Literature DB >> 30799035

Synthesis of (E)-α,β-unsaturated carboxylic esters derivatives from cyanoacetic acid via promiscuous enzyme-promoted cascade esterification/Knoevenagel reaction.

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.
Copyright © 2019 Elsevier Inc. All rights reserved.

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


  1 in total

1.  Promiscuous Lipase-Catalyzed Knoevenagel-Phospha-Michael Reaction for the Synthesis of Antimicrobial β-Phosphono Malonates.

Authors:  Jan Samsonowicz-Górski; Dominik Koszelewski; Paweł Kowalczyk; Paweł Śmigielski; Anastasiia Hrunyk; Karol Kramkowski; Aleksandra Wypych; Mateusz Szymczak; Rafał Lizut; Ryszard Ostaszewski
Journal:  Int J Mol Sci       Date:  2022-08-08       Impact factor: 6.208

  1 in total

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