methyl-(1-methylethyl)-4-pyrimidinyl] ester into hexane and acetic acid ethyl ester solution." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_1313.

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6

Joule, J. A. "Method 1: From [(-Carboxyaryl)amino]acetic Acids and {[-(Alkoxycarbonyl)aryl]amino}acetic Acid Esters." In Science of Synthesis Knowledge Updates KU 2010/4. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-110-00313.

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7

Joule, J. A. "Method 1: From (-Nitroaryl)acetic Acids and Esters." In Science of Synthesis Knowledge Updates KU 2011/1. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-110-00277.

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