Chiral sulfoxides as activators of allyl trichlorosilanes in the stereoselective allylation of aldehydesElectronic supplementary information (ESI) available: General experimental procedures, HPLC, 1H and 13C NMR spectra of new compounds. See DOI: 10.1039/c002988b

Chiral sulfoxides as activators of allyl trichlorosilanes in the stereoselective allylation of aldehydesElectronic supplementary information (ESI) available: General experimental procedures, HPLC, 1H and 13C NMR spectra of new compounds. See DOI: 10.1039/c002988b

Chiral aryl methyl sulfoxides proved to be efficient activators in the asymmetric allylation of aldehydes with allyl trichlorosilanes. High enantioselectivity was found in the case of electron-poor aldehydes. The high levels of diastereoselectivity and the detection of nonlinear effects have allowed...

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description Chiral aryl methyl sulfoxides proved to be efficient activators in the asymmetric allylation of aldehydes with allyl trichlorosilanes. High enantioselectivity was found in the case of electron-poor aldehydes. The high levels of diastereoselectivity and the detection of nonlinear effects have allowed the elucidation of some mechanistic aspects of the reaction. Chiral aryl methyl sulfoxides proved to be efficient activators in the asymmetric allylation of aldehydes with allyl trichlorosilanes. High enantioselectivity was found in the case of electron-poor aldehydes. The high levels of diastereoselectivity and the detection of nonlinear effects have allowed the elucidation of some mechanistic aspects of the reaction.
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title Chiral sulfoxides as activators of allyl trichlorosilanes in the stereoselective allylation of aldehydesElectronic supplementary information (ESI) available: General experimental procedures, HPLC, 1H and 13C NMR spectra of new compounds. See DOI: 10.1039/c002988b
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