| Literature DB >> 30799035 |
Monika Wilk1, Damian Trzepizur1, Dominik Koszelewski1, Anna Brodzka1, Ryszard Ostaszewski2.
Abstract
A new enzymatic protocol based on lipase-catalyzed cascade toward (E)-α,β-unsaturated carboxylic esters is presented. The proposed methodology consists of elementary organic processes starting from acetals and cyanoacetic acid leading to the formation of desired products in a cascade sequence. The combination of enzyme promiscuous abilities gives a new opportunity to synthesize complex molecules in the one-pot procedure. Results of studies on the influence of an enzyme type, solvent, and temperature on the cascade reaction course are reported. The presented methodology provides meaningful qualities such as significantly simplified process, excellent E-selectivity of obtained products and recycling of a biocatalyst.Entities:
Keywords: Acetal; Cascade reaction; Esterification; Knoevenagel condensation; Lipase; Multi-promiscuity
Year: 2019 PMID: 30799035 DOI: 10.1016/j.bioorg.2019.02.041
Source DB: PubMed Journal: Bioorg Chem ISSN: 0045-2068 Impact factor: 5.275