Relevant bibliographies by topics / Dioxolane derivatives

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Dioxolane derivatives'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Dioxolane derivatives"

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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Dissertations / Theses on the topic "Dioxolane derivatives"

1

Gerard, Eric-Jack. "Synthese, caracterisation et comportement de polyurethannes hydrophiles : etude du mecanisme de la polycondensation reticulante." Université Louis Pasteur (Strasbourg) (1971-2008), 1988. http://www.theses.fr/1988STR13192.

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Synthese d'hygrogels, constitues de chaines elastiques de polydioxolanne. Les reticulats sont synthetises en milieu organique par couplages multiples des extremites hydroxylees, du polydioxolanne precurseur avec un compose isocyanate plurifonctionnel. Apres reaction, un echange progressif du solvant organique par l'eau permet d'obtenir les hydrogels
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Book chapters on the topic "Dioxolane derivatives"

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Ihmels, H. "Cyclization of 2-(1,3-Dioxolan-2-yl)-1-(2-oxopropyl)pyridinium Derivatives." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-01556.

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Conference papers on the topic "Dioxolane derivatives"

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Savchenko, R. G., V. N. Odinokov, and L. V. Parfenova. "Diastereoselective synthesis of novel 20-hydroxyecdysone dioxolane derivatives." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0069194.

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Journal articles
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