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Updated: Jan 27, 2026

One-step Metabolomics: Carbohydrates, Organic and Amino Acids Quantified in a Single Procedure
Published on: June 25, 2010
Access to Unprotected β-Fluoroalkyl β-Amino Acids and Their α-Hydroxy Derivatives
Volodymyr Sukach1,2, Serhii Melnykov3,4, Sylvain Bertho2
1Le Studium Loire Valley Institute for Advanced Studies , 1, rue Dupanloup , Orléans 45000 , France.
Abstract:
Unprotected β-(het)aryl-β-fluoroalkyl β-amino acids and their α-hydroxy derivatives can be readily obtained using a decarboxylative Mannich-type reaction without protection/deprotection steps. This protocol utilizes lithium hexamethyldisilazide and (het)arylfluoroalkyl ketones to generate NH-ketimine intermediates. The mild reaction conditions allow the preparation of original fluorinated β-amino acids as useful building blocks in a practical and scalable manner.
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