184850-70-2Relevant academic research and scientific papers
Sulfoxide-Controlled SN2′ Displacements between Cyanocuprates and Epoxy Vinyl Sulfoxides
Marino, Joseph P.,Anna, Laura J.,Fernandez De La Pradilla, Roberto,Martinez, Maria Victoria,Montero, Carlos,Viso, Alma
, p. 6462 - 6473 (2007/10/03)
Two short and convergent routes have been devised for the preparation of enantiomerically pure acyclic epoxy vinyl sulfoxides. These substrates undergo highly regio- and stereoselective SN2′ displacements with lithium cyanocuprates to give α′-alkylated, γ-oxygenated Z α,β-unsaturated sulfoxides in moderate to good yields and with good to excellent diastereoselectivities. The absolute configuration of the newly formed carbon-carbon bond is primarily controlled by the chiral sulfur atom, which in a nonreinforcing situation can override the intrinsic anti tendency of the vinyl oxirane moiety and forces the cuprate to undergo syn addition. The hydroxy vinyl sulfoxide functionality of the resulting adducts should allow for subsequent asymmetric transformations thus enhancing the synthetic usefulness of this methodology.
Sulfoxide-controlled S(N)2' displacements between cyanocuprates and epoxy vinyl sulfoxides
Marino, Joseph P.,Anna, Laura J.,Fernandez De La Pradilla, Roberto,Martinez, Maria Victoria,Montero, Carlos,Viso, Alma
, p. 8031 - 8034 (2007/10/03)
Readily available enantiomerically pure epoxy vinyl sulfoxides, 10-13 and 15 undergo highly regio- and stereoselective S(N)2' displacements with alkyl cyanocuprates. The sulfinyl auxiliary controls the anti-syn stereochemistry of the process.
