Gotowa bibliografia na temat „Polydepsipeptides”
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Artykuły w czasopismach na temat "Polydepsipeptides"
Feng, Yakai, i Jintang Guo. "Biodegradable Polydepsipeptides". International Journal of Molecular Sciences 10, nr 2 (13.02.2009): 589–615. http://dx.doi.org/10.3390/ijms10020589.
Pełny tekst źródłaMAMMI, STEFANO, i MURRAY GOODMAN. "Polydepsipeptides. 13". International Journal of Peptide and Protein Research 28, nr 1 (12.01.2009): 29–44. http://dx.doi.org/10.1111/j.1399-3011.1986.tb03227.x.
Pełny tekst źródłaDijkstra, Pieter J., i Jan Feijen. "Synthetic pathways to polydepsipeptides". Macromolecular Symposia 153, nr 1 (marzec 2000): 67–76. http://dx.doi.org/10.1002/1521-3900(200003)153:1<67::aid-masy67>3.0.co;2-f.
Pełny tekst źródłaBecktel, W. J., G. Wouters, D. M. Simmons i Murray Goodman. "Polydepsipeptides. 11. Conformational analysis of polydepsipeptides containing methyl, isopropyl, and isobutyl side chains". Macromolecules 18, nr 4 (lipiec 1985): 630–34. http://dx.doi.org/10.1021/ma00146a009.
Pełny tekst źródłaDijkstra, Pieter J., i Jan Feijen. "ChemInform Abstract: Synthetic Pathways to Polydepsipeptides". ChemInform 31, nr 47 (21.11.2000): no. http://dx.doi.org/10.1002/chin.200047264.
Pełny tekst źródłaMammi, Stefano, i Murray Goodman. "Polydepsipeptides. A systematic investigation of guest-host effects". Journal of Peptide Science 11, nr 5 (2005): 273–77. http://dx.doi.org/10.1002/psc.665.
Pełny tekst źródłaOhya, Yuichi, Hidetoshi Yamamoto, Koji Nagahama i 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, nr 15 (12.06.2009): 3892–903. http://dx.doi.org/10.1002/pola.23456.
Pełny tekst źródłaYoshida, Masaru, Masaharu Asano, Minoru Kumakura, Ryoichi Katakai, Tooru Mashimo, Hisako Yuasa, Kyoichi Imai i Hidetoshi Yamanaka. "Sequential polydepsipeptides as biodegradable carriers for drug delivery systems". Journal of Biomedical Materials Research 24, nr 9 (wrzesień 1990): 1173–84. http://dx.doi.org/10.1002/jbm.820240904.
Pełny tekst źródłaOuchi, Tasuro, Tatsuya Nozaki, Yoshifumi Okamoto, Masahiro Shiratani i Yuichi Ohya. "Synthesis and enzymatic hydrolysis of polydepsipeptides with functionalized pendant groups". Macromolecular Chemistry and Physics 197, nr 6 (czerwiec 1996): 1823–33. http://dx.doi.org/10.1002/macp.1996.021970604.
Pełny tekst źródłaYoshida, Masaru, Masaharu Asano, Minoru Kumakura, Ryoichi Katakai, Tooru Mashimo, Hisako Yuasa i Hidetoshi Yamanaka. "Sequential polydepsipeptides containing tripeptide sequences and α-hydroxy acids as biodegradable carriers". European Polymer Journal 27, nr 3 (styczeń 1991): 325–29. http://dx.doi.org/10.1016/0014-3057(91)90113-3.
Pełny tekst źródłaRozprawy doktorskie na temat "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.
Pełny tekst źródłaOver 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.
Pełny tekst źródłaCzęści książek na temat "Polydepsipeptides"
Abdelmelek, Mena, Mary Nguyen, Valerie Bradford, Brent Iverson i Laura Suggs. "Synthesis of Morpholine-2,5-dione Monomers for the Preparation of Polydepsipeptides". W ACS Symposium Series, 185–96. Washington, DC: American Chemical Society, 2010. http://dx.doi.org/10.1021/bk-2010-1054.ch010.
Pełny tekst źródłaSamyn, C., M. Van Beylen i A. Maes. "Biodegradable Polymers: Polydepsipeptides". W Encyclopedia of Biomedical Polymers and Polymeric Biomaterials, 732–38. Taylor & Francis, 2015. http://dx.doi.org/10.1081/e-ebpp-120051878.
Pełny tekst źródłaDijkstra, P. J., M. J. D. Eenink i J. Feijen. "Alpha-Hydroxy Acid Based Biodegradable Polymers Poly(L-Lactide) And Polydepsipeptides". W Degradable Materials, 99–142. CRC Press, 2018. http://dx.doi.org/10.1201/9781351071321-5.
Pełny tekst źródłaOuchi, T., Y. Okamoto, M. Shiratani, M. Hirao, M. Jinno i Y. Ohya. "Synthesis of polydepsipeptide with pendant carboxylic acid groups and its hydrolysis behavior". W 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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