Paper
An Efficient Synthesis of 3-Amino-4-Fluorobutanoic Acid, an Inactivator of GABA Transaminase
Published Apr 1, 1985 · J. Mathew, B. Invergo, R. Silverman
Synthetic Communications
Q3 SJR score
6
Citations
0
Influential Citations
Abstract
Abstract 3-Amino-4-fluorobutanoic' acid (1), a potent in vivo-inactivator of GABA transaminase, is synthesized in two steps. The lithium salt of tert-butyl acetate is condensed with fluoroacetonitrile and the product is reduced with sodium cyanoborohydride in acidic methanol to 1.
Study Snapshot
3-Amino-4-Fluorobutanoic Acid is a potent in vivo-inactivator of GABA transaminase, with a facile two-step synthesis process.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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References
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The pyridoxal 5-phosphate-dependent enzyme GABA-AT requires HF elimination for inactivation, with aromatization competing with Michael addition mechanism for activation.
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A New Synthesis of 3-Amino-2-alkenoates. Novel Synthetic Route to Amino Sugars N-Benzoyl-L-daunosamine and -L-acosamine
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