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Polylactides (PLAs) are at the forefront of biodegradable polymer research. These poly(α-hydroxy acids) can be prepared by polycondensation of lactic acid or ring-opening polymerization (ROP) of lactide, both routes typically involving metallic promoters. The first part of this review focuses on the recent achievements reported with metal-free systems via organocatalytic (nucleophilic, cationic and bifunctional) as well as enzymatic approaches. The second part of the review concerns the heterocyclic monomers that give access to poly(α-hydroxy acids) such as PLAs. Two complementary approaches will be discussed: substituted 1,4-dioxane-2,5-diones and synthetic equivalents thereof.
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Bourissou et al. (2007) studied this question.
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