Abstract
An
unprecedented copper(I)-catalyzed vinylation of (donor)-acceptor
diazo compounds
with VinylBenziodoXolone reagents (VBX) as partners is reported. The
transformation tolerates variation of both donor- and acceptor substituents on
the diazo compounds, delivering the corresponding benzoylated allylic alcohol
products in good to excellent yields. Through the development of a protocol for
the synthesis of functionalized alkanes-, dienes- and enynes-substituted VBX
reagents, a broad scope of substituents on the alkene could be accessed. The
obtained products contain synthetically versatile functional groups, such as an
aryl iodide, an ester and an allylic leaving group, enabling selective further
modification.