Abstract
Aryl- and alkenylsilanediols, which possess two hydroxy groups on the silicon atom,
undergo the rhodium-catalyzed addition of an organic group on silicon to internal
alkynes. Treatment of several internal alkynes with aryl- or alkenylsilanediols in
the presence of 3 mol% of [Rh(OH)(cod)]2 affords the hydroarylated or hydroalkenylated products in good yields. A crucial
role of the hydroxy group of silanediol for the catalytic reaction is also discussed
with the related aryltin reagent.
Key words
silanediol - rhodium complex - hydroarylation - hydroalkenylation - internal alkyne
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