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- W1834512944 abstract "The conjugate addition of cis- or trans-1-alkenyl-cuprolithium complexes (RCHCH)2CuLi · Xn1 R alkyl, X ligands such as ether, tetrahydrofuran, (CH3O)3P and (n-Bu)3P. Physical studies to determine the structure of these copper reagents are in progress, see footnote 20 of reference [1]. to α, β-unsaturated carbonyl compounds was found to occur with high retention of double bond geometry, affording isomerically pure cis- or trans-γ, δ-ethylenic carbonyl compounds. The same 1-alkenylcuprates also react stereospecifically with alkyl halides to give isomerically pure cis- or trans-olefins." @default.
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- W1834512944 date "1971-11-01" @default.
- W1834512944 modified "2023-10-15" @default.
- W1834512944 title "Stereospecific Olefin Synthesis<i>via</i>Lithium Vinylcuprates" @default.
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- W1834512944 doi "https://doi.org/10.1002/hlca.19710540722" @default.
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