scholarly journals Developing Multicompartment Biopolymer Hydrogel Beads for Tandem Chemoenzymatic One-Pot Process

Catalysts ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 547 ◽  
Author(s):  
Jan Pauly ◽  
Harald Gröger ◽  
Anant V. Patel

Chemoenzymatic processes have been gaining interest to implement sustainable reaction steps or even create new synthetic routes. In this study, we combined Grubbs’ second-generation catalyst with pig liver esterase and conducted a chemoenzymatic one-pot process in a tandem mode. To address sustainability, we encapsulated the catalysts in biopolymer hydrogel beads and conducted the reaction cascade in an aqueous medium. Unfortunately, conducting the process in tandem led to increased side product formation. 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.

2015 ◽  
Vol 19 (12) ◽  
pp. 2034-2038 ◽  
Author(s):  
Philipp Süss ◽  
Sonja Borchert ◽  
Janine Hinze ◽  
Sabine Illner ◽  
Jan von Langermann ◽  
...  

Author(s):  
D. Jonathan Bennett ◽  
Kirsteen I. Buchanan ◽  
Andrew Cooke ◽  
Ola Epemolu ◽  
Niall M. Hamilton ◽  
...  

1985 ◽  
Vol 63 (2) ◽  
pp. 452-456 ◽  
Author(s):  
J. Bryan Jones ◽  
R. Scott Hinks ◽  
Philip G. Hultin

Preparative-scale pig liver esterase-catalyzed hydrolyses of five-membered ring meso-1,3-diesters are enantiotopically selective. While pro-S enantiotopic selectivity is exhibited in each case, the absolute configuration sense of the hydrolysis in the cyclopentyl series is opposite to that of both the tetrahydrofuranyl and tetrahydrothiophenyl diesters. The enantiomeric excess levels induced are in the 34–46% range.


1989 ◽  
Vol 54 (21) ◽  
pp. 5115-5122 ◽  
Author(s):  
Hans Joachim Gais ◽  
Gerd Buelow ◽  
Andrzej Zatorski ◽  
Mathias Jentsch ◽  
Peter Maidonis ◽  
...  

Tetrahedron ◽  
2008 ◽  
Vol 64 (37) ◽  
pp. 8947-8951 ◽  
Author(s):  
Long Yi ◽  
Li Cao ◽  
Liangliang Liu ◽  
Zhen Xi

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