842169-79-3Relevant articles and documents
Access to Unprotected β-Fluoroalkyl β-Amino Acids and Their α-Hydroxy Derivatives
Sukach, Volodymyr,Melnykov, Serhii,Bertho, Sylvain,DIachenko, Iryna,Retailleau, Pascal,Vovk, Mykhailo,Gillaizeau, Isabelle
, p. 2340 - 2345 (2019)
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.