4734-90-1Relevant articles and documents
Copper-catalyzed rearrangement of vinyl oxiranes
Batory, Lindsay A.,McInnis, Christine E.,Njardarson, Jon T.
, p. 16054 - 16055 (2007/10/03)
A novel copper-catalyzed vinyl oxirane ring expansion protocol has been developed. A wide range of vinyl oxiranes can be rearranged to 2,5-dihydrofurans in excellent yields in the presence of electrophilic copper(II) acetylacetonate catalysts. Regioisomeric vinyl oxiranes can be converted to a single dihydrofuran product using these conditions. This method uses low catalyst loadings (0.5-5 mol %), has good tolerance of substitution patterns, and can be done in the absence of solvent. Copyright
Addition of organozinc species to cyclic 1,3-diene monoepoxide
Xue, Song,Li, Yali,Han, Kaizhen,Yin, Wen,Wang, Meng,Guo, Qingxiang
, p. 905 - 907 (2007/10/03)
(equation presented) The reaction of organozinc reagents (ZnEt2, ZnPh2) with cyclic 1,3-diene monoepoxides in the presence of CF3COOH gave the cis-addition products. Lewis acids such as (CF3CO2)2