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We then created core-shell beads with catalysts located in different compartments, which notably enhanced the selectivity towards the desired product compared to homogeneously distributing both catalysts within the matrix. Finally, we designed a specific large-sized bead with a diameter of 13.5 mm to increase the diffusion route of the Grubbs’ catalyst-containing shell. This design forced the ring-closing metathesis to occur first before the substrate could diffuse into the pig liver esterase-containing core, thus enhancing the selectivity to 75%. This study contributes to addressing reaction-related issues by designing specific immobilisates for chemoenzymatic processes.\r\n                ","lang":"eng"}],"language":[{"iso":"eng"}],"user_id":"231260","_id":"6976","intvolume":"         9","citation":{"alphadin":"<span style=\"font-variant:small-caps;\">Pauly, Jan</span> ; <span style=\"font-variant:small-caps;\">Gröger, Harald</span> ; <span style=\"font-variant:small-caps;\">Patel, Anant V. </span>: Developing Multicompartment Biopolymer Hydrogel Beads for Tandem Chemoenzymatic One-Pot Process. In: <i>Catalysts</i> Bd. 9, MDPI (2019), Nr. 6","ieee":"J. Pauly, H. Gröger, and A. V. 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