Enantiomerically pure 4-amino-allyloxy-acetates, prepared from L-amino acids, undergo a Stereoselective Wittig rearrangements with formation of the corresponding α-hydroxy-γ-amino acid esters having γ-turn conformational features.
M. T. Reetz, N. Griebenow and R. Goddard, J. Chem. Soc., Chem. Commun., 1995, 1605 DOI: 10.1039/C39950001605
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