Repository logo

Infoscience

  • English
  • French
Log In
Logo EPFL, École polytechnique fédérale de Lausanne

Infoscience

  • English
  • French
Log In
  1. Home
  2. Academic and Research Output
  3. Journal articles
  4. Chemoenzymic synthesis of enantiomerically pure 4-fluoro-3-nitro and 3-fluoro-4-nitro phenylalanine
 
research article

Chemoenzymic synthesis of enantiomerically pure 4-fluoro-3-nitro and 3-fluoro-4-nitro phenylalanine

Vergne, Caroline
•
Bois-Choussy, Michele
•
Ouazzani, Jamal
Show more
1997
Tetrahedron: Asymmetry

Enantiomerically pure L- and D-4-fluoro-3-nitrophenylalanines and L- and D-3-fluoro-4-nitrophenylalanines were obtained from their corresponding racemates via enzymic resoln. [on SciFinder (R)]

  • Details
  • Metrics
Type
research article
DOI
10.1016/S0957-4166(96)00524-1
Author(s)
Vergne, Caroline
Bois-Choussy, Michele
Ouazzani, Jamal
Beugelmans, Rene
Zhu, Jieping  
Date Issued

1997

Published in
Tetrahedron: Asymmetry
Volume

8

Issue

3

Start page

391

End page

398

Subjects

Resolution (enzymic; chemoenzymic synthesis of enantiomerically pure fluoronitrophenylalanines)

•

fluoronitrophenylalanine enantiopure chemoenzymic synthesis; enzymic resoln racemic fluoronitrophenylalanine

Note

CAN 126:251367

34-2

Amino Acids, Peptides, and Proteins

Institut de Chimie des Substances Naturelles, CNRS,Gif-Sur-Yvette,Fr.

Journal

written in English.

188624-28-4P; 188624-29-5P Role: BPN (Biosynthetic preparation), RCT (Reactant), BIOL (Biological study), PREP (Preparation), RACT (Reactant or reagent) (chemoenzymic synthesis of enantiomerically pure fluoronitrophenylalanines); 9014-01-1 (Subtilisin) Role: CAT (Catalyst use), USES (Uses) (chemoenzymic synthesis of enantiomerically pure fluoronitrophenylalanines); 188624-30-8P; 188624-31-9P Role: PUR (Purification or recovery), RCT (Reactant), PREP (Preparation), RACT (Reactant or reagent) (chemoenzymic synthesis of enantiomerically pure fluoronitrophenylalanines); 15017-52-4; 131858-37-2 Role: RCT (Reactant), RACT (Reactant or reagent) (chemoenzymic synthesis of enantiomerically pure fluoronitrophenylalanines); 20367-99-1P; 188624-22-8P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (chemoenzymic synthesis of enantiomerically pure fluoronitrophenylalanines); 160247-85-8P; 169825-21-2P; 173775-54-7P; 178208-42-9P; 178744-39-3P; 188624-32-0P; 188624-33-1P; 188624-34-2P Role: SPN (Synthetic preparation), PREP (Preparation) (chemoenzymic synthesis of enantiomerically pure fluoronitrophenylalanines); 370-54-7P; 188624-23-9P; 188624-24-0P; 188624-25-1P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (racemic; chemoenzymic synthesis of enantiomerically pure fluoronitrophenylalanines); 188624-26-2P; 188624-27-3P Role: SPN (Synthetic preparation), PREP (Preparation) (racemic; chemoenzymic synthesis of enantiomerically pure fluoronitrophenylalanines)

Editorial or Peer reviewed

REVIEWED

Written at

OTHER

EPFL units
LSPN  
Available on Infoscience
November 25, 2010
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/58545
Logo EPFL, École polytechnique fédérale de Lausanne
  • Contact
  • infoscience@epfl.ch

  • Follow us on Facebook
  • Follow us on Instagram
  • Follow us on LinkedIn
  • Follow us on X
  • Follow us on Youtube
AccessibilityLegal noticePrivacy policyCookie settingsEnd User AgreementGet helpFeedback

Infoscience is a service managed and provided by the Library and IT Services of EPFL. © EPFL, tous droits réservés