Pronase in amino acid technology: Optical resolution of nonproteinogenic ?-amino acids-Reference-Cited by-同舟云学术

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Pronase in amino acid technology: Optical resolution of nonproteinogenic ?-amino acids

Published:1994 Issue:6 Volume:6 Page:472-478
ISSN:0899-0042
Container-title:Chirality
language:en
Short-container-title:Chirality

Author:

Pugniere Martine,Domergue Nicole,Castro Bertrand,Inserm Aldo Previero

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

Reference11 articles.

1. New effective gonadotropin releasing hormone antagonists with minimal potency for histamine release in vitro

2. eds. Asymmetric Synthesis, Construction of Chiral Molecules Using Amino Acids. New York: Wiley-Intersciences, 1987: 1-393.

3. A PROTEOLYTIC ENZYME OF STREPTOMYCES GRISEUS

4. Proteases as catalysts of enantioselective α-amino ester hydrolysis: 3. Pronase-catalysed hydrolysis of methyl esters of leucine, phenylalanine and valine

5. Enzymatic synthesis of side chain benzyl esters of L-α-amino dicarboxylic acids

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1. Naphthyl-l-α-amino acids via chemo-enzymatic dynamic kinetic resolution;Tetrahedron: Asymmetry;2012-07

2. Enzymatic approach to both enantiomers of N-Boc hydrophobic amino acids;Tetrahedron: Asymmetry;2006-08

3. Engineering aromaticL-amino acid transaminase for the asymmetric synthesis of constrained analogs ofL-phenylalanine;Biotechnology and Bioengineering;2006

4. The Preparation of Single Enantiomer 2-Naphthylalanine Derivatives Using Rhodium−Methyl BoPhoz-catalyzed Asymmetric Hydrogenation;Organic Process Research & Development;2005-05-24

5. Asymmetric synthesis ofL-homophenylalanine by equilibrium-shift using recombinant aromaticL-amino acid transaminase;Biotechnology and Bioengineering;2003-05-21

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