Amanote Research
Register
Sign In
Examination of the New A-(2z-Fluoro)vinyl Trigger With Lysine Decarboxylase: The Absolute Stereochemistry Dictates the Reaction Course
doi 10.1021/ja067240k.s001
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Mechanism and Stereochemistry of the 5-Aminolaevulinate Synthetase Reaction
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
The Michael Reaction. Mechanism, Stereochemistry and a Synthetically Useful Modification.
Acta Chemica Scandinavica
L-Lysine Decarboxylase as a Specific Inhibitor of the Growth of a Species of Pichia
Journal of General Microbiology
Cadaverine Production From L-Lysine With Chitin-Binding Protein-Mediated Lysine Decarboxylase Immobilization
Frontiers in Bioengineering and Biotechnology
Bioengineering
Biomedical Engineering
Histology
Biotechnology
Progressive-Convergent Elucidation of Stereochemistry in Complex Polyols. The Absolute Configuration of (-)-Sagittamide A
Absolute Stereochemistry of (-)-Preorixine and Related Compounds.
Chemical and Pharmaceutical Bulletin
Medicine
Drug Discovery
Chemistry
Synthesis and Stereochemistry of (E)-5-(3,4,5,6-Tetrahydropyrid-3-Ylidenemethyl)-2-Furanmethanol, a Product of the Reaction Between D-Glucose and L-Lysine.
Acta Chemica Scandinavica
The Absolute Stereochemical Course of Citric Acid Biosynthesis
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
The Absolute Stereochemistry of Nebularine-Methanol Photoadduct. A Potential Transition-State Analog of Adenosine Deaminase.
Chemical and Pharmaceutical Bulletin
Medicine
Drug Discovery
Chemistry