Transition-Metal-Free Coupling Reaction of Vinylcyclopropanes with Aldehydes Catalyzed by Tin Hydride

Donor–acceptor cyclopropanes are useful building blocks for catalytic cycloaddition reactions with a range of electrophiles to give various cyclic products. In contrast, relatively few methods are available for the synthesis of homoallylic alcohols through coupling of vinylcyclopropanes (VCPs) with aldehydes, even with transition‐metal catalysts. Here, we report that the hydrostannation of vinylcyclopropanes (VCPs) was effectively promoted by dibutyliodotin hydride (Bu2SnIH). The resultant allylic tin compounds reacted easily with aldehydes. Furthermore, the use of Bu2SnIH was effectively catalytic in the presence of hydrosilane as a hydride source, which established a coupling reaction of VCPs with aldehydes for the synthesis of homoallylic alcohols without the use of transition‐metal catalysts. In contrast to conventional catalytic reactions of VCPs, the presented method allowed the use of several VCPs in addition to conventional donor–acceptor cyclopropanes. A tin allyl! The hydrostannation of vinylcyclopropanes (VCPs) was effectively promoted by Bu2SnIH, and the resultant allylic tin compounds reacted easily with aldehydes (see scheme). Furthermore, the use of Bu2SnIH was effectively catalytic, which established a catalytic coupling reaction of VCPs with aldehydes without the use of transition‐metal catalysts. The method allowed the use of VCPs in addition to conventional donor–acceptor cyclopropanes.