ω-Transaminase-catalyzed asymmetric synthesis of unnatural amino acids using isopropylamine as an amino donor
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Title
ω-Transaminase-catalyzed asymmetric synthesis of unnatural amino acids using isopropylamine as an amino donor
Authors
Keywords
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Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 11, Issue 40, Pages 6929
Publisher
Royal Society of Chemistry (RSC)
Online
2013-07-30
DOI
10.1039/c3ob40495a
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- Molecular determinants for substrate selectivity of ω-transaminases
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- Update 1 of: Enantioselective Enzymatic Desymmetrizations in Organic Synthesis
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- One-Pot Conversion of L-Threonine into L-Homoalanine: Biocatalytic Production of an Unnatural Amino Acid from a Natural One
- (2010) Eulsoo Park et al. ADVANCED SYNTHESIS & CATALYSIS
- Transaminations with isopropyl amine: equilibrium displacement with yeast alcohol dehydrogenase coupled to in situ cofactor regeneration
- (2010) Karim Engelmark Cassimjee et al. CHEMICAL COMMUNICATIONS
- Biocatalytic Asymmetric Synthesis of Chiral Amines from Ketones Applied to Sitagliptin Manufacture
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- ω-Transaminases for the synthesis of non-racemic α-chiral primary amines
- (2010) Dominik Koszelewski et al. TRENDS IN BIOTECHNOLOGY
- Peptide drugs to target G protein-coupled receptors
- (2010) Kathrin Bellmann-Sickert et al. TRENDS IN PHARMACOLOGICAL SCIENCES
- Scaleable catalytic asymmetric Strecker syntheses of unnatural α-amino acids
- (2009) Stephan J. Zuend et al. NATURE
- A Multidisciplinary Approach Toward the Rapid and Preparative-Scale Biocatalytic Synthesis of Chiral Amino Alcohols: A Concise Transketolase-/ω-Transaminase-Mediated Synthesis of (2S,3S)-2-Aminopentane-1,3-diol
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- Chemo-enzymatic deracemization methods for the preparation of enantiopure non-natural α-amino acids
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