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Gotowe bibliografie tematyczne / (±)-Camphor-10-sulfonic acid

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Artykuły w czasopismach

Gotowa bibliografia na temat „(±)-Camphor-10-sulfonic acid”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "(±)-Camphor-10-sulfonic acid"

1

Sokolova, A. S., O. I. Yarovaya, L. V. Kuzminykh, et al. "Synthesis and Properties of (+)-Ketopinic and (–)-Camphanic Acids Esters Bearing a Nitrogen-Containing Heterocycle." Russian Journal of General Chemistry 93, no. 12 (2023): 3062–73. http://dx.doi.org/10.1134/s1070363223120058.

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Abstract A three-stage method was proposed for the synthesis of (1S)-(+)-camphor-10-sulfonic acid, (+)-ketopinic and (–)-camphanic acids esters containing a saturated nitrogen-containing heterocycle. It was found that (1S)-(+)-camphor-10-sulfonic acid esters undergo destruction with elimination of the sulfonic acid group in substitution reactions involving nitrogen-containing heterocycles. Esters of (+)-ketopinic and (–)-camphanic acids were formed during the proposed synthetic route, but undergo transesterification under column chromatography conditions. Quantum chemical calculations showed t

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2

Sokolova, A. S., O. I. Yarovaya, L. V. Kuzminykh, et al. "Synthesis and properties of (+)-ketopinic and (-)-camphanic acids esters bearing a nitrogen-containing heterocycle." Журнал общей химии 93, no. 12 (2023): 1854–66. http://dx.doi.org/10.31857/s0044460x23120053.

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A three-stage method was proposed for the synthesis of (1 S )-(+)-camphor-10-sulfonic acid, (+)-ketopinic and (-)-camphanic acids esters containing a saturated nitrogen-containing heterocycle. It was found that (1 S )-(+)camphor-10-sulfonic acid esters undergo destruction with elimination of the sulfonic acid group in substitution reactions involving nitrogen-containing heterocycles. Esters of (+)-ketopinic and (-)-camphanic acids were formed during the proposed synthetic route, but undergo transesterification under column chromatography conditions. Quantum chemical calculations showed that th

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3

Brahmachari, Goutam, Khondekar Nurjamal, Indrajit Karmakar, and Mullicka Mandal. "Camphor-10-Sulfonic Acid (CSA): A Water Compatible Organocatalyst in Organic Transformations." Current Organocatalysis 5, no. 3 (2019): 165–81. http://dx.doi.org/10.2174/2213337205666181112110524.

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4

Anjaneyulu, Bendi, Sangeeta, and Naina Saini. "A Study on Camphor Derivatives and Its Applications: A Review." Current Organic Chemistry 25, no. 12 (2021): 1404–28. http://dx.doi.org/10.2174/1385272825666210608115750.

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Natural compounds are the prominent sources for the synthesis of abundant biologically active substances in medicinal chemistry. Camphor exists in two enantiomeric forms i.e., R and S, or both, which are readily obtainable. Camphor is a small molecule with chirality property that binds to some active site, together with its low cost and convenience to transform into synthetically useful derivatives and one of the most important monoterpenoids widely spread in plants and has been used as starting material for the various camphor based derivatives which exhibit several biological activities incl

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5

Pelit, Emel, and Zuhal Turgut. "(+)-CSA Catalyzed Multicomponent Synthesis of 1-[(1,3-Thiazol-2-ylamino)methyl]-2-naphthols and Their Ring-Closure Reaction under Ultrasonic Irradiation." Journal of Chemistry 2016 (2016): 1–9. http://dx.doi.org/10.1155/2016/9315614.

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New 1-[(1,3-thiazol-2-ylamino)methyl]-2-naphthols were obtained by condensation of 2-aminothiazole, aromatic aldehydes, and 2-naphthol in the presence of (+)-camphor-10-sulfonic acid ((+)-CSA) as an effective catalyst under ultrasound-promoted solvent-free conditions. The 1-[(1,3-thiazol-2-ylamino)methyl]-2-naphthol derivatives were converted in ring-closure reaction with formaldehyde to the corresponding naphthoxazine derivatives.

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6

Garai, Ashesh, and Arun K. Nandi. "Rheology of (±)-camphor-10-sulfonic acid doped polyaniline-m-cresol conducting gel nanocomposites." Journal of Polymer Science Part B: Polymer Physics 46, no. 1 (2008): 28–40. http://dx.doi.org/10.1002/polb.21339.

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7

Pelit, Emel. "Synthesis of Isoxazolopyridines and Spirooxindoles under Ultrasonic Irradiation and Evaluation of Their Antioxidant Activity." Journal of Chemistry 2017 (2017): 1–9. http://dx.doi.org/10.1155/2017/9161505.

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New polycyclic-fused isoxazolo[4,5-e]pyridines and spirooxindoles were obtained via multicomponent reaction of 5-amino-3-methylisoxazole, indan-1,3-dione, and aromatic aldehydes and reaction of 5-amino-3-methylisoxazole, isatin, and β-diketones in the presence of (±)-camphor-10-sulfonic acid as an effective and nontoxic organocatalyst under ultrasound-promoted conditions. The antioxidant activity of the novel synthesized compounds was studied.

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8

Manna, Swarup, and Arun K. Nandi. "Supramolecular Organization of ±Camphor-10-sulfonic Acid andN,N-Dimethyl Formamide into Giant Spherulites." Journal of Physical Chemistry B 108, no. 22 (2004): 6932–34. http://dx.doi.org/10.1021/jp048824g.

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9

Kas’yan, L. I., V. A. Pal’chikov, A. V. Turov, S. A. Prid’ma, and A. V. Tokar’. "Cage-like amines in the synthesis and oxidation of camphor-10-sulfonic acid amides." Russian Journal of Organic Chemistry 45, no. 7 (2009): 1007–17. http://dx.doi.org/10.1134/s1070428009070057.

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10

Cai, Liying, Tingping Xie, Suying Zhao, Huidong Zheng, and Dan Wu. "Measurement and correlation of solubility of d-camphor-10-sulfonic acid in pure solvents." Fluid Phase Equilibria 398 (July 2015): 46–50. http://dx.doi.org/10.1016/j.fluid.2015.04.014.

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