The first catalytic asymmetric cascade Heck-alkylation
reaction
of NH2-unprotected amino acid esters with N-(2-iodophenyl)allenamides is reported in this work. Under the promotion
of a combining catalytic system comprising a chiral aldehyde, a chiral
palladium complex, and the Lewis acid ZnCl2, the title
reaction takes place smoothly, giving optically active α-alkyl
tryptophan derivatives in moderate to good yields and excellent enantioselectivities.
The target products can be converted into other structurally complex
chiral indoles without the loss of enantioselectivities