This work reports the first lipase-catalyzed reactions between substrates of different polarities using deep eutectic solvents as a medium. The model reaction consisted of a lipophilization process based on the alcoholysis of phenolic esters using immobilized Candida antarctica lipase B as a biocatalyst. Results showed that water could dramatically improve the lipase activity and change the reactivity of phenolic substrates. Indeed, very low conversions (<2%) were observed in pure DES, whereas in DES–water binary mixtures, quantitative conversions were achieved. After investigating the role of various parameters, such as the substrate concentration and ratio, pH or thermodynamic activity of water, the effect of the presence of water in pure DES based on urea or glycerol was discussed. In this paper, we propose new perspectives for the enzymatic modification of polar substrates using this novel generation of green, inexpensive and easy-to-handle solvents.

The chemo-enzymatic epoxidation of allylated gallic and vanillic acids with lipase B from Candida antarctica and aqueous hydrogen peroxide in the presence of caprylic acid was investigated. The use of 1 molar eq of caprylic acid and 1.8–2 molar eq of H₂O₂ per allylic double bond led to a high degree of conversion to epoxides (89% yield for allylated gallic acid and 87% yield for allylated vanillic acid) comparatively to the hazardous peracid mCPBA (1.5–3.2 molar eq per double bond allowed 75–85% yield). The epoxidized products obtained could be used in the formulation of novel bio-based epoxy resins.

The effect of the type of epoxidation processes of soybean oil on the characteristics of epoxidized soybean oils (ESOs), acrylated epoxidized soybean oils (AESOs), and acrylated epoxidized soybean oil – poly(methyl metacrylate) copolymers (AESO-co-PMMA) has been investigated. Two epoxidation processes were used: an in situ chemical epoxidation using hydrogen peroxide and formic acid, and a chemo-enzymatic epoxidation using 2 enzymes: Novozyme® 435 (CALB) and a homemade lipase/acyltransferase (CpLIP2). ESOs containing different numbers of epoxide groups/molecule were synthesized. A commercial ESO (Vikoflex® 7170) was employed and it had the highest number of epoxide groups. Acrylation of ESOs was carried out using acrylic acid, and copolymerized with a methyl methacrylate monomer. The chemo-enzymatic epoxidation produced high acid value, particularly from the CpLIP2 (!46–48%) and indicated the formation of epoxidized free fatty acids. In contrast, the ESO synthesized from the chemical epoxidation showed a very low acid value, < 0.6%. The AESOs synthesized from the CALB-based ESO and the chemical-based ESO showed a similar number of acrylate groups/molecule while that from the CpLIP2-based ESO showed a very low number of acrylate groups because the carboxylic groups from the epoxidized free fatty acids impeded the acrylation reaction. The lower the number of acrylate groups the lower was the crosslink density, the Tg, and the gel content in the AESO-co-PMMA copolymer