Abstract
Regioselective hydrazidohydroxylation of styrenes with N-acetylaminophthalimide using phenyliodine(III) bis(trifluoroacetate) was carried
out to afford 1-aryl-2-(N-acetyl-N-phthalimido)aminoethyl trifluoroacetates in high yields. The procedure is operationally
simple and removal of trifluoroacetyl and phthalimido groups was performed by treatment
of the trifluoroacetate with hydrazine hydrate in good yield. A synthetic study and
a mechanistic proposal for the hydrazidohydroxylation are presented.
Key words
hydrazidohydroxylation - styrene -
N-acetylaminophthalimide - nitrenium ion - phenyliodine(III) bis(trifluoroacetate)
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