Tritium nmr in investigations of branched-chain amino acid metabolism
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference36 articles.
1. Configuration of α,β-dihydroxy-β-methylvaleric acid, an isoleucine precursor
2. Stereochemistry of valine and isoleucine biosynthesis II. Absolute configuration of (−)α,β-dihydroxyisovaleric acid and (−)α,β-dihydroxy-β-methylvaleric acid
3. Stereoselectivity and stereospecificity of the α,β-dihydroxyacid dehydratase and from Salmonella typhimurium
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1. Stereochemistry of Metabolic Reactions of Amino Acids;Topics in Stereochemistry;2007-02-26
2. The first simple and efficient synthesis of the unusual dipeptide part of Phomopsin A;Tetrahedron: Asymmetry;2005-07
3. Synthesis of [1-13C] and [1-15N] labelled DL-homophenylalanine via a key Neber rearrangement;Journal of Labelled Compounds and Radiopharmaceuticals;1998-01
4. Evidence for an insertion-homolysis mechanism for carbon-sulphur bond formation in penicillin biosynthesis; 1. Synthesis of tripeptide probes;Tetrahedron;1996-02
5. Synthesis of Methyl (Z)- and (E)-2-Methyl-(3-D)propenoates and Their Incorporation Into Polymethacrylates;Australian Journal of Chemistry;1993
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