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• The New Plastics Economy: Rethinking the future of plastics, World Econ. Forum. (2016).
• Jambeck, J.R., Geyer, R., Wilcox, C., Siegler, T.R., Perryman, M., Andrady, A., Narayan, R., Law, K.L., Plastic waste inputs from land into the ocean. Science 347 (2015), 768–771, 10.1126/science.1260352.
• Castro-Aguirre, E., Iñiguez-Franco, F., Samsudin, H., Fang, X., Auras, R., Poly(lactic acid)—Mass production, processing, industrial applications, and end of life. Adv. Drug Deliv. Rev. 107 (2016), 333–366, 10.1016/j.addr.2016.03.010.
• Becker, J.M., Pounder, R.J., Dove, A.P., Synthesis of poly(lactide)s with modified thermal and mechanical properties. Macromol. Rapid Commun. 31 (2010), 1923–1937, 10.1002/marc.201000088.
• Lim, L.-T., Auras, R., Rubino, M., Processing technologies for poly(lactic acid). Prog. Polym. Sci. 33 (2008), 820–852, 10.1016/j.progpolymsci.2008.05.004.
• Auras, R., Harte, B., Selke, S., An overview of polylactides as packaging materials. Macromol. Biosci. 4 (2004), 835–864, 10.1002/mabi.200400043.
• Slomkowski, S., Penczek, S., Duda, A., Polylactides-an overview: polylactides-an overview. Polym. Adv. Technol. 25 (2014), 436–447, 10.1002/pat.3281.
• Jacobsen, S., Fritz, H.G., Degée, P., Dubois, P., Jérôme, R., Single-step reactive extrusion of PLLA in a corotating twin-screw extruder promoted by 2-ethylhexanoic acid tin(II) salt and triphenylphosphine. Polymer 41 (2000), 3395–3403, 10.1016/S0032-3861(99)00507-8.
• Tanzi, M.C., Verderio, P., Lampugnani, M.G., Resnati, M., Dejana, E., Sturani, E., Cytotoxicity of some catalysts commonly used in the synthesis of copolymers for biomedical use. J. Mater. Sci. Mater. Med. 5 (1994), 393–396, 10.1007/BF00058971.
• Kamber, N.E., Jeong, W., Waymouth, R.M., Pratt, R.C., Lohmeijer, B.G.G., Hedrick, J.L., Organocatalytic ring-opening polymerization. Chem. Rev. 107 (2007), 5813–5840, 10.1021/cr068415b.
• Ottou, W.N., Sardon, H., Mecerreyes, D., Vignolle, J., Taton, D., Update and challenges in organo-mediated polymerization reactions. Prog. Polym. Sci. 56 (2016), 64–115, 10.1016/j.progpolymsci.2015.12.001.
• Matsumura, S., Mabuchi, K., Toshima, K., Lipase-catalyzed ring-opening polymerization of lactide. Macromol. Rapid Commun. 18 (1997), 477–482, 10.1002/marc.1997.030180604.
• Matsumura, S., Mabuchi, K., Toshima, K., Novel ring-opening polymerization of lactide by lipase. Macromol. Symp. 130 (1998), 285–304, 10.1002/masy.19981300125.
• Fujioka, M., Hosoda, N., Nishiyama, S., Noguchi, H., Shoji, A., Kumar, D.S., Katsuraya, K., Ishii, S., Yoshida, Y., One-pot enzymatic synthesis of poly(L,L-lactide) by immobilized lipase catalyst. FIBER 62 (2006), 63–65, 10.2115/fiber.62.63.
• Yoshizawa-Fujita, M., Saito, C., Takeoka, Y., Rikukawa, M., Lipase-catalyzed polymerization of L-lactide in ionic liquids. Polym. Adv. Technol. 19 (2008), 1396–1400, 10.1002/pat.1217.
• Mena, M., López-Luna, A., Shirai, K., Tecante, A., Gimeno, M., Bárzana, E., Lipase-catalyzed synthesis of hyperbranched poly-L-lactide in an ionic liquid. Bioprocess Biosyst. Eng. 36 (2013), 383–387, 10.1007/s00449-012-0792-3.
• Nederberg, F., Connor, E.F., Möller, M., Glauser, T., Hedrick, J.L., New paradigms for organic catalysts: the first organocatalytic living polymerization. Angew. Chem. Int. Ed. 40 (2001), 2712–2715, 10.1002/1521-3773(20010716)40:14<2712::AID-ANIE2712>3.0.CO;2-Z.
• Guillerm, B., Lemaur, V., Ernould, B., Cornil, J., Lazzaroni, R., Gohy, J.-F., Dubois, P., Coulembier, O., A one-pot two-step efficient metal-free process for the generation of PEO-b-PCL-b-PLA amphiphilic triblock copolymers. RSC Adv., 4, 2014, 10028, 10.1039/c3ra47204c.
• Sweet, D.V., Regist. Toxic Eff. Chem. Subst., 1985.
• Katiyar, V., Nanavati, H., Ring-opening polymerization of L-lactide using N-heterocyclic molecules: mechanistic, kinetics and DFT studies. Polym. Chem., 1, 2010, 1491, 10.1039/c0py00125b.
• Myers, M., Connor, E.F., Glauser, T., Möck, A., Nyce, G., Hedrick, J.L., Phosphines: Nucleophilic organic catalysts for the controlled ring-opening polymerization of lactides. J. Polym. Sci. Part Polym. Chem. 40 (2002), 844–851, 10.1002/pola.10168.
• Buckler, S.A., Autoxidation of trialkylphosphines. J. Am. Chem. Soc. 84 (1962), 3093–3097, 10.1021/ja00875a011.
• Dubois, P., Coulembier, O., Delcourt, C., Bulk polymerization of (L,L)-lactide using non-organometallic triazolium carbene: limited advantages. Open Macromol. J. 1 (2007), 1–5, 10.2174/1874343900701010001.
• Wang, C., Li, H., Zhao, X., Ring opening polymerization of L-lactide initiated by creatinine. Biomaterials 25 (2004), 5797–5801, 10.1016/j.biomaterials.2004.01.030.
• Li, H., Wang, C., Yue, J., Zhao, X., Bai, F., Living ring-opening polymerization of lactides catalyzed by guanidinium acetate. J. Polym. Sci. Part Polym. Chem. 42 (2004), 3775–3781, 10.1002/pola.20275.
• Kricheldorf, H.R., Lomadze, N., Schwarz, G., Cyclic polylactides by imidazole-catalyzed polymerization of L-lactide. Macromolecules 41 (2008), 7812–7816, 10.1021/ma801519t.
• Nogueira, G., Favrelle, A., Bria, M., Prates Ramalho, J.P., Mendes, P.J., Valente, A., Zinck, P., Adenine as an organocatalyst for the ring-opening polymerization of lactide: scope, mechanism and access to adenine-functionalized polylactide. React. Chem. Eng. 1 (2016), 508–520, 10.1039/C6RE00061D.
• Lewinski, P., Sosnowski, S., Penczek, S., L-lactide polymerization – living and controlled – catalyzed by initiators: Hydroxyalkylated organic bases. Polymer 108 (2017), 265–271, 10.1016/j.polymer.2016.11.070.
• Bednarek, M., Basko, M., Biedron, T., Wojtczak, E., Michalski, A., Polymerization of lactide initiated by primary amines and catalyzed by a protic acid. Eur. Polym. J. 71 (2015), 380–388, 10.1016/j.eurpolymj.2015.08.012.
• Saito, T., Aizawa, Y., Tajima, K., Isono, T., Satoh, T., Organophosphate-catalyzed bulk ring-opening polymerization as an environmentally benign route leading to block copolyesters, end-functionalized polyesters, and polyester-based polyurethane. Polym. Chem. 6 (2015), 4374–4384, 10.1039/C5PY00533G.
• Bourissou, D., Martin-Vaca, B., Dumitrescu, A., Graullier, M., Lacombe, F., Controlled cationic polymerization of lactide. Macromolecules 38 (2005), 9993–9998, 10.1021/ma051646k.
• Susperregui, N., Delcroix, D., Martin-Vaca, B., Bourissou, D., Maron, L., Ring-opening polymerization of ε-caprolactone catalyzed by sulfonic acids: computational evidence for bifunctional activation. J. Org. Chem. 75 (2010), 6581–6587, 10.1021/jo101346t.
• Delcroix, D., Couffin, A., Susperregui, N., Navarro, C., Maron, L., Martin-Vaca, B., Bourissou, D., Phosphoric and phosphoramidic acids as bifunctional catalysts for the ring-opening polymerization of ε-caprolactone: a combined experimental and theoretical study. Polym. Chem., 2, 2011, 2249, 10.1039/c1py00210d.
• Li, H., Zhang, S., Jiao, J., Jiao, Z., Kong, L., Xu, J., Li, J., Zuo, J., Zhao, X., Controlled synthesis of polylactides using biogenic creatinine carboxylate initiators. Biomacromol 10 (2009), 1311–1314, 10.1021/bm801479p.
• Oledzka, E., Sokolowski, K., Sobczak, M., Kolodziejski, W., Α-Amino acids as initiators of ε-caprolactone and L,L-lactide polymerization. Polym. Int. 60 (2011), 787–793, 10.1002/pi.3016.
• Coulembier, O., Josse, T., Guillerm, B., Gerbaux, P., Dubois, P., An imidazole-based organocatalyst designed for bulk polymerization of lactide isomers: inspiration from Nature. Chem. Commun. 48 (2012), 11695–11697, 10.1039/c2cc37061a.
• Kadota, J., Pavlović, D., Hirano, H., Okada, A., Agari, Y., Bibal, B., Deffieux, A., Peruch, F., Controlled bulk polymerization of L-lactide and lactones by dual activation with organo-catalytic systems. RSC Adv., 4, 2014, 14725, 10.1039/c4ra01239a.