Relevant bibliographies by topics / Polydepsipeptides

Academic literature on the topic 'Polydepsipeptides'

Author: Grafiati
Published: 4 May 2024

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Journal articles on the topic "Polydepsipeptides"

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Feng, Yakai, and Jintang Guo. "Biodegradable Polydepsipeptides." International Journal of Molecular Sciences 10, no. 2 (February 13, 2009): 589–615. http://dx.doi.org/10.3390/ijms10020589.

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MAMMI, STEFANO, and MURRAY GOODMAN. "Polydepsipeptides. 13." International Journal of Peptide and Protein Research 28, no. 1 (January 12, 2009): 29–44. http://dx.doi.org/10.1111/j.1399-3011.1986.tb03227.x.

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Dijkstra, Pieter J., and Jan Feijen. "Synthetic pathways to polydepsipeptides." Macromolecular Symposia 153, no. 1 (March 2000): 67–76. http://dx.doi.org/10.1002/1521-3900(200003)153:1<67::aid-masy67>3.0.co;2-f.

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Becktel, W. J., G. Wouters, D. M. Simmons, and Murray Goodman. "Polydepsipeptides. 11. Conformational analysis of polydepsipeptides containing methyl, isopropyl, and isobutyl side chains." Macromolecules 18, no. 4 (July 1985): 630–34. http://dx.doi.org/10.1021/ma00146a009.

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Dijkstra, Pieter J., and Jan Feijen. "ChemInform Abstract: Synthetic Pathways to Polydepsipeptides." ChemInform 31, no. 47 (November 21, 2000): no. http://dx.doi.org/10.1002/chin.200047264.

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Mammi, Stefano, and Murray Goodman. "Polydepsipeptides. A systematic investigation of guest-host effects." Journal of Peptide Science 11, no. 5 (2005): 273–77. http://dx.doi.org/10.1002/psc.665.

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Ohya, Yuichi, Hidetoshi Yamamoto, Koji Nagahama, and Tatsuro Ouchi. "Effects of polydepsipeptide side-chain groups on the temperature sensitivity of triblock copolymers composed of polydepsipeptides and poly(ethylene glycol)." Journal of Polymer Science Part A: Polymer Chemistry 47, no. 15 (June 12, 2009): 3892–903. http://dx.doi.org/10.1002/pola.23456.

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Yoshida, Masaru, Masaharu Asano, Minoru Kumakura, Ryoichi Katakai, Tooru Mashimo, Hisako Yuasa, Kyoichi Imai, and Hidetoshi Yamanaka. "Sequential polydepsipeptides as biodegradable carriers for drug delivery systems." Journal of Biomedical Materials Research 24, no. 9 (September 1990): 1173–84. http://dx.doi.org/10.1002/jbm.820240904.

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Ouchi, Tasuro, Tatsuya Nozaki, Yoshifumi Okamoto, Masahiro Shiratani, and Yuichi Ohya. "Synthesis and enzymatic hydrolysis of polydepsipeptides with functionalized pendant groups." Macromolecular Chemistry and Physics 197, no. 6 (June 1996): 1823–33. http://dx.doi.org/10.1002/macp.1996.021970604.

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Yoshida, Masaru, Masaharu Asano, Minoru Kumakura, Ryoichi Katakai, Tooru Mashimo, Hisako Yuasa, and Hidetoshi Yamanaka. "Sequential polydepsipeptides containing tripeptide sequences and α-hydroxy acids as biodegradable carriers." European Polymer Journal 27, no. 3 (January 1991): 325–29. http://dx.doi.org/10.1016/0014-3057(91)90113-3.

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Dissertations / Theses on the topic "Polydepsipeptides"

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Burton, Tobias. "Synthèse de morpholine-2,5-diones et de (co)polydepsipeptides pour la valorisation d'acides aminés." Electronic Thesis or Diss., Montpellier, 2020. http://www.theses.fr/2020MONTS110.

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Au cours de ce travail, l’élaboration, la polymérisation et la copolymérisation organocatalysée des morpholine-2,5-diones, des monomères cycliques produits à partir d’acides α-aminés, ont été étudiés. Dans un premier temps un protocole de synthèse de morpholine-2,5-diones, commun à plusieurs acides α-aminés a été développé. Celui-ci a pu être mis en application sur un mélange d’acides aminés, afin de produire des mélanges de morpholine-2,5-diones. Ces dernières ont alors été copolymérisées à l’aide de différents catalyseurs afin de démontrer le potentiel des copolydepsipeptides pour la valorisation de biomasse protéinée. Dans un second temps, la polymérisation organocatalysée de la 3S-(isobutyl)morpholine-2,5-dione et sa copolymérisation avec le lactide ont été étudiées en employant la 1,8-diazabicyclo[5,4,0]undéc-7-ène et une thiourée comme système co-catalytique. Celui-ci permet de synthétiser les polydepsipeptides et copolymères poly(depsipeptide-r-lactide)s de manière contrôlée. Finalement, afin de réduire l’impact environnemental de la synthèse des morpholine-2,5-diones et des polydepsipeptides, nous avons fait appel à la synthèse assistée par mécanochimie et par micro-ondes. A l’aide de ces techniques, une gamme de morpholine-2,5-diones a pu être produite avec bien plus de rapidité et de facilité qu’en solution, en utilisant considérablement moins de solvants et d’énergie. La mécanochimie a également été employée avec succès pour la polymérisation organocatalysée de la 3S-(isobutyl)morpholine-2,5-dione et pour sa copolymérisation avec le lactide. Cette étude permet une comparaison directe entre la ROP en solution et la ROP assistée par mécanochimie qui est, à ce jour, un domaine largement inexploré
Over the course of this work, the elaboration and the organocatalysed polymerisation and copolymerisation of morpholine-2,5-diones, monomers derived from α-amino acids, was studied. Firstly, an experimental protocol was developed, allowing for the synthesis of morpholine-2,5-diones from different amino-acids. The latter was then used for the production of a mix of morpholine-2,5-diones from a blend of amino-acids. This mixture of morpholine-2,5-diones was subsequently copolymerised using different catalysts. Next, the ring-opening polymerisation of 3S-(isobutyl)morpholine-2,5-dione as well as its copolymerisation with lactide was investigated via organocatalysis using 1,8-diazabicyclo[5.4.0]undec-7-ene and a thiourea co-catalyst. This catalytic system granted great control over the synthesis of polydepsipeptides and poly(depsipeptide-r-lactide) copolymers. Finally, with the aim of reducing the environmental impact of the different reactions developed herein, mechanochemical and microwave-based procedures were investigated. Using these techniques, a range of morpholine-2,5-diones were successfully produced in a much simpler and faster manner whilst using considerably less solvent and energy. Mechanochemistry also proved successful for the organocatalysed ring-opening polymerisation of 3S-(isobutyl)morpholine-2,5-dione and its copolymerisation with lactide. This study grants access to the direct comparison between solution and mechanochemical based ROPs which is, to date, a mostly unexplored field
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2

Feng, Yakai [Verfasser]. "Synthese und Charakterisierung von bioabbaubaren Polymeren auf der Basis von Polydepsipeptiden = Synthesis and characterization of biodegradable polymers based on polydepsipeptides / vorgelegt von Yakai Feng." 2000. http://d-nb.info/961960450/34.

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Book chapters on the topic "Polydepsipeptides"

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Abdelmelek, Mena, Mary Nguyen, Valerie Bradford, Brent Iverson, and Laura Suggs. "Synthesis of Morpholine-2,5-dione Monomers for the Preparation of Polydepsipeptides." In ACS Symposium Series, 185–96. Washington, DC: American Chemical Society, 2010. http://dx.doi.org/10.1021/bk-2010-1054.ch010.

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Samyn, C., M. Van Beylen, and A. Maes. "Biodegradable Polymers: Polydepsipeptides." In Encyclopedia of Biomedical Polymers and Polymeric Biomaterials, 732–38. Taylor & Francis, 2015. http://dx.doi.org/10.1081/e-ebpp-120051878.

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Dijkstra, P. J., M. J. D. Eenink, and J. Feijen. "Alpha-Hydroxy Acid Based Biodegradable Polymers Poly(L-Lactide) And Polydepsipeptides." In Degradable Materials, 99–142. CRC Press, 2018. http://dx.doi.org/10.1201/9781351071321-5.

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Ouchi, T., Y. Okamoto, M. Shiratani, M. Hirao, M. Jinno, and Y. Ohya. "Synthesis of polydepsipeptide with pendant carboxylic acid groups and its hydrolysis behavior." In Studies in Polymer Science, 528–33. Elsevier, 1994. http://dx.doi.org/10.1016/b978-0-444-81708-2.50061-0.

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