Добірка наукової літератури з теми "Polydepsipeptides"
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Статті в журналах з теми "Polydepsipeptides"
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.
Повний текст джерелаMAMMI, 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.
Повний текст джерелаDijkstra, 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.
Повний текст джерелаBecktel, 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.
Повний текст джерелаDijkstra, 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.
Повний текст джерелаMammi, 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.
Повний текст джерелаOhya, 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.
Повний текст джерелаYoshida, 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.
Повний текст джерелаOuchi, 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.
Повний текст джерелаYoshida, Masaru, Masaharu Asano, Minoru Kumakura, Ryoichi Katakai, Tooru Mashimo, Hisako Yuasa та Hidetoshi Yamanaka. "Sequential polydepsipeptides containing tripeptide sequences and α-hydroxy acids as biodegradable carriers". European Polymer Journal 27, № 3 (січень 1991): 325–29. http://dx.doi.org/10.1016/0014-3057(91)90113-3.
Повний текст джерелаДисертації з теми "Polydepsipeptides"
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.
Повний текст джерелаOver 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
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.
Повний текст джерелаЧастини книг з теми "Polydepsipeptides"
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.
Повний текст джерелаSamyn, 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.
Повний текст джерелаDijkstra, 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.
Повний текст джерелаOuchi, 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.
Повний текст джерела