A new synthesis of alpha-N-ethylamino acids starting from alpha-amino acids
using hexafluoroacetone as protecting and activating agent is described. T
he hexafluoroacetone-protected N-ethylamino acid derivatives obtained are a
ctivated lactons. Therefore, they can be directly transformed without the n
eed of an additional activation step with various nucleophiles into the cor
responding carboxylic acid derivatives.