Abstract
Abstract Reaction of the cyclic carbonates of acyclic vinyl diols with RCu(CN)Li· BF 3 , RCu(CN)MgBr·BF 3 , or RMgBr·CuI (cat) in THF at −78 °C proceeded in S N 2′ fashion and resulted in the formation of alkylated ( E )-allylic alcohols with remarkably high diastereoselectivity. This reaction represents an efficient 1, 3-chirality transfer method.
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