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Relevant bibliographies by topics / Maleic Anhydride Adduct

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Academic literature on the topic 'Maleic Anhydride Adduct'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Maleic Anhydride Adduct"

1

Roussel, C., V. Marchetti, A. Lemor, E. Wozniak, B. Loubinoux, and P. Gérardin. "Chemical Modification of Wood by Polyglycerol/Maleic Anhydride Treatment." Holzforschung 55, no. 1 (2001): 57–62. http://dx.doi.org/10.1515/hf.2001.009.

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Summary Polyglycerol (PG), an agricultural by-product of diester industry, was reacted with maleic anhydride (MA) to give heat curable compounds which are useful for impregnating wood to improve biological resistance, dimensional stability and strength. The relationships between reaction conditions of polyglycerol/maleic anhydride (PG/MA) adduct treatment and performance of treated solid wood were investigated. Conditions recommended for producing PG/MA treated wood durable for a long time are vacuum/pressure impregnation of aqueous solutions of PG/MA adduct (30%) in the presence of 2-butanone

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2

Pearson, JR, and QN Porter. "Vinylindenes and Some Heteroanalogs in the Diels-Alder Reaction. X. Dibenzofurans From 3-Vinylbenzofurans." Australian Journal of Chemistry 44, no. 8 (1991): 1085. http://dx.doi.org/10.1071/ch9911085.

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3-Vinylbenzofuran, 3-isopropenylbenzofuran and 2-methyl-3-vinylbenzofuran give normal [4π+2π] adducts with ethenetetracarbonitrile, accompanied, in the case of the last named diene, by the isomeric cyclobutane. Normal adducts also result from these dienes and 4-phenyl-1,2,4-triazoline-3,5-dione, and from 3-vinylbenzofuran and both maleic anhydride and N- phenylmaleimide. 3-Vinylbenzofuran gives the rearranged adduct dimethyl 1,2-dihydrodibenzofuran-3,4-dicarboxylate with dimethyl acetylenedicarboxylate.

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3

Nie, Yuan Mei, Kun Gang Chai, Zhan Wan Shi та Xing Dong Yao. "Investigation on the Synthesis of α-Terpinene and Maleic Anhydride Adduct Catalyzed by Heteropolyacid". Advanced Materials Research 361-363 (жовтень 2011): 1063–65. http://dx.doi.org/10.4028/www.scientific.net/amr.361-363.1063.

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α-pinene was isomerized in the presence of phosphomolybdic acid. One of the products, α-terpinene, can react with maleic anhydride to form α-terpinene and maleic anhydride adduct (TMA). The optimum conditions for the synthesis of TMA have been investigated. The yield of 83% can be attained with the heterogeneous catalyst phosphomolybdic acid on active carbon (PMA/C), and can maintain ~67% after the catalyst was used for 5 times.

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4

Chakkaravarthy, Jayaraman, Inbasekaran Muthuvel, and Ganesamoorthy Thirunarayanan. "Spectral investigations of some piperidin-4-one molecular addition compounds." Ovidius University Annals of Chemistry 31, no. 1 (2020): 18–26. http://dx.doi.org/10.2478/auoc-2020-0005.

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AbstractIn the present study, some 2- and 3-substituted piperidin-4-ones (A1-A3) were chosen as proton acceptor and maleic anhydride was chosen as proton donor. Piperidin-4-ones (A1, A2 ---amp--- A3) were mixed with maleic anhydride in ether medium and the corresponding molecular adduct products (B1, B2 ---amp--- B3) thus obtained were collected and purified. The 1H and 13C NMR spectra were recorded for piperidine-4-one and their addition compounds. The 1H and 13C NMR chemical shifts of products (B1, B2 ---amp--- B3) are analyzed and compared with those of the corresponding piperidine-4-ones (

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5

ASHOK, KUMAR SINGH, та K. SRIVASTAVA S. "Stereochemistry of the Oxime of N-Hydroxyimide of β-Naphthol-Maleic Anhydride Adduct". Journal of Indian Chemical Society Vol. 65, Oct 1988 (1988): 732–33. https://doi.org/10.5281/zenodo.6106160.

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Department of Chemistry, University of Roorkee, Roorkee-247 667 <em>Manuscript received 8 February 1988, revised 27 May 1988, accepted 18 July 1988</em> Stereochemistry of the Oxime of <em>N</em>-Hydroxyimide of <em>β</em>-Naphthol-Maleic Anhydride Adduct.

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6

Chen, Xiaoyu, Andrew Thomas Holm, and Philip Wai Hong Chan. "Gold Catalysed 1,4-Enyne Acetate Strategy for the Synthesis of 1H-Indenes and Partially Hydrogenated Methanonaphtho[1,2-c]furan-1,3(4H)-diones." Australian Journal of Chemistry 73, no. 12 (2020): 1165. http://dx.doi.org/10.1071/ch20175.

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A synthetic method to prepare 1H-indenes and partially hydrogenated methanonaphtho[1,2-c]furan-1,3(4H)-diones from gold(i)-catalysed 1,4-enyne acetate cycloisomerisation and oxidation or Diels–Alder reaction with maleic anhydride is described. The proposed mechanism involves Rautenstrauch rearrangement of the 1,4-enyne motif to give an insitu formed 1,3-cyclopentadiene intermediate. This is followed by 6-endo-dig cyclisation of the cyclic adduct and oxidation to give the aromatic carbocycle or Diels–Alder reaction with maleic anhydride to afford the bridged furan product.

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7

Brown, Richard T., Simon B. Jameson, Dehimi Ouali, and Peter I. Tattersall. "Synthesis of Chiral Polyfunctionalised Cyclopentanes from the Diels–Alder Adduct of Furan and Maleic Anhydride." Journal of Chemical Research 2000, no. 4 (2000): 176–78. http://dx.doi.org/10.3184/030823400103166850.

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Chiral polyfunctionalised cyclopentanes have been readily obtained in ~65% enantiomeric excess via a stereo-specific Wagner–Meerwein rearrangement induced by bromination of derivatives of the exo-cis Diels–Alder adduct of furan and maleic anhydride, combined with desymmetrisation of a meso intermediate by pig liver esterase.

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8

Abate, Diane Wolfer, and Malcolm P. Stevens. "Unsaturated polyester containing myrcene–maleic anhydride Diels–Alder adduct." Journal of Applied Polymer Science 46, no. 3 (1992): 389–91. http://dx.doi.org/10.1002/app.1992.070460303.

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9

Akai, Shuji, Shuhei Hori, Sho Ishida, et al. "Synthetic Studies on the Viridin Skeleton through Regio- and Stereoselective Functionalization of the AE-Ring Moiety." Synlett 32, no. 12 (2021): 1187–91. http://dx.doi.org/10.1055/a-1527-3781.

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Abstract4,5,6,7-Tetrahydroisobenzofurans, corresponding to the AC(D)E ring structure of viridin and equipped with required substituents on the A-ring, were synthesized with high regio- and stereoselectivities via the Diels–Alder adduct of a furan derivative and maleic anhydride. The key steps of this work include the regioselective opening of a tetrahydrofuran ring, a stereoselective epoxidation, and an AlMe3-mediated regioselective epoxide opening followed by stereoselective C-methylation.

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10

Tolstikov, Aleksander G., Olga V. Tolstikova, Tatiana B. Khlebnikova, et al. "Chiral organophosphorus ligands derived from the levopimaric acid-maleic anhydride adduct." Mendeleev Communications 6, no. 6 (1996): 215–17. http://dx.doi.org/10.1070/mc1996v006n06abeh000730.

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Conference papers on the topic "Maleic Anhydride Adduct"

1

Kornilov, Dmitry, Yury Zimin, Irina Alekhina, Aliya Kornilova, and Akhat Mustafin. "Synthesis and x-ray diffraction study of the adduct of the Diels-Alder reaction between thiophene and maleic anhydride." In Third International Scientific and Practical Symposium on Materials Science and Technology (MST-III 2023), edited by Ramazon Abdullozoda and Shahriyor Sadullozoda. SPIE, 2024. http://dx.doi.org/10.1117/12.3017743.

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