Literature DB >> 30014923

Promiscuous enzyme-catalyzed cascade reaction: Synthesis of xanthone derivatives.

Yajie Fu1, Bingbing Fan1, Hongyue Chen1, He Huang1, Yi Hu2.   

Abstract

Based on the screening of biocatalysts and reaction conditions including organic solvent, water content, lipase loading, reaction temperature and time, lipase TLIM exhibited the prominent promiscuity for the Knoevenagel-Michael cascade reactions of 1, 3-diketones with aromatic aldehydes to synthesize xanthone derivatives. This procedure provides satisfactory advantages such as environmental begin, simple work-up, generality, obtaining in excellent yields (80-97%), and potential for recycling of biocatalyst.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Aromatic aldehyde; Catalysis; Knoevenagel condensation; Lipase; Xanthone

Mesh:

Substances:

Year:  2018        PMID: 30014923     DOI: 10.1016/j.bioorg.2018.06.034

Source DB:  PubMed          Journal:  Bioorg Chem        ISSN: 0045-2068            Impact factor:   5.275


  1 in total

1.  Enzymatic approach to cascade synthesis of bis(indolyl)methanes in pure water.

Authors:  Yajie Fu; Zeping Lu; Ke Fang; Xinyi He; Huajin Xu; Yi Hu
Journal:  RSC Adv       Date:  2020-03-16       Impact factor: 3.361

  1 in total

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