The control of Novozym® 435 chemoselectivity and specificity by the solvents in acylation reactions of amino-alcohols-Reference-Cited by-同舟云学术

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The control of Novozym® 435 chemoselectivity and specificity by the solvents in acylation reactions of amino-alcohols

Published:2013-11 Issue: Volume:95 Page:99-110
ISSN:1381-1177
Container-title:Journal of Molecular Catalysis B: Enzymatic
language:en
Short-container-title:Journal of Molecular Catalysis B: Enzymatic

Author:

Le Joubioux Florian,Bridiau Nicolas,Ben Henda Yesmine,Achour Oussama,Graber Marianne,Maugard Thierry

Funder

Centre National de la Recherche Scientifique

French ANR (National Research Agency)

Publisher

Elsevier BV

Subject

Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis

Reference78 articles.

1. Lipase-Catalyzed Enantiomeric Resolution of Ceramides

2. Glycoside analogs of β-galactosylceramide, a novel class of small molecule antiviral agents that inhibit HIV-1 entry

3. Mechanisms involved in exogenous C2- and C6-ceramide-induced cancer cell toxicity

4. L. Lassalle, F. Yvergnaux, FR Patent 2,855,823 (2004).

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2. Excellence in Acrylation – Scope and Limitation of Glucosyl Imidazolium‐coated Novozym 435 Catalyzed (Meth)acryl Ester Synthesis;Chemistry – An Asian Journal;2023-12-08

3. Chemoselective Lipase-Catalyzed Synthesis of Amido Derivatives from 5-Hydroxymethylfurfurylamine;ACS Sustainable Chemistry & Engineering;2023-07-06

4. Step-by-Step Hybrid Conversion of Glucose to 5-acetoxymethyl-2-furfural Using Immobilized Enzymes and Cation Exchange Resin;Processes;2022-10-14

5. Effect of the acyl-group length on the chemoselectivity of the lipase-catalyzed acylation of propranolol—a computational study;Journal of Molecular Modeling;2021-06-11

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