Skip to search formSkip to main contentSkip to account menu

2-amino-1,3,4-butanetriol

Known as: syn-2-amino-1,3,4-butanetriol 
National Institutes of Health

Related topics

Related topics

1 relation

Broader (1)

Amino Alcohols

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Whole cell biosynthetic activity of Komagataella phaffii (Pichia pastoris) GS115 strains engineered with transgenes encoding Chromobacterium violaceum ω‐transaminase alone or combined with native…
Whole cell biocatalysis is an ideal tool for biotransformations that demand enzyme regeneration or robustness to fluctuating pH… 
2019
2019
Whole cell biosynthesis of 1-methyl-3-phenylpropylamine and 2-amino-1,3,4-butanetriol using Komagataella phaffii (Pichia pastoris) strain BG-10 engineered with a transgene encoding Chromobacterium…
Highly Cited
2013
Highly Cited
2013
Characterization and multi-step transketolase-ω-transaminase bioconversions in an immobilized enzyme microreactor (IEMR) with packed tube.
2013
2013
haracterization and multi-step transketolase-- transaminase ioconversions in an immobilized enzyme microreactor ( IEMR ) with acked tube
The concept of de novo metabolic engineering through novel synthetic pathways offers new directions for multi-step enzymatic… 
Highly Cited
2011
Highly Cited
2011
Immobilised enzyme microreactor for screening of multi-step bioconversions: characterisation of a de novo transketolase-ω-transaminase pathway to synthesise chiral amino alcohols.
2007
2007
One-pot synthesis of amino-alcohols using a de-novo transketolase and beta-alanine: pyruvate transaminase pathway in Escherichia coli.
Biocatalysis continues to emerge as a powerful technique for the efficient synthesis of optically pure pharmaceuticals that are… 
2001
2001
Orthogonally protected, enantiopure syn-2-amino-1,3,4-butanetriol: a general building block for syn-amino alcohols.
  • S. KwonS. Ko
  • Journal of Organic Chemistry
  • 2001
  • Corpus ID: 40558994
2000
2000
(1S)-1-[(4R)-2,2-dimethyl-1,3-dioxolan+-4-yl][-2-hydroxyethylamm onium benzoate, a versatile building block for chiral 2-aminoalkanols: concise synthesis and application to nelfinavir, a potent HIV…
A concise synthesis of a versatile chiral C4 building block for 2-aminoalkanols, (1S)-1-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2… 
Highly Cited
1999
Highly Cited
1999
Catalytic Asymmetric Aminolysis of 3,5,8-Trioxabicyclo[5.1.0]octane Providing an Optically Pure 2-Amino-1,3,4-butanetriol Equivalent.
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)