Relevant bibliographies by topics / Diethyl acetals

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

Academic literature on the topic 'Diethyl acetals'

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

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Journal articles on the topic "Diethyl acetals"

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Ferro, V., M. Mocerino, RV Stick, and DMG Tilbrook. "An Improvement in the Preparation of Some Carbohydrate Benzylidene Acetals." Australian Journal of Chemistry 41, no. 5 (1988): 813. http://dx.doi.org/10.1071/ch9880813.

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Carbohydrate benzylidene and p- methoxybenzylidene acetals are easily prepared by treatment of various sugar derivatives with either benzaldehyde diethyl acetal or p- methoxybenzaldehyde diethyl acetal , respectively, in refluxing chloroform containing camphorsulfonic acid.
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2

Pestov, Alexander, Yuliya Privar, Arseny Slobodyuk, Andrey Boroda, and Svetlana Bratskaya. "Chitosan Cross-Linking with Acetaldehyde Acetals." Biomimetics 7, no. 1 (2022): 10. http://dx.doi.org/10.3390/biomimetics7010010.

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Here we demonstrate the possibility of using acyclic diethylacetal of acetaldehyde (ADA) with low cytotoxicity for the fabrication of hydrogels via Schiff bases formation between chitosan and acetaldehyde generated in situ from acetals in chitosan acetate solution. This approach is more convenient than a direct reaction between chitosan and acetaldehyde due to the better commercial availability and higher boiling point of the acetals. Rheological data confirmed the formation of intermolecular bonds in chitosan solution after the addition of acetaldehyde diethyl acetal at an equimolar NH2: acet
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Xu, Tongyu, Zhengkun Yu, and Liandi Wang. "Iron-Promoted Cyclization/Halogenation of Alkynyl Diethyl Acetals." Organic Letters 11, no. 10 (2009): 2113–16. http://dx.doi.org/10.1021/ol9005689.

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Grindley, T. Bruce, Srihari Kusuma, and T. Stanley Cameron. "Kinetic benzylidenation. Part I. The selective formation of five-membered ring benzylidene acetals from aldose diethyl dithioacetals." Canadian Journal of Chemistry 64, no. 12 (1986): 2388–96. http://dx.doi.org/10.1139/v86-395.

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Reaction of D-arabinose diethyl dithioacetal with one equivalent of benzaldehyde dimethyl acetal in the presence of p-toluenesulfonic acid at −40 °C gave a mixture of the two epimers of 5-O-methoxyphenylmethyl-D-arabinose diethyl dithioacetal initially. After 14 h at −20 °C, the major products were R- and S-4,5-O-benzylidene-D-arabinose diethyl dithioacetal. The structure of the S isomer was determined by X-ray crystallography. The crystal was orthorhombic, with space group P212121, cell dimensions a = 5.179(4), b = 12.469(3), c = 27.150(4) Å, and Z = 4. The crystal structure was solved using
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Jin-Chang, Ding, Xu Rong, Liu Miao-Chang, Chen Xi-An, and Wu Hua-Yue. "Gallium triiodide as a highly efficient and mild catalyst for the diethyl acetalization of carbonyl compounds." Journal of Indian Chemical Society Vol. 85, May 2008 (2008): 566–68. https://doi.org/10.5281/zenodo.5816547.

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Wenzhou Vocational and Technical College, Wenzhou, Zhejiang 325035, P. R. China E-mail : djc@wzvtc.cn Fax : 86-577-86680188 College of Chemistry and Materials Science, Wenzhou University, Wenzhou, Zhejiang 325027, P.R. China <em>E-mail :</em> hywu3@163.com&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; Fax : 86-577-88368280 <em>Manuscript received 15 February 2007. revised 28 December 2007, accepted 6 March 2008</em> Diethyl acetals were obtained from carbonyl compounds in good to excellent yields under mild reaction conditions in the presence of triethyl orthoformate and
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Gao, Fuye, and D. Jean Burnell. "Reactions of 1,2-Bis(trimethylsilyloxy)cycloalkenes with the Diethyl Acetals of Aldehydes." Journal of Organic Chemistry 71, no. 1 (2006): 356–59. http://dx.doi.org/10.1021/jo051683+.

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Boyer, Bernard, Rafik Kalfat, Gerard Lamaty, and Jean Pierre Roque. "Reactivity in reverse micelles: acid-catalysed hydrolysis of para-substituted benzaldehyde diethyl acetals." Journal of the Chemical Society, Perkin Transactions 2, no. 7 (1988): 1325. http://dx.doi.org/10.1039/p29880001325.

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Fisyuk, A. S., and A. Yu Mukanov. "Synthesis of 3-isothiocyanatopropion-and-butyraldehyde diethyl acetals and their reactions with n-nucleophiles." Russian Journal of Organic Chemistry 42, no. 9 (2006): 1269–74. http://dx.doi.org/10.1134/s107042800609003x.

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Matsumoto, Toshihiko. "Simple One–Pot Synthesis of Hexakis(2-alkoxy-1,5-phenyleneimine) Macrocycles by Precipitation–Driven Cyclization." Macromol 4, no. 1 (2024): 1–22. http://dx.doi.org/10.3390/macromol4010001.

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Hexakis(2-alkoxy-1,5-phenyleneimine) macrocycles were synthesized using a simple one-pot procedure through precipitation-driven cyclization. The acetal-protected AB–type monomers, 2-alkoxy-5-aminobenzaldehyde diethyl acetals, underwent polycondensation in water or acid-containing tetrahydrofuran. The precipitation–driven cyclization, based on imine dynamic covalent chemistry and π–stacked columnar aggregation, played a decisive role in the one–pot synthesis. The progress of the reaction was analyzed using MALDI–TOF mass spectrometry. The macrocycles with alkoxy chains were soluble in specific
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Thibaud, Fannie, Svitlana Shinkaruk, and Philippe Darriet. "Quantitation, Organoleptic Contribution, and Potential Origin of Diethyl Acetals Formed from Various Aldehydes in Cognac." Journal of Agricultural and Food Chemistry 67, no. 9 (2019): 2617–25. http://dx.doi.org/10.1021/acs.jafc.9b01084.

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Dissertations / Theses on the topic "Diethyl acetals"

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Bao, Congyu. "Cellulose acetate / plasticizer systems : structure, morphology and dynamics." Thesis, Lyon 1, 2015. http://www.theses.fr/2015LYO10049/document.

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Les polysaccharides sont l'une des principales options à retenir pour progresser dans l'utilisation ou la conception de polymères renouvelables. Depuis les années cinquante, le développement industriel de ce type de polymères s'était considérablement réduit du fait de l'avènement des polymères synthétiques. Cependant, cet intérêt a cru considérablement ces dernières années en raison de la sensibilisation du public sur la limite des ressources fossiles. Ces biopolymères sont donc devenus un sujet d'importance, tant sur le plan industriel que sur celui de la recherche fondamentale. Toutefois, le
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Guo, Ruichao. "Nicholas reactions of 2,5-heptadiyne diether and ether/acetate tetracobalt complexes and synthesis of cyclophanediynes." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0031/MQ62217.pdf.

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Best, Emmanuelle. "Influence des polyoxyéthylènes-glycols et du phtalate de diéthyle sur la cinétique de dissolution de comprimés d'aminophylline enrobés par l'acétate de cellulose." Paris 5, 1993. http://www.theses.fr/1993PA05P227.

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Andriamadio, Pascal. "Amino-2 thiophènes et dérivés : Constantes d'acidité et mesures de rotations empêchées en milieux non aqueux." Nancy 1, 1986. http://www.theses.fr/1986NAN10957.

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Les amino-2 thiophènes diversement substitués en position 5 sont insolubles dans l'eau et la première partie de ce travail a consisté à rechercher des solvants aprotiques suffisamment dissociants pour permettre la mesure du pH au moyen d'indicateurs colorés. Des relations de BRONSTED satisfaisantes ont été obtenues respectivement dans l'acétonitrile et dans le DMSO. Dans la deuxième partie, l'étude par RMN des autres dérivés R5 = H, CI, COCH3, CHO et NO2 a permis de montrer que le rapport de population entre les deux isomères X et Y s'inverse par passage de NO2 à H (PX/PY = 0. 074 et 9,65 dans
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Lin, Mei-Jyun, and 林美君. "Density and viscosity measurements of binary mixtures of diethyl oxalate with ethanol, toluene, tetrahydrofuran, N,N-dimethylformamide and ethyl acetate." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/be79c8.

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碩士<br>國立臺北科技大學<br>化學工程研究所<br>102<br>In this study, density and viscosity data of five binary mixtures consisted of diethyl oxalate and organic solvent are reported. Five solvents including ethanol, toluene, tetrahydrofuran, N,N-dimethylformamide and ethyl acetate are considered in our measurement. Density and viscosity data of these five binary mixtures are measured at 303.15, 313.15 and 323.15 K and mole fraction of diethyl oxalate at 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8 and 0.9. In addition, excess molar volume and deviation of viscosity are also calculated from our experimental data. Acco
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Book chapters on the topic "Diethyl acetals"

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Bährle-Rapp, Marina. "Diethyl Acetyl Aspartate." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_2921.

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Holze, Rudolf. "Ionic conductivities of acetaldehyde diethyl acetal." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_239.

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Wohlfarth, Ch. "Second virial coefficient of poly(diethyl maleate-co-vinyl acetate)." In Polymer Solutions. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02890-8_465.

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Wohlfarth, Ch. "Refractive index of the mixture (1) vinyl acetate; (2) diethyl carbonate." In Refractive Indices of Pure Liquids and Binary Liquid Mixtures (Supplement to III/38). Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75291-2_847.

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Leung, M. k., and T. Y. Luh. "Catalyzed by Boron Trifluoride–Diethyl Ether Complex." In Acetals: O/N, S/S, S/N, and N/N and Higher Heteroatom Analogues. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-030-00195.

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Kibayashi, C., and N. Yamazaki. "Rhodium-Catalyzed Reaction with Diethyl(methyl)silane and Carbon Monoxide." In Acetals: O/N, S/S, S/N, and N/N and Higher Heteroatom Analogues. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-030-00512.

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Kibayashi, C., and N. Yamazaki. "Reductive Cleavage with Sodium Borohydride–Boron Trifluoride–Diethyl Ether Complex." In Acetals: O/N, S/S, S/N, and N/N and Higher Heteroatom Analogues. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-030-00047.

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Scarso, A., and G. Strukul. "Reaction of Acetals with Hydrogen Peroxide Mediated by Boron Trifluoride–Diethyl Ether Complex." In Peroxides, Inorganic Esters (RO-X, X=Hal, S, Se, Te, N). Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-038-00063.

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Nakata, M. "Using Hydrogen Chloride, Zinc(II) Chloride, or Boron Trifluoride–Diethyl Ether Complex." In Acetals: O/N, S/S, S/N, and N/N and Higher Heteroatom Analogues. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-030-00275.

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Nakata, M. "Using Hydrogen Chloride, 4-Toluenesulfonic Acid, or Boron Trifluoride–Diethyl Ether Complex." In Acetals: O/N, S/S, S/N, and N/N and Higher Heteroatom Analogues. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-030-00328.

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Conference papers on the topic "Diethyl acetals"

1

Luo, Cai-Wu, An Li, Shan Liang, Bo Lei, Zheng-Hao Wang, and Zi-Sheng Chao. "Study on screening catalysts for the synthesis of acrolein diethyl acetal/ammonia toward pyridine and 3-picoline." In THE 3RD INTERNATIONAL CONFERENCE ON MECHANICS, MATERIALS AND STRUCTURAL ENGINEERING 2018 (ICMMSE2018). Author(s), 2018. http://dx.doi.org/10.1063/1.5047112.

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