Abstract
The addition of organometallic reagents to ketones constitutes one of the most straightforward synthetic approaches to tertiary
alcohols. However, due to the absence of a well-behaved class of cyclopropanone surrogates accessible in enantioenriched form, such a trivial
synthetic disconnection has only received very little attention in the literature for the formation of tertiary cyclopropanols. In this work, we
report a simple and high-yielding synthesis 1-substituted cyclopropanols via the addition of diverse organometallic reagents to 1-
phenylsulfonylcyclopropanols, acting here as in situ precursors of the corresponding cyclopropanones.The transformation is shown to be amenable to sp, sp2 or sp3
-hybridized organometallic C-nucleophiles under mild conditions, and the use of enantioenriched substrates led to highly
diastereoselective additions and the formation of optically active cyclopropanols.