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Journal articles on the topic 'Dioxolane derivatives'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Dědek, Václav, and Ivan Hemer. "Photochemical chlorotrifluoroethylation of 1,2-, 1,3-, and 1,4-diols." Collection of Czechoslovak Chemical Communications 50, no. 12 (1985): 2743–52. http://dx.doi.org/10.1135/cccc19852743.

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The UV light-initiated reaction of chlorotrifluoroethylene with 1,2-ethanediol (I) proceeds only in the presence of acetone and affords 2-(2-chloro-1,1,2-trifluoroethyl)-2-methyl-1,3-dioxolane (VI). It has been proved that I is first photolyzed to acetaldehyde. Its acetalization in the reaction mixture gives 2-methyl-1,3-dioxolane (V) which then undergoes chlorotrifluoroethylation. The chlorotrifluoro derivative of 1,2-ethanediol XII was prepared by hydrolysis of 4-(2-chloro-1,1,2-trifluoroethyl)-2,2-dimethyl-1,3-dioxolane (XIII). 1,3-Propanediol (II) reacted to give 5-chloro-4,4,5-trifluoro-1

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2

Begum, Zahra, Momin Khan, Sher Wali Khan, et al. "Synthesis, Characterization, Antifungal and Antibacterial Activities of Novel Amide Derivatives of 1,3-Dioxolane." International Journal of Chemistry 11, no. 1 (2019): 71. http://dx.doi.org/10.5539/ijc.v11n1p71.

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L-Tartaric acid which is chiral compound and commercially available, was converted into 1,3-dioxolane. In the synthetic sequence, 1,3-dioxolane was first formed via protection and partial hydrolysis of L-tartaric acid. Treatment with altered substituted aromatic amines, 1,3-dioxolane gave the desired amides i.e. ethyl 2,2-dimethyl-5-(phenylcarbamoyl)-1,3-dioxolane-4-carboxylate 3a, 2-(4-(ethoxycarbonyl)-2,2-dimethyl-1,3-dioxolane-5-carboxamido)benzoic acid 3b, ethyl 5-(4-iodophenylcarbamoyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylate 3c, ethyl 5-(2-chlorophenylcarbamoyl)-2,2-di

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3

Raskil’dina, Gul’nara Z., Evgeniya A. Yakovenko, Luisa M. M. Mryasova, and Simon S. Zlotskii. "SYNTHESIS AND HERBICID ACTIVITY OF ARYLOXYACETIC ACIDS AND AMIDES OF ARYLOXY ACETIC ACIDS CONTAINING CYCLOACETAL FRAGMENT." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 62, no. 1 (2018): 91–97. http://dx.doi.org/10.6060/ivkkt.20196201.5753.

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The herbicidal activity of esters and amides based on commercially available phenoxy chlorides and 2,4-dichlorophenoxyacetic acids was studied. Esters of 2,2-methyl-4-hydroxymethyl-1,3-dioxolane, 5-ethyl-5-hydroxymethyl-1,3-dioxane and 1,3-dioxolan-4-ylmethanol and 1,3-dioxane-5 -ol (glycerin formulas), as well as amides containing gem-dichlorocyclopropane and 1,3-dioxolane fragments were obtained. The acid chlorides, 1,3-dioxacycloalkanes and secondary amines were prepared according to standard basic methods. Esters and amides were synthesized from these starting compounds in a short time and

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4

Vol’eva, V. B., I. S. Belostotskaya, N. L. Komissarova, A. V. Malkova, T. V. Pokholok, and E. Ya Davydov. "Antiradical activity of dioxolane derivatives." Russian Journal of Organic Chemistry 49, no. 3 (2013): 446–49. http://dx.doi.org/10.1134/s1070428013030226.

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5

Arnold, Donald R., and Laurie J. Lamont. "Photosensitized (electron transfer) carbon–carbon bond cleavage of radical cations: the 2-phenylethyl ether and acetal systems." Canadian Journal of Chemistry 67, no. 12 (1989): 2119–27. http://dx.doi.org/10.1139/v89-330.

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The scope of the photosensitized (electron transfer) carbon–carbon bond cleavage involving radical cations has been defined for 2-phenylethyl ethers and acetals. The thresholds for reactivity of the monophenylethyl and gem-diphenylethyl derivatives are compared. While the radical cation of methyl 2,2-diphenylethyl ether (7) cleaves to give ultimately diphenylmethane (2) and dimethoxymethane (8), the radical cation of methyl 2-phenylethyl ether (9) was stable under these conditions. In contrast to the lack of reactivity of the radical cation of 9, the radical cations of methyl 2-phenyl-2-propyl

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6

Tayebati, S. K., F. Amenta, A. Piergentili, M. Pigini, W. Quaglia, and M. Giannella. "Antimuscarinic activity of bicycle dioxolane derivatives." Life Sciences 60, no. 13-14 (1997): 1166. http://dx.doi.org/10.1016/s0024-3205(97)84305-6.

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7

Yuminov, V. S., S. V. Kartsov, V. L. Maksimov, and A. V. Fokin. "Perfluorinated dioxolanes 1. Synthesis of some derivatives of perfluoro-4-oxo-1,3-dioxolane." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 37, no. 2 (1988): 311–15. http://dx.doi.org/10.1007/bf00957432.

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8

Darko, Ampofo, Stephen Wallace, Olga Dmitrenko, et al. "Conformationally strained trans-cyclooctene with improved stability and excellent reactivity in tetrazine ligation." Chem. Sci. 5, no. 10 (2014): 3770–76. http://dx.doi.org/10.1039/c4sc01348d.

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9

Lv, Fan, Yang Yu, Erhong Hao та ін. "Highly regioselective α-formylation and α-acylation of BODIPY dyes via tandem cross-dehydrogenative coupling with in situ deprotection". Organic & Biomolecular Chemistry 17, № 20 (2019): 5121–28. http://dx.doi.org/10.1039/c9ob00927b.

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10

Borisova, Yulianna G., Rimma M. Sultanova, and Simon S. Zlotsky. "SYNTHESIS AND BIOLOGICAL ACTIVITY OF AMMONIUM SALTS CONTAINING CYCLOACETAL FRAGMENT." ChemChemTech 68, no. 2 (2024): 46–51. https://doi.org/10.6060/ivkkt.20256802.7127.

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Interaction of consecutive chain amines (pyridine, 2-methyl-pyridine, 4-vinyl-pyridine, 4-(1,3-dioxolan-2-yl)pyridine) with bromo derivatives (allyl bromide, benzyl and 2-β-bromoethyl-1 ) ,3-dioxolane), new quaternary ammonium salts were synthesized under thermal conditions containing allylic (1-allylpyridinium-, 1-allyl-4-vinylpyridinium- and 1-allyl-4-(1,3-dioxolan-2-yl) pyridinium bromides), benzyl (1-benzyl-4-vinylpyridinium-, 1-benzyl-4-(1,3-dioxolan-2-yl)pyridinium bromides) or 1,3-dioxolanoate (1-[2-(1 ,3-) dioxolan-2-yl)ethyl]pyridinium-, 1-[2-(1,3-dioxan-2-yl)ethyl]-2-methylpyridinium

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11

Chen, H., F. D. Boudinot, C. K. Chu, H. M. Mcclure, and R. F. Schinazi. "Pharmacokinetics of (-)-beta-D-2-aminopurine dioxolane and (-)-beta-D-2-amino-6-chloropurine dioxolane and their antiviral metabolite (-)-beta-D-dioxolane guanine in rhesus monkeys." Antimicrobial Agents and Chemotherapy 40, no. 10 (1996): 2332–36. http://dx.doi.org/10.1128/aac.40.10.2332.

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(-)-beta-D-2-Aminopurine dioxolane (APD) and (-)-beta-D-2-amino-6-chloropurine dioxolane (ACPD) are recently synthesized dioxolanylpurine nucleoside derivatives being developed as potential prodrugs for the antiviral nucleoside analog (-)-beta-D-dioxolane guanine (DXG). In vitro, APD and ACPD are converted to DXG by xanthine oxidase and adenosine deaminase, respectively. The purpose of this study was to evaluate the preclinical pharmacokinetics of APD and ACPD and their potential for generating sustained levels of the parent nucleoside, DXG, in rhesus monkeys following oral administration. Bot

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12

Rams-Baron, Marzena, Agnieszka Jędrzejowska, Mateusz Dulski, et al. "Unusual dielectric response of 4-methyl-1,3-dioxolane derivatives." Physical Chemistry Chemical Physics 20, no. 44 (2018): 28211–22. http://dx.doi.org/10.1039/c8cp05913f.

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In this paper, we applied broadband dielectric spectroscopy (BDS) to investigate the molecular dynamics of three 4-methyl-1,3-dioxolane derivatives (MD) whose chemical structures differ in the length of non-polar alkyl side chains.

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13

Nishikawa, Michihiro, Shota Sawamura, Aya Haraguchi, Jun Morikubo, Koichiro Takao, and Taro Tsubomura. "Highly emissive copper(i) complexes bearing diimine and bis(diphenylphosphinomethyl)-2,2-dimethyl-1,3-dioxolane." Dalton Transactions 44, no. 1 (2015): 411–18. http://dx.doi.org/10.1039/c4dt03176h.

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Highly emissive copper(i) complexes bearing 4,5-bis(diphenylphosphinomethyl)-2,2-dimethyl-1,3-dioxolane and 1,10-phenanthroline derivatives were newly synthesized. The quantum yields of the photoluminescence are up to 0.38.

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14

Clegg, W., B. T. Golding, B. J. King, and A. B. Maude. "Four Isomeric Dioxolane Derivatives of D-Camphorquinone." Acta Crystallographica Section C Crystal Structure Communications 51, no. 9 (1995): 1825–29. http://dx.doi.org/10.1107/s0108270195001788.

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15

Zhu, Huangtianzhi, Bingbing Shi, Lina Gao, et al. "Pillar[5]arene-based chiral 3D polymer network for heterogeneous asymmetric catalysis." Polymer Chemistry 8, no. 46 (2017): 7108–12. http://dx.doi.org/10.1039/c7py01669g.

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We report the preparation of a chiral 3D polymer network endowed with ability of heterogeneous asymmetric catalysis and good recyclability based on pillar[5]arene and (R,R)-tetraaryl-1,3-dioxolane-4,5-dimethanol derivatives.

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16

Spassova, Maria K., Antonín Holý, and Milena Masojídková. "Ribonucleosides of 3-amino- and 3,5-diaminopyrazole-4-carboxylic acid and their open-chain analogues: Synthesis and reactions." Collection of Czechoslovak Chemical Communications 51, no. 7 (1986): 1512–31. http://dx.doi.org/10.1135/cccc19861512.

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Bis(trimethylsilyl) derivative of ethyl 3-aminopyrazole-4-carboxylate (VI) and tris(trimethylsilyl) derivative of ethyl 3,5-diaminopyrazole-4-carboxylate (VII) on reaction with 2,3,5-tri-O-benzoyl-D-ribofuranolyl chloride and subsequent debenzoylation afforded the respective β-D-ribofuranosyl derivatives VIIIa and Xa. Their alkaline hydrolysis led to 1-(β-D-ribofuranosyl)-3-aminopyrazole-4-carboxylic acid (VIIIc) and 1-(β-D-ribofuranosyl)-3,5-diaminopyrazole-4-carboxylic acid (Xb). The esters VIIIa and Xa were not ammonolyzed under normal conditions. Contrary to nucleosidation of the silyl der

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17

Özkanlı, Fügen, Ahu Güney, Ünsal Çalış, and Tayfun Uzbay. "Synthesis and Anticonvulsant Activity of Some New Dioxolane Derivatives." Arzneimittelforschung 53, no. 11 (2011): 758–62. http://dx.doi.org/10.1055/s-0031-1299825.

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18

CLEGG, W., B. T. GOLDING, B. J. KING, and A. B. MAUDE. "ChemInform Abstract: Four Isomeric Dioxolane Derivatives of D-Camphorquinone." ChemInform 27, no. 4 (2010): no. http://dx.doi.org/10.1002/chin.199604038.

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19

LEE, S. J., J. K. PARK, and M. S. GONG. "ChemInform Abstract: Polymerization of 4-Methylene-1,3-dioxolane Derivatives." ChemInform 27, no. 8 (2010): no. http://dx.doi.org/10.1002/chin.199608133.

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20

Sakhabutdinova, G. N., G. Z. Raskil’dina, R. R. Chanyshev, and S. S. Zlotskii. "Synthesis of gem-Dichlorocyclopropane Derivatives Containing 1,3-Dioxolane Fragments." Reviews and Advances in Chemistry 12, no. 4 (2022): 255–58. http://dx.doi.org/10.1134/s263482762370006x.

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21

Azarifar, Davood, Maryam Golbaghi, Mahtab Pirveisian, and Zohreh Najminejad. "REGIOSELECTIVE AND FACILE OXIDATIVE THIOCYANATION OF ANILINES AND INDOLES WITH TRANS-3,5‐DIHYDROPEROXY‐3,5‐DIMETHYL‐1,2‐DIOXOLANE." JOURNAL OF ADVANCES IN CHEMISTRY 10, no. 8 (2014): 3088–96. http://dx.doi.org/10.24297/jac.v10i8.2247.

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Oxidative potential of trans‐3,5‐dihydroperoxy‐3,5‐dimethyl‐1,2‐dioxolane (DHPODMDO) has been explored in the facile thiocyanation of anilines and indoles through the efficient and in situ generation of SCN+ ion from sodium thiocyanate. The reactions proceed with regioselectivity under mild conditions at room temperature to afford the respective thiocyanate derivatives in excellent yields and low reaction times.

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22

Fangfang, Jian, Xiao Hailian, Xu Liangzhong, and Yu Guanping. "Synthesis and biological activities of some 2-(substituted-phenyl)-2-methyl-4-(1,2,4-triazole-1-yl)methane-1,3-dioxolane derivatives." Journal of Indian Chemical Society Vol. 81, Nov 2004 (2004): 974–77. https://doi.org/10.5281/zenodo.5833628.

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New Materials and Function Coordination Chemistry Laboratory, Qingdao University of Science and Technology, Qingdao Shandong 266042, China <em>E-mail</em>: ffj2003@163.169.net Fax: 86-532-4022989 <em>Manuscript received 15 September 2003, revised 5 May 2004, accepted 11 June 2004</em> The seven new triazole compounds containing 1,3-dioxolane were designed and synthesized. Their structures were identified by means of elemental analysis, IR, <sup>1</sup>H NMR and MS spectra. The results from the primary biological test show that all the compounds have some activities of fungicide and plant growt

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23

Efimtseva, Ekaterina V., Sergey N. Mikhailov, Sergey Meshkov, Teemu Hankamäki, Mikko Oivanen, and Harri Lönnberg. "Dioxolane nucleosides and their phosphonate derivatives: synthesis and hydrolytic stability." J. Chem. Soc., Perkin Trans. 1, no. 11 (1995): 1409–15. http://dx.doi.org/10.1039/p19950001409.

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24

Helesbeux, Jean-Jacques, Damien Peyronnet, Mehdi Labaïed, et al. "Synthesis and Antimalarial Activity of Some New 1,2-Dioxolane Derivatives." Journal of Enzyme Inhibition and Medicinal Chemistry 17, no. 6 (2002): 431–37. http://dx.doi.org/10.1080/1475636021000005677.

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25

Cassinelli, Anna, Piero Angeli, Mario Giannella та Fulvio Gualtieri. "β-Haloalkylamine derivatives with 1,3-oxathiolane or 1,3-dioxolane nuclei". European Journal of Medicinal Chemistry 22, № 1 (1987): 5–10. http://dx.doi.org/10.1016/0223-5234(87)90167-x.

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26

Corrado, Sandra, Claudia Sorbi, Annalisa Tait, et al. "1,4-Dioxolane-triazaspirodecanone derivatives as nociceptin/orphanin FQ receptor ligands." Medicinal Chemistry Research 23, no. 11 (2014): 4642–56. http://dx.doi.org/10.1007/s00044-014-1032-y.

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27

GAVRILOVA, S. P., T. G. SERKINA, and L. A. BADOVSKAYA. "ChemInform Abstract: Synthesis and Properties of Furan 1,3-Dioxolanes. Part 2. Synthesis of New Furan 1,3-Dioxolane Derivatives." ChemInform 25, no. 5 (2010): no. http://dx.doi.org/10.1002/chin.199405155.

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28

Möhrle, H., and M. Jeandrée. "1,3-Dioxolane von N-substituierten 4-Piperidonen als Dehydrierungssubstrat / 1,3-Dioxolanes of N-Substituted 4-Piperidones as Substrates for Dehydrogenations." Zeitschrift für Naturforschung B 52, no. 1 (1997): 72–78. http://dx.doi.org/10.1515/znb-1997-0115.

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The applicability of ketals was examined for masking the carbonyl group in N-tertiary 4-piperidones during the dehydrogenation using mercury-edta. Various 1,3-dioxolanes showed a different behaviour in dependence on the N-substituent. With simple aliphatic moieties mainly dehydrogenated but hydrolyzed products were received. These enaminones were also available from the dehydrogenations of the corresponding 4-piperidones. Similar applied to para-acyl-aromatic substituted derivatives but with less yields. Aromatic substituents bearing a neighbour group on ortho-position with participation gave

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29

Akash, Jain, Chaudhary Dushyant, and Chaudhary Jasmine. "Piperonal: The Journey so Far." Mini-Reviews in Medicinal Chemistry 20, no. 18 (2020): 1846–56. http://dx.doi.org/10.2174/1389557520666200711173149.

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Piperonal, an important aromatic aldehyde containing the benzene ring fused to 1, 3- dioxolane moiety, widely occurred in nature and known for its fragrance similar to vanillin and cherry. Alterations in its structural features led to the access of a wide range of piperonal derivatives viz. pyrazolines, chalcones, benzothiazepines, benzoxazoles, triazoles etc. having remarkable pharmacological properties like antimicrobial, anticancer, antidiabetic, antitubercular activities, etc. Therefore, the present study has been designed to highlight the progress made in the area of piperonal and its der

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30

Hrnčiar, Peter, Milan Hudeček, Gusein K. I. Magomedov та Štefan Toma. "Exploration of the new method for the synthesis of η6-arenetricarbonylchromium complexes. The scope and limitations". Collection of Czechoslovak Chemical Communications 56, № 7 (1991): 1477–81. http://dx.doi.org/10.1135/cccc19911477.

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A systematic investigation of the recently described method for the synthesis of η6-arenetricarbonylchromium complexes has been performed. The method gives the fair to excellent yields of complexes in a broad range of benzene derivatives and of some benzenoid arenes. Very low yields of products were obtained with benzene, 2-(2-chlorophenyl)-and 2-(3-fluorophenyl)-1,3-dioxolane. The method failed in the case of benzaldehyde, benzoic acid, benzyl chloride, nitrobenzene, thiophenol and chalcone.

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31

Ward, Dale E., та Yuanzhu Gai. "Synthesis of 10-methyl-Δ4-octalins by Diels–Alder reactions of 2H-thiopyran surrogates for 1-ethenyl-2-methylcyclohexene". Canadian Journal of Chemistry 75, № 6 (1997): 681–93. http://dx.doi.org/10.1139/v97-082.

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Diels–Alder reactions of 1-ethenyl-2-methylcyclohexene derivatives could be a versatile route to a variety of natural product skeletons that possess a 10-methyldecalin substructure with additional substitution at C-8 and C-9. These dienes are unreactive due (in part) to the presence of the vinyl methyl group, which destabilizes the necessary s-cis conformation. The use of 2H-thiopyran diene surrogates for 1-ethenyl-2-methylcyclohexene is investigated. The desired Diels–Alder adducts were not obtained by reaction of 6,7,8,8a-tetrahydro-5,5-dimethyl-3-tris(1-methylethyl)silyloxy-1H-2-benzothiopy

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32

Zykova, S. S., M. V. Shustov, and V. S. Talismanov. "Evaluation of the Antioxidant Properties and Cytotoxic Activity of 1,3-dioxolane Derivatives Imidazole." Drug development & registration 12, no. 4 (2023): 134–38. http://dx.doi.org/10.33380/2305-2066-2023-12-4(1)-1655.

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Introduction. Modern chemotherapy widely considers the role of antioxidant and pro-oxidant methods in the treatment of oncologic pathologies. The use of agents that cause an increase of ROS is a relevant way to destroy tumors. At the same time, there is evidence of the ability of some antioxidants to lead to the cancer cells apoptosis through the generation of free radical forms of oxygen due to disruption of cellular homeostasis. The combination of the «Ecolum» biosensor using technique, antiradical activity data, and information about the cytotoxicity of compounds used in the study allows us

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33

Sakakibara, Tohru, Aya Takaide, and Akinori Seta. "Photoaddition reactions of 3-nitro-2-enopyranoside derivatives in 1,3-dioxolane." Carbohydrate Research 226, no. 2 (1992): 271–78. http://dx.doi.org/10.1016/0008-6215(92)84075-4.

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34

Holý, Antonín, Ivan Rosenberg, and Hana Dvořáková. "Synthesis of (3-hydroxy-2-phosphonylmethoxypropyl) derivatives of heterocyclic bases." Collection of Czechoslovak Chemical Communications 54, no. 9 (1989): 2470–501. http://dx.doi.org/10.1135/cccc19892470.

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Analogs of the antiviral 9-(S)-(3-hydroxy-2-phosphonylmethoxypropyl)adenine (HPMPA, I), containing modified heterocyclic base, were prepared from racemic or (S)-N-(2,3-dihydroxypropyl) derivatives II. Compounds II are heated with chloromethylphosphonyl dichloride (XVII), the formed chloromethylphosphonylester chlorides of compounds II react with water to give a mixture of 2'- and 3'-chloromethylphosphonyl derivatives XVIII and XIX, respectively, which on isomerization by boiling with water in the arising acidic medium affords predominantly the 3'-isomer XIX. Treatment of this isomeric mixture

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35

Calmanti, Roberto, Emanuele Amadio, Alvise Perosa, and Maurizio Selva. "Reaction of Glycerol with Trimethyl Orthoformate: Towards the Synthesis of New Glycerol Derivatives." Catalysts 9, no. 6 (2019): 534. http://dx.doi.org/10.3390/catal9060534.

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The reactivity of glycerol with trimethyl orthoformate is here described with an emphasis on developing a reliable synthetic approach for glycerol valorization. The glycerol based orthoester 4-(dimethoxymethoxy)methyl)-2-methoxy-1,3-dioxolane (3) was synthesized, under catalytic as well as catalyst-free conditions, by taking advantage of the thermodynamically controlled equilibrium between intermediates. Both Brønsted and Lewis acid catalysts accelerated the attainment of such an equilibrium, particularly Brønsted acidic ionic liquids BSMImHSO4 and BSMImBr were the most effective compounds for

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36

Dvořáková, Hana, Antonín Holý, Ivan Votruba, and Milena Masojídková. "Synthesis and Biological Effects of Acyclic Analogs of Deazapurine Nucleosides." Collection of Czechoslovak Chemical Communications 58, no. 3 (1993): 629–48. http://dx.doi.org/10.1135/cccc19930629.

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Deaza analogs of three basic types of S-adenosyl-L-homocysteine hydrolase (SAHase) inhibitors, (S)-DHPA (I), eritadenine (II) and AHPA (III), were prepared. Alkylation of 3-deazaadenine (V), 3-deazapurine (VI), 1-deazaadenine (VII) and 4-amino-6-bromo-5-cyanopyrrolo[2,3-d]pyrimidine (XXII) with (R)-2,2-dimethyl-4-tosyloxymethyl-1,3-dioxolane (XIIIb), followed by acid hydrolysis, afforded the corresponding (S)-2,3-dihydroxypropyl derivatives XVIIa -XIXa and XXV. Reaction of V and VII with 2,3-O-cyclohexylidene-D-erythrono lactone (XXIX) and subsequent removal of the protecting groups in an acid

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37

Elagin, G. I., V. L. Mizyuk, L. O. Kobrin, and R. I. Vlyazlo. "Synthesis of tert-Alkylperoxy-substituted Derivatives of 2-Propanol, Dioxolane, and Thiirane." Russian Journal of Organic Chemistry 41, no. 11 (2005): 1666–70. http://dx.doi.org/10.1007/s11178-006-0016-x.

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38

EFIMTSEVA, E. V., S. N. MIKHAILOV, S. MESHKOV, T. HANKAMAEKI, M. OIVANEN, and H. LOENNBERG. "ChemInform Abstract: Dioxolane Nucleosides and Their Phosphonate Derivatives: Synthesis and Hydrolytic Stability." ChemInform 26, no. 38 (2010): no. http://dx.doi.org/10.1002/chin.199538272.

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39

Yang, Yu, František Mikeš, Liang Yang, Weihong Liu, Yasuhiro Koike, and Yoshiyuki Okamoto. "Novel amorphous perfluorocopolymeric system: Copolymers of perfluoro-2-methylene-1,3-dioxolane derivatives." Journal of Polymer Science Part A: Polymer Chemistry 44, no. 5 (2006): 1613–18. http://dx.doi.org/10.1002/pola.21278.

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40

Kim, Tae-Mi, Youhyuk Kim, and Myoung-Seon Gong. "Ring-opening polymerization of 4-methylene-1,3-dioxolane derivatives with tungsten hexachloride." Macromolecular Rapid Communications 15, no. 8 (1994): 639–45. http://dx.doi.org/10.1002/marc.1994.030150804.

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41

Wolak, M. A., J. Delcamp, C. A. Landis, P. A. Lane, J. Anthony, and Z. Kafafi. "High-Performance Organic Light-Emitting Diodes Based on Dioxolane-Substituted Pentacene Derivatives." Advanced Functional Materials 16, no. 15 (2006): 1943–49. http://dx.doi.org/10.1002/adfm.200500809.

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42

Jílek, Jiří, Miroslav Rajšner, Vladimír Valenta, et al. "Synthesis of piperidine derivatives as potential analgetic agents." Collection of Czechoslovak Chemical Communications 55, no. 7 (1990): 1828–53. http://dx.doi.org/10.1135/cccc19901828.

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Reaction of N-(1-(2-phenylethyl)-4-piperidinyl)propionanilide (I) with phosphorus pentasulfide gave the thioamide VI. Acylation of N-(1-(2-phenylethyl)-4-piperidinyl)aniline with 2-(methoxy)acetic and 2-(methylthio)acetic anhydrides afforded the amides II and III. Treatment of 4-anilino-1-benzylpiperidine-4-methanol with thionyl chloride gave the spirocyclic sulfurous acid ester amide XIV. Reduction of the hydrochloride of ethyl 3-(1-ethoxycarbonyl-4-phenylimino-3-piperidinyl)propionate (XXII) with sodium cyanoborohydride gave the perhydro-1,6-naphthyridine derivative XIX, a model compound in

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43

Zarzyka-Niemiec, Iwona. "Reactions of N,N′-bis(2-hydroxyethyl)oxalamide with Ethylene Carbonate and Use of the Obtained Products as Components of Polyurethanes Foams." International Journal of Polymer Science 2010 (2010): 1–9. http://dx.doi.org/10.1155/2010/689837.

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-bis(2-hydroxyethyl)oxalamide (BHEOA) was subject to hydroxyalkylation with ethylene carbonate (EC). By means of instrumental methods (IR, -NMR, MALDI ToF, GC, and GC-MS), an influence of the reaction conditions on structure and compositions of the obtained products was investigated. The hydroxyalkyl and hydroxyalkoxy derivatives of oxalamide (OA) were obtained by reaction of BHEOA with 2–10-molar excess of ethylene carbonate (EC, 1,3-dioxolane-2-one). The products have a good thermal stability and possess suitable physical properties as substrates for foamed polyurethanes. The obtained produc

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Kim, Seung Min, Sangkeun Son, Jong Won Kim, et al. "Penidioxolanes A and B, 1,3-Dioxolane Containing Azaphilone Derivatives from Marine-derivedPenicilliumsp. KCB12C078." Natural Product Sciences 21, no. 4 (2015): 231. http://dx.doi.org/10.20307/nps.2015.21.4.231.

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45

Jeong, In Howa, Sung Lan Jeon, and Bum Tae Kim. "Preparation of 4-trifluoroethylidene-1,3-dioxolane derivatives via new stable (trifluoromethyl)ethynylation reagent." Tetrahedron Letters 44, no. 38 (2003): 7213–16. http://dx.doi.org/10.1016/s0040-4039(03)01779-9.

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46

Shevchuk, A. S., V. A. Podgornova та B. F. Ustavshchikov. "ChemInform Abstract: Synthesis of 1,3-Dioxolane Derivatives from β-Chlorolactic Acid and Ketones." ChemInform 32, № 52 (2010): no. http://dx.doi.org/10.1002/chin.200152113.

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He, Jun-Yi, Fei-Xue Gao, and Rui-Mao Hua. "Heteropolyacid-catalyzed Reaction of Epoxides with Ketones: Efficient Synthesis of 1,3-Dioxolane Derivatives." Chinese Journal of Chemistry 23, no. 9 (2005): 1275–77. http://dx.doi.org/10.1002/cjoc.200591275.

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48

SAKAKIBARA, T., A. TAKAIDE, and A. SETA. "ChemInform Abstract: Photoaddition Reaction of 3-Nitro-2-enopyranoside Derivatives in 1,3- Dioxolane." ChemInform 23, no. 46 (2010): no. http://dx.doi.org/10.1002/chin.199246245.

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49

Borisova, Yu G., A. K. Bulgakov, N. S. Khusnutdinova, et al. "Synthesis and antimicrobial activity of functionally substituted 1,3-dioxacycloalkanes." Proceedings of Universities. Applied Chemistry and Biotechnology 14, no. 4 (2025): 453–61. https://doi.org/10.21285/achb.954.

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One of the directions in the development of organic chemistry is the synthesis of biologically active compounds, including those with bactericidal activity, based on available petrochemical raw materials. In order to expand the library of bioactive compounds containing a 1,3-dioxacyclane fragment, the synthesis of derivatives of 5-acyl-5-isopropyl-1,3-dioxane – 1-(5-isopropyl-1,3-dioxane-5-yl)ethanol and (5-isopropyl-1,3-dioxane-5-yl)ethyl phenyl carbamate was carried out. The effect of synthesized compounds containing a 1,3-dioxacyclane fragment on the growth of strains of gram-negative and g

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Holý, Antonín. "Syntheses of Enantiomeric N-(3-Hydroxy-2-phosphonomethoxypropyl) Derivatives of Purine and Pyrimidine Bases." Collection of Czechoslovak Chemical Communications 58, no. 3 (1993): 649–74. http://dx.doi.org/10.1135/cccc19930649.

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Methods of preparation of N-(3-hydroxy-2-phosphonomethoxypropyl) (HPMP) derivatives of (2S)- and (2R)-configuration (compounds I and XXVII, respectively) are described. The general method starts from the corresponding N-(2,3-dihydroxypropyl) derivatives which were converted either into the (R)-enantiomers XIII by reaction of the base with (R)-glycidol butyrate (XII) in the presence of cesium carbonate and subsequent methanolysis, or into the (S)-enantiomers XI by alkylation of the base with (R)-2,2-dimethyl-4-tosyloxymethyl-1,3-dioxolane (V) in the presence of the same reagent. The amino group

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