The control of Novozym® 435 chemoselectivity and specificity by the solvents in acylation reactions of amino-alcohols
- Author
- LE JOUBIOUX, Florian1 ; BRIDIAU, Nicolas1 ; BEN HENDA, Yesmine1 ; ACHOUR, Oussama1 ; GRABER, Marianne1 ; MAUGARD, Thierry1
[1] UMR 7266 CNRS-ULR, LIENSs, Equipe Approches Moléculaires, Environnement-Santé, Université de La Rochelle. Avenue Michel Crépeau, 17042 La Rochelle, France - Source
Journal of molecular catalysis. B, Enzymatic. 2013, Vol 95, pp 99-110, 12 p ; ref : 78 ref
- ISSN
- 1381-1177
- Scientific domain
- Biotechnology
- Publisher
- Elsevier, Amsterdam
- Publication country
- Netherlands
- Document type
- Article
- Language
- English
- Author keyword
- Chemoselectivity Ionic liquid N-Acylation Novozym® 435 O-Acylation Organic solvent
- Keyword (fr)
- Acylation Alcool Chimiosélectivité Liquide ionique Solvant organique Spécificité
- Keyword (en)
- Acylation Alcohol Chemoselectivity Ionic liquid Organic solvent Specificity
- Keyword (es)
- Acilación Alcohol Quimioselectividad Líquido iónico Solvente orgánico Especificidad
- Classification
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A31 Biotechnology / 002A31C Methods. Procedures. Technologies / 002A31C06 Bioconversions. Hemisynthesis
- Discipline
- Biotechnology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 27561845
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1016/j.molcatb.2013.06.002 
https://dx.doi.org/10.1016/j.molcatb.2013.06.002
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