Enzymatic synthesis of L-6-hydroxynorleucine
- Author
- HANSON, R. L1 ; SCHWINDEN, M. D2 ; SZARKA, L. J1 ; BANERJEE, A1 ; BRZOZOWSKI, D. B1 ; CHEN, B.-C3 ; PATEL, B. P2 ; MCNAMEE, C. G1 ; KODERSHA, G. A3 ; KRONENTHAL, D. R2 ; PATEL, R. N1
[1] Department of Microbial Technology, Bristol-Myers Squibb, One Squibb Drive, New Brunswick, NJ 08903, United States
[2] Chemical Process Research, Bristol-Myers Squibb, P.O. Box 4000, Princeton, NJ 08540, United States
[3] Chemical Process Development, Bristol-Myers Squibb, One Squibb Drive, New Brunswick, NJ 08903, United States - Issue title
- New Methods for the Discovery and Implementation of Novel Biocatalysts
- Author (monograph)
- DEMIRJIAN, David C (Editor)1
[1] ThermoGen, Inc., Chicago, IL 60612, United States - Source
Bioorganic & medicinal chemistry. 1999, Vol 7, Num 10, pp 2247-2252 ; ref : 19 ref
- ISSN
- 0968-0896
- Scientific domain
- Biochemistry, molecular biology, biophysics; Pharmacology drugs
- Publisher
- Elsevier Science, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Amination Aminoalcool Composé aliphatique Cétoacide D-Amino-acid oxidase Enantiosélectivité Glutamate dehydrogenase Hydrolyse Pureté optique Réaction enzymatique Réduction chimique Stéréoisomère L Synthèse chimique α-Aminoacide Caproïque acide(6-hydroxy-2-oxo) Hexanoïque acide(6-hydroxy-2-oxo) Hydantoïne(5-[4-hydroxybutyl]) Norleucine(6-hydroxy) Enzyme Oxidoreductases
- Keyword (en)
- Amination Aminoalcohol Aliphatic compound Ketoacid D-Amino-acid oxidase Enantioselectivity Glutamate dehydrogenase Hydrolysis Optical purity Enzymatic reaction Chemical reduction L stereoisomer Chemical synthesis α-Aminoacid Enzyme Oxidoreductases
- Keyword (es)
- Aminación Aminoalcohol Compuesto alifático Cetoácido D-Amino-acid oxidase Enantioselectividad Glutamate dehydrogenase Hidrólisis Pureza óptica Reacción enzimática Reducción química Estereoisómero L Síntesis química α-Aminoácido Enzima Oxidoreductases
- 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
- 1213692
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/S0968-0896(99)00158-3 
https://dx.doi.org/10.1016/S0968-0896(99)00158-3
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