Stereoselective Activation of Small Molecules by a Stable Chiral Silene

稳定手性硅烯对小分子的立体选择性活化

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Abstract

The reaction of the dilithium salt of the enantiopure (S)-BINOL (1,1'-bi-2-naphthol) with two equivalents of the amidinate-stabilized chlorosilylene [L(Ph) SiCl] (L(Ph) =PhC(NtBu)(2) ) led to the formation of the first example of a chiral cyclic silene species comprising an (S)-BINOL ligand. The reactivity of the Si=C bond was investigated by reaction with elemental sulfur, CO(2) and HCl. The reaction with S(8) led to a Si=C bond cleavage and concomitantly to a ring-opened product with imine and silanethione functional groups. The reaction with CO(2) resulted in the cleavage of the CO(2) molecule into a carbonyl group and an isolated O atom, while a new stereocenter is formed in a highly selective manner. According to DFT calculations, the [2+2] cycloaddition product is the key intermediate. Further reactivity studies of the chiral cyclic silene with HCl resulted in a stereoselective addition to the Si=C bond, while the fully selective formation of two stereocenters was achieved. The quantitative stereoselective addition of CO(2) and HCl to a Si=C bond is unprecedented.

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